Despite promising preclinical data supporting the blockage of MMPs as a treatment for cancer, all Phase III cancer trials failed. This might be due to inadequate clinical trial design, the characteristics of the MMP inhibitors used, poor knowledge on the complexity of the MMPs and discrepancies between the mouse models and the patients enrolled in the clinical trials.
Over the past decade, much knowledge has been accumulated on the functions of the different MMPs, and better and more specific MMP inhibitors have been developed. So far, however, this has not resulted in MMP inhibitors that are ready for clinical use.
The reluctance to therapeutically inhibit MMPs has been influenced by the failure of the first clinical trials and the observed side effects, the complexity of the MMPs that exert both detrimental and beneficial roles and the lack of tools to dissect the role of a specific MMP in a specific organ. In addition, the high homology between the MMPs, the difficulty in identifying substrate specificity and the discrepancy between in vitro and in vivo identified substrates impede the development of specific MMP inhibitors.
Nevertheless, many data are available from studies of MMP-knockout mice and on the use of MMP inhibitors in animals that support therapeutic MMP inhibition in inflammatory conditions such as systemic inflammatory response syndrome (SIRS), sepsis and disorders associated with intestinal and brain inflammation.
Based on the currently available data, MMP inhibition has great therapeutic potential for the treatment of inflammatory disorders. However, this can only be fully explored once the MMP functions are unravelled in more detail and potent and selective MMP inhibitors are available.
Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that form a family of 24 members in mammals. Evidence of the pathological roles of MMPs in various diseases, combined with their druggability, has made them attractive therapeutic targets. Initial drug discovery efforts focused on the roles of MMPs in cancer progression, and more than 50 MMP inhibitors have been investigated in clinical trials in various cancers. However, all of these trials failed. Reasons for failure include the lack of inhibitor specificity and insufficient knowledge about the complexity of the disease biology. MMPs are also known to be involved in several inflammatory processes, and there are new therapeutic opportunities for MMP inhibitors to treat such diseases. In this Review, we discuss the recent advances made in understanding the role of MMPs in inflammatory diseases and the therapeutic potential of MMP inhibition in those conditions.
Until approximately 15 years ago, matrix metalloproteinases (MMPs; also known as matrixins) were mainly known for their role in promoting cancer progression. Their ability to degrade connective tissue between cells and in the lining of blood vessels enables tumour cells to escape from their original location and seed metastases1. This knowledge prompted the development of the first generation of broad-spectrum synthetic inhibitors that block MMP activity by binding to the Zn2+ ion in their active sites. Preclinical studies using these inhibitors (such as batimistat (also known as BB-94)2) indicated that they had strong potential as anticancer agents1. Consequently, more than 50 MMP inhibitors were investigated in clinical trials. Surprisingly, despite the wealth of preclinical data supporting the use of MMP inhibitors as anticancer drugs, all of these trials failed. There are several explanations for these failures (Box 1), including problems associated with the clinical trial itself (such as poor trial design and the use of inadequate clinical end points) and with the MMP inhibitors themselves (such as metabolic instability, poor oral bioavailability and dose-limiting toxicities). Moreover, poor knowledge of the complexity of MMP function and of the targeted MMPs, together with the use of broad-spectrum MMP inhibitors, resulted in some MMP agents inhibiting antitarget MMPs3,4,5,6,7,8,9,10,11.
While clinical trials with various MMP inhibitors were ongoing, new information regarding the role of MMPs was being uncovered, and the full story turned out to be more complex than previously thought. The idea that all MMPs promote the development of cancer was a misconception because not every MMP had been identified when the first clinical trials started. It subsequently became clear that not all MMPs need to be blocked in all cases and at all times12. Indeed, depending on their substrates, MMPs can have opposing effects on central aspects of tumour progression, such as tumour growth and survival, angiogenesis, invasion and modulation of the immune response13,14,15. In addition to their functions as tissue-remodelling enzymes, MMPs are also processing enzymes that selectively cleave many non-matrix targets, such as cell surface receptors, cytokines, chemokines, cell–cell adhesion molecules, clotting factors and other proteinases16.
Early clinical trials with broad-spectrum MMP inhibitors also revealed that prolonged treatment causes unwanted side effects, particularly musculoskeletal pain and inflammation17,18. These effects were reversible, but in subsequent trials the dose was reduced to avoid these inadvertent effects. Consequently, MMP inhibitor doses were often inadequate to affect tumour biology and combination therapies were never considered. Most worryingly, two trials involving the MMP inhibitor tanomastat in small-cell lung cancer and pancreatic cancer had to be halted prematurely as patients receiving the inhibitor showed significantly shorter survival than patients receiving placebo3. These undesired side effects were most probably due to the broad-spectrum inhibition of MMPs, as well as the cross-inhibition of a disintegrin and metalloproteinase (ADAM) family members and of aggrecanases (ADAMs with thrombospondin motifs (ADAMTS) family members). ADAMs and aggrecanases are considered to be involved in important cellular events, such as cellular adhesion, mediation of cell–matrix interactions, regulation of growth factor availability and membrane protein shedding19,20.
Another possible reason for the clinical trial failures is the lack of applicability of the mouse models to the patients enrolled in the clinical trials. That is, patients in the trials were often in advanced stages of disease, whereas in the animal studies MMP inhibitors in were effective in early stages of the disease.
Despite these disappointments, we and others think that inhibiting MMP activity is still a rational therapeutic approach, particularly for inflammatory disorders in which MMPs often activate or overactivate signal transduction pathways that control cytokine biosynthesis and direct systemic inflammation or barrier immunity21. In this Review, after describing the basic aspects of MMPs, their natural inhibitors and the advances made in optimizing the available MMP inhibitors, we provide an overview of the therapeutic potential of MMP inhibition in inflammatory diseases. We focus on systemic inflammatory response syndrome (SIRS), sepsis and disorders linked with intestinal and brain inflammation, discussing results from knockout and inhibitor studies in rodents. Finally, we reflect on the future prospects of developing therapeutic MMP inhibitors.
Basic aspects of MMP biology
MMP activity was discovered in 1962 in tadpoles, in which a molecule with collagenolytic activity was shown to degrade extracellular matrix (ECM) proteins in the tails, which is a necessary process for metamorphosis22. MMPs belong to the metzincin superfamily of metalloproteinases (Fig. 1). MMPs are multidomain proteins with globular catalytic domains that are approximately 130–260 residues in length and have a common core architecture that is characterized by a long zinc-binding consensus motif, HEXXHXXGXX(H/D) and a methionine-containing Met-turn. According to their structural characteristics, metzincins are primarily subdivided into astacins (including the meprins and bone morphogenetic protein 1 (BMP1) and/or Tolloids), adamlysins (including ADAMs and ADAMTSs), pappalysins, bacterial serralysins and MMPs23. The catalytic domain of all MMPs contains a Zn2+ ion that is coordinated by a tris(histidine) motif followed by a conserved methionine residue. So far, the MMP family comprises 24 structurally and functionally related members in mammals (Fig. 1; see Supplementary information S1 (table)).
MMPs typically have an amino-terminal signal peptide (pre-domain) to target the enzyme to the endoplasmic reticulum and transport it out of the cell. Next, there is a conserved pro-domain containing a consensus cysteine-switch sequence that shields the neighbouring catalytic domain, which contains a zinc-binding consensus sequence. At the carboxy-terminal end, most MMPs have a haemopexin-like domain that modulates substrate recognition and is connected to the catalytic domain by a flexible hinge region.
MMPs are synthesized as enzymatically inactive zymogens (pro-MMPs) that are activated by the 'cysteine switch', which disrupts the interaction between a cysteine in the pro-domain and the Zn2+ ion in the active site. Proteolytic removal of a bait region in the pro-domain by serine proteinases, furin or other MMPs destabilizes the pro-peptide and disrupts the Zn2+–cysteine interaction. Alternatively, the Zn2+–cysteine interaction can be disrupted through modification of the thiol group of the cysteine with physiological agents (for example, oxidants and disulphides) or non-physiological agents (for example, alkylating compounds and heavy metal ions), as well as through allosteric perturbation of the zymogen, which can lead to irreversible activation of the MMP by autolysis24.
The MMPs can be classified in different ways. The most commonly used classification is partly based on historical assessment of the substrate specificity of the MMP and partly based on the cellular localization of the MMP. According to these criteria, these groups are the collagenases, the gelatinases, the stromelysins and the membrane-type MMPs (MT-MMPs). However, several MMPs do not fit into any of these traditional groups.
Alternatively, MMPs can be classified on the basis of their domain organization as archetypal MMPs, matrilysins, gelatinases or furin-activatable MMPs25 (Fig. 1). Archetypal MMPs can be further subdivided into three subgroups on the basis of their substrate specificity: collagenases, stromelysins and 'other'. Collagenases (MMP1, MMP8, MMP13 and also MMP18 in Xenopus spp.) can process the collagen triple helix. Stromelysins (MMP3 and MMP10) have the same structural design as collagenases but cannot degrade native collagen, although they can activate several pro-MMPs. Four other archetypal MMPs (MMP12, MMP19, MMP20 and MMP27) cannot be classified as collagenases or stromelysins. There are only two matrilysins (MMP7 and MMP26), and these are characterized by the absence of a haemopexin domain. The gelatinases (MMP2 and MMP9) have a fibronectin type II motif located inside their catalytic domain, which enables them to bind and degrade gelatin (denatured collagen). As their name suggests, furin-activatable MMPs can be activated intracellularly by furin-like proteases owing to the furin recognition motif located between the pro-peptide and the catalytic domain. Three furin-activatable MMPs are secreted after activation: MMP11, MMP21 and MMP28. The other furin-activatable MMPs have membrane-anchoring domains that localize them at the cell surface, where they control the pericellular environment. They are anchored to the plasma membrane by a glycosylphospatidylinositol anchor (MMP17 (also known as MT4-MMP) and MMP25 (also known as MT6-MMP)) or by an extensive hydrophobic site in type I transmembrane MMPs (MMP14 (also known as MT1-MMP), MMP15 (also known as MT2-MMP), MMP16 (also known as MT3-MMP) and MMP24 (also known as MT5-MMP)). MMP23A and MMP23B (originally named MMP22) have unique features: they lack the conserved signal peptide, the cysteine-switch motif and the haemopexin domain, but they contain a cysteine array, an immunoglobulin domain and an N-terminal type II transmembrane domain.
MMPs are important regulators of cellular activities. They collectively degrade structural components of the ECM and thereby influence several physiological processes, including reproduction, embryogenesis, angiogenesis and tissue remodelling; ECM degradation facilitates cell migration and the release of bound signalling molecules, such as chemokines, cytokines and growth factors26,27. In addition, it has become widely accepted that MMPs also have a central role in the direct activation of signalling molecules, such as tumour necrosis factor (TNF) and other cytokines; MMPs therefore also contribute to various aspects of immunity21,28. MMP activity is almost undetectable under normal physiological conditions but can be observed during certain biological processes such as angiogenesis, bone development, wound healing and mammary involution29. Owing to their destructive properties, they are tightly regulated at the levels of transcription, proteolytic activation of the zymogen, interaction with, and retention by, specific ECM components and inhibition by endogenous inhibitors, such as α2-macroglobulin and tissue inhibitors of metalloproteinases (TIMPs)30.
TIMPs are 21–28 kDa proteins that bind and reversibly block MMP activity21. Four TIMPs have been characterized and are either anchored to the ECM or secreted in a soluble form31,32. TIMPs consist of a C-terminal domain and an N-terminal domain that each contain three conserved disulphide bonds. The N-terminal domain folds within itself and binds to the active site of MMPs to inhibit their activity33. The TIMPs are highly similar in structure but have markedly different expression patterns; TIMP expression responds to various physiological stimuli in diverse cell types, comparable to MMP expression21. TIMP1, TIMP2 and TIMP3 are widely expressed in many mammalian tissues, whereas TIMP4 is expressed in specific tissues34. TIMP1 is also expressed in specific regions of the brain, and TIMP3 is particularly expressed in the basement membranes of the eye and kidney34. TIMP4 expression is restricted to tissues such as the heart, kidney, ovary, pancreas, colon, testes, brain and adipose tissue34. Although there is considerable overlap in the MMPs that they target, there is some specificity: TIMP2, TIMP3 and TIMP4 inhibit all MMPs, whereas TIMP1 inhibits all MMPs except MT1-MMP, MT2-MMP, MT3-MMP and MT5-MMP32. In addition, TIMP3 inhibits several ADAM and ADAMTS family members and TIMP1 inhibits ADAM10 (Ref. 32). Mice deficient in TIMP1, TIMP2 or TIMP4 have no obvious abnormalities, whereas mice deficient in TIMP3 have lung emphysema-like alveolar damage, more rapid apoptosis of mammary epithelial cells after weaning, chronic hepatic inflammation and failure of liver regeneration35,36,37.
Although there is a degree of substrate redundancy among MMPs, there is clearly an important selective pressure to conserve all MMP family members during mammalian evolution, which suggests that each MMP has specific and important functions. The availability of MMP-deficient mice has therefore been of great value in understanding their functions in several physiological processes and pathologies and in predicting the effects of potential inhibitors that target specific MMPs.
MMP inhibitor development
Hydroxamate-based inhibitors. Initial efforts to develop MMP inhibitors primarily focused on compounds containing a group that chelated the catalytic Zn2+ ion and a backbone designed to mimic the natural peptide substrate of the desired MMP or MMPs. The first-generation MMP inhibitors were based on the structure of collagen. These inhibitors comprised the basic backbone of collagen and the zinc-binding group hydroxamate (−CONHOH)38, and they were consequently called hydroxamate-based MMP inhibitors (Table 1). Hydroxamate is a highly potent ligand that binds to the catalytic Zn2+ ion of the enzyme to create a distorted trigonal–bipyramidal geometry around the Zn2+ ion. In addition, the −NH group of the hydroxamate anion forms a short but strong hydrogen bond with the neighbouring carbonyl oxygen, and hydrophobic contacts stabilize the inhibitor–enzyme complex39. These strong Zn2+-chelating moieties reduce the contribution of the rest of the compound to the inhibitor–enzyme binding process, thereby favouring broad-spectrum inhibition6. Examples of collagen-based peptidomimetic hydroxamates include marimastat, ilomastat (also known as GM6001) and batimastat. Batimastat is a low-molecular-mass hydroxamate derivative with low water solubility and was the first MMP inhibitor to enter clinical trials40. It inhibits several MMPs, including MMP1, MMP2, MMP7 and MMP9, by directly binding to Zn2+ ions in the active site41. Several studies demonstrated promising antitumour effects of batimastat in animal models of human ovarian cancer xenografts, colorectal cancer, mouse melanoma and haemangioma42,43,44,45,46,47.
Several clinical studies of hydroxamate-based inhibitors were then conducted9,48,49, but the clinical performance of these compounds was disappointing. For example, marimastat was ineffective at doses already associated with musculoskeletal toxicity in a randomized Phase III trial for metastatic breast cancer that was stable or responding after first-line chemotherapy50. A Phase I trial of marimastat combined with carboplatin and paclitaxel as a therapy against advanced non-small cell lung cancer was also linked to musculoskeletal toxicity, but patients did have a partial response51. Many factors contributed to the disappointing results, including the metabolically labile nature of the hydroxamate zinc-binding group and the serious side effects (such as musculoskeletal pain) experienced by patients taking these inhibitors. The musculoskeletal pain is now thought to be caused by the inhibition of non-MMP metalloproteinases, such as ADAM and ADAMTS family members, including ADAM17 (also known as TACE)52. In addition, hydroxamate-based inhibitors are broad-spectrum inhibitors of many MMP subtypes, and at that time it became clear that MMPs affect many more than the five tumour-associated processes identified thus far (that is, metastasis, tumour growth, angiogenesis, apoptosis and immune modulation)53. Unfortunately, this knowledge was not integrated into the ongoing clinical studies at that time. Moreover, it became clear that optimal clinical performance of the MMP inhibitors depended on administering the inhibitors during the critical MMP enzymatic event in the particular cancer, and this seemed to be early in the metastatic process48,53. Consequently, MMP inhibitors were often administered too late to make a difference54.
Subsequently, a new generation of hydroxamate-based MMP inhibitors was developed, and these consisted of a substituted aryl, a sulphonamide and a hydroxamate zinc-binding group. Examples include MMI-270, which is an orally available and water-soluble low-molecular-mass broad-spectrum inhibitor55, and MMI-166, which is a selective inhibitor of MMP2, MMP9 and MMP14 (Ref. 303). Other hydroxamate-based MMP inhibitors, such as ABT-770, PD-166793 and prinomastat, were developed to avoid binding to the 'shallow pocket' of MMP1, based on the idea, at that time, that MMP1-sparing inhibitors would not induce musculoskeletal toxicity56. Cipemastat (also known as Ro 32–3555), an MMP1, MMP3 and MMP9 inhibitor, was used for the treatment of rheumatoid and osteoarthritis, but its clinical trial was terminated prematurely because it did not prevent progression of joint damage in patients with rheumatoid arthritis57. In addition, a recurring limitation to these hydroxamates is that drug metabolism leads to the loss of the hydroxamate zinc-binding group.
Despite these disappointments, there is still interest in the design and development of hydroxamic acid derivatives, mainly because these compounds are the strongest available MMP inhibitors39. Indeed, new hydroxamate inhibitors are being developed using structure–activity relationship (SAR) analysis, which can help to identify molecular substructures related to the presence or absence of biological activity58. Moreover, quantitative SAR (QSAR) analysis is being used to predict the biological activity of new and untested compounds and even to forecast compounds from the knowledge of their molecular structures59.
Non-hydroxamate MMP inhibitors. Hydroxamic acids are often metabolically labile but there are several other zinc-binding groups that are stable. Reverse hydroxamates and non-hydroxamate inhibitors — for example, carboxylates, hydrocarboxylates, sulphydryls, phosphoric acid derivatives and hydantoins — were developed to avoid the limitations associated with the first-generation MMP inhibitors, such as metabolic inactivation and chelation of metals of other metalloproteins. In addition, once the structure of MMPs was revealed by crystallography, next-generation MMP inhibitors were no longer limited to substrate-like compounds, and new inhibitors were designed with various peptidomimetic and non-peptidomimetic backbone structures60. Numerous backbones were investigated, and they improved with increased knowledge of MMP structure and function.
Rebimastat (also known as BMS-275291), which was one of the earliest non-hydroxamate MMP inhibitors developed, contains a thiol zinc-binding group and is a broad-spectrum MMP inhibitor. The structural scaffold of the thiol of rebimastat is a deep-pocket-binding, non-peptide mimetic and it was constructed to have sheddase-sparing activity, thus preventing inhibition of metalloproteinases that induce the release of TNF, TNF receptor 2, L-selectin, interleukin-1 (IL-1) receptor type 2, and IL-6 receptor61. However, a Phase II trial in early-stage breast cancer and a Phase III trial in non-small cell lung carcinoma both still revealed adverse effects62,63.
Tanomastat, which contains a thioether zinc-binding group and a biphenyl deep-pocket-binding segment, had good tolerance, but efficacy was variable and contradictory outcomes were obtained depending on the timing of administration64. The experience with tanomastat highlights the difficulties with respect to dosing and timing in relation to disease progression.
The thiol-based inhibitor SB-3CT contains a diphenylether deep-pocket-binding scaffold and is a competitive, mechanism-based inhibitor that is specific for MMP2 and MMP9 (Ref 65). Mechanism-based MMP inhibitors bind to the active site of MMPs, resulting in a covalent enzyme modification. This strategy was also used to develop a mechanism-based inhibitor exclusively for MMP2 (Refs 66,67).
The orally bioavailable pyrimidine-based inhibitor Ro 28–2653 inhibits MT1-MMP (also known as MMP14), MT3-MMP (also known as MMP16), MMP2, MMP8 and MMP9 but spares MMP1 and ADAM17 activity5,68. Despite several promising animal studies that demonstrated antitumour and anti-angiogenic activity69,70,71,72, the inhibitor did not progress to clinical trials.
Potent MMP12 inhibitors and MMP13 inhibitors were developed when using the alternative zinc-binding group hydantoin73. In addition, several biphenyl sulphonamide carboxylate MMP inhibitors were designed for the treatment of osteoarthritis and have remarkable selectivity for MMP13 (Refs 74,75,76).
Phosphorous-based MMP inhibitors are structural mimics of the tetrahedral transition state of amide hydrolysis, in which the phosphinic group is the zinc-binding group77. Modulation of R1 and R2 substituents enabled optimization such that potency reached the nanomolar range77. This approach was particularly successful for the development of MMP13 phosphinates; for example, 582311-81-7 (Ref. 78). Similarly, MMP11-selective phosphinate inhibitors, such as RXP-03, were developed; however, the efficacy of RXP-03 was dose-dependent and treatment schedule-dependent79, which again highlights the importance of carefully defining the spatiotemporal function of the targeted MMP.
Tetracycline antibiotics, such as minocycline and doxycycline, have innate MMP inhibitory capacity. The tetracycline analogue doxycycline hyclate is indicated for periodontal disease and is the only collagenase inhibitor approved by the US Food and Drug Administration for any human disease80. The chemically modified tetracycline metastat (also known as COL-3) was tested in a Phase I clinical trial and induced disease stabilization in patients who had a nonepithelial type of malignancy81.
Targeting alternative binding sites. To avoid broad MMP inhibition owing to the high structural homology of the different MMPs and to reduce the off-target effects observed in clinical trials, recent research has switched from targeting the catalytic site to alternative, less conserved sites. Indeed, in addition to the Zn2+ ion in their catalytic site, MMPs possess subsites (S) designated as unprimed (left-hand side of the Zn2+ ion; S1, S2 and S3) or primed (right-hand side of the Zn2+ ion; S1′, S2′ and S3′)82 (Fig. 2). The S1′ pocket is the main subsite for substrate recognition and is the most variable subsite among the different MMPs in terms of the amino acid sequence and the depth of the pocket. MMPs can be classified, on the basis of the depth of this pocket, into shallow, intermediate and deep-pocket MMPs60,83,84. The P1′–S1′ interaction (P1 is the group in the inhibitor or substrate that binds to the S1′ pocket of the enzyme) is the main determinant of the affinity of inhibitors and the cleavage position of peptide substrates85,86. For example, extending the P1 substituent was used to gain MMP13 selectivity over the highly homologous MMP2, taking advantage of the steric limitations of the shorter S1′ loop of MMP2 (Ref 74).
The use of X-ray crystallography and NMR methods combined with computational methods enables the modelling of drug–protein interactions with non-hydroxamate inhibitors of MMPs that bind to sites other than the catalytic site. This makes it possible to design compounds with greater potency and selectivity; indeed, inhibitors with up to three orders of magnitude stronger inhibition capacity of target MMPs compared with non-target MMPs have been developed6. Several of these inhibitors demonstrated impressive MMP13 selectivity, bind deep within the S1′ pocket and resulted in reduced clinical symptoms when tested in mouse models of rheumatoid arthritis and osteoarthritis87,88. Indeed, a co-crystal structure of a highly specific MMP13 inhibitor with the catalytic domain of MMP13 revealed a non-zinc binding mode that relies solely on interactions between the inhibitor and the S1′ binding pocket89.
Similarly, an integrated computational and experimental approach that takes into consideration the structural differences of the S1′ pocket enabled improvement of selectivity in the inhibition of MMP2 over that of MMP9 (Ref. 90). Analogues of a low-micromolar lead MMP13 inhibitor discovered through high-throughput screening were synthesized to investigate SARs, and this resulted in an MMP13 inhibitor that did not seem to bind to the S1′ pocket but to exosites91. These exosites are located outside the substrate-binding pocket but are not yet identified.
It is still a challenge to identify alternative MMP-specific regulatory sites as they are often hidden and scattered over different locations on the surface of the protein. Combining structural spectroscopic analyses, NMR and protein crystallography with computational prediction of effector binding sites revealed these hidden sites, which can be exploited for the rational design of novel molecular effectors and therapeutic agents92.
Peptide-based MMP inhibitors often interact with secondary binding sites on MMPs and inhibitors have been designed that combine peptide-based inhibitors with conventional zinc-binding groups or alternatives93. Phage display peptide libraries have also been used to identify selective MMP2, MMP9 and MT1-MMP inhibitors that were effective in vivo94,95.
Antibody-based therapeutics. Recent research has also focused on the use of functional blocking antibodies, which have high selectivity and potency. Several functional blocking antibodies have been developed that selectively target the membrane-anchored MMPs96. Combining a human antibody phage display library with automated selection and screening strategies97 resulted in the identification of a highly selective antibody-based MMP14 inhibitor called DX-2400. DX-2400 displayed anti-invasive, antitumour and anti-angiogenic properties and blocked MMP14-dependent pro-MMP2 processing98.
Other groups developed selective MMP14 inhibitory antibodies that were successfully tested in vitro and in vivo99,100,101. The neutralizing monoclonal antibody REGA-3G12 was described as a selective inhibitor of MMP9 (Ref. 102); REGA-3G12 is directed against the catalytic domain but not against the fibronectin or zinc-binding domains103. Interestingly, the use of functional blocking antibodies often enables inhibition of specific functions of the MMP rather than its general proteolytic activity. For example, the mouse 9E8 monoclonal antibody targets only the MMP2-activating function of cellular MT1–MMP rather than the general proteolytic activity or the pro-migratory function of this MMP104.
Another proposed strategy for generating inhibitory antibodies that effectively target the in vivo activity of dysregulated metalloproteinases is mimicking the mechanism used by TIMPs105. Based on the three-dimensional structure and amino acid sequence of MMP13, a neutralizing antibody was developed that bound to the active form of MMP13 but not to the latent form or to other MMPs106. Another monoclonal antibody against MMP2 inhibited its activity but did not affect the closely related MMP9 (Ref. 107); however, no other cross-reactivity was investigated with this antibody.
Endogenous inhibitors of MMP function. Several groups have focused on the use of endogenous MMP inhibitors as therapeutics, such as α2-macroglobulin and TIMPs34. α2-macroglobulin is a large serum protein that only partly regulates MMP activity. MMPs are entrapped within the macroglobulin, thus preventing the MMP from accessing large substrates108. In addition, this complex is endocytosed and cleared by a low-density lipoprotein receptor-related protein109. Both chemically modified and polymyxin B-conjugated α2-macroglobulin demonstrated protective effects in mouse models of sepsis110,111. However, this was linked to its binding to, and neutralization of, inflammatory cytokines and MMP inhibition was not studied.
Although TIMPs could theoretically form the basis of another novel class of MMP inhibitors, they have rarely been considered34 and it is unlikely that they will be used therapeutically. Until now, they have only been used in model systems to yield vital clues about the efficacy of metalloproteinase inhibitors in the abrogation of disease112,113. In light of this, it is important to note that the idea that TIMPs only inhibit MMPs is a misconception, as several MMP-independent effects of TIMPs have been described114,115,116. For example, TIMP2 exerted anti-angiogenic effects via binding with integrin α3β1 (Refs 117,118). Moreover, domain-specific overexpression of TIMP2 and TIMP3 revealed MMP-independent functions of TIMPs during development119. It also seems extremely difficult to control the protease/antiprotease balance and, consequently, the net MMP activity. Moreover, in specific cases, TIMPs can even indirectly promote MMP activity120.
MMPs in inflammatory diseases
Despite the disappointing results from clinical trials of MMP inhibitors in oncology, there is increasing experimental evidence that selective MMP inhibition might lead to new therapies for inflammatory disorders121,122,123,124,125,126,127. MMPs are a crucial component of immune cell development and function, as has been reviewed in detail elsewhere21,128. Here, we discuss the recent advances achieved using MMP inhibitors and genetically modified mice in unravelling the roles of specific MMPs in inflammatory diseases such as sepsis and inflammation of the gut and brain. The importance of MMPs and MMP inhibition in lung diseases123, ischaemia–reperfusion124, periodontal inflammation80 and vascular pathologies125,126,127 has been recently reviewed elsewhere.
MMPs in SIRS and sepsis. Sepsis, severe sepsis and septic shock are escalating forms of SIRS initiated by an infection. According to recent estimates, the annual incidence of SIRS is ~19 million cases worldwide, but the actual number is probably much higher129. Overall, sepsis causes ~20–30% mortality, which makes its treatment an urgent clinical need. Apart from antibiotics, the treatment of sepsis is mainly supportive care of organ functions. Many clinical trials of sepsis therapies have failed over the past decades, and the recent withdrawal of activated protein C from the market by Eli Lilly and Company130 and the decision to stop further clinical trials of CytoFab (AstraZeneca/BTG), which is a polyclonal TNF-specific antibody, illustrate the magnitude of the problem.
Treatment of sepsis is challenging owing to the complexity of the disease, which is at three levels: the patient (age, gender, genetic background, risk factors and other diseases); the microbial agent (bacteria, viruses and fungi); and the complexity of the host response. Regarding the host response, patients with SIRS clearly show both an inflammatory and an immune-suppressive profile. Hence, it is not always clear whether inflammation should be blocked or immune suppression should be reverted as patients need an immune response to deal with the infection129. Therefore, partial or local inhibition of inflammatory mediators or pathways may decrease inflammation while maintaining an appropriate level of immune activation, as was recently shown by using very low dose glucocorticoids in a mouse model131.
Apart from inflammation, other complex processes are also activated during sepsis, such as the complement system, coagulation and fibrinolysis. Furthermore, the failure of clinical trials should be interpreted in the light of the substantial differences in genomic responses in leukocytes (one of many important immune cell types) between humans and mice, indicating that mice are suboptimal for preclinical studies of sepsis132. There are many arguments against this point of view, but the discussion illustrates a strong concern that our current models cannot accurately predict the outcome of new investigative therapies.
Several mouse models of sepsis are used in studies, such as endotoxaemia (a form of septic shock caused by the injection of bacterial lipopolysaccharides), kidney ischaemia–reperfusion, and cecal ligation and puncture (CLP). Of all of these models, CLP is recognized as the gold standard mouse sepsis model, in which live bacteria stimulate the host via several pathways, including endotoxins released by the bacteria133. Injection of high doses of bacteria into mice is not a valid sepsis model for MMP research as bacterial proteases might activate MMPs134, so the data from these experiments could be misleading.
Our current understanding of sepsis suggests that development of successful therapeutic strategies must address the activation of multiple pathways during sepsis (inflammation, coagulation, fibrinolysis and complement)129. Notably, sepsis treatment is short-term, and so the toxicity profiles of these drugs do not have to be as 'clean' as they do for long-term treatments. Interestingly, several MMPs are simultaneously biologically active in several of these multiple pathways, making MMPs interesting therapeutic candidates for sepsis treatment122 (Fig. 3).
It has long been known that the expression of many MMP family members is enhanced in endotoxaemia135,136,137, and studies using MMP inhibitors and MMP-knockout mice indicate that MMPs have essential roles in infection and in host defence138,139 (Table 2). Broad-spectrum MMP inhibition by GM6001 decreased CLP-induced neutrophil expression of macrophage receptor 1 (MAC1; also known as integrin αM), the production of CXC chemokines, oedema and neutrophil infiltration in the lung140. Similarly, in CLP-induced septic rats, the chemically modified tetracycline COL-3 (which is a broad-spectrum MMP inhibitor) had reduced toxicity and a reduced ability to cross the blood–brain barrier (BBB)141,142, which led to reduced sepsis-induced lung injury and improved survival143.
Many researchers initially focused on MMP9 as a therapeutic target144, as its expression is increased in patients with septic shock145 as well as in animal models of endotoxaemia and CLP-induced sepsis146. MMP9-deficient mice were protected against lipopolysaccharide-induced lethality137, and use of an MMP9 chemical inhibitor that also inhibits MMP8 and ADAM17 confirmed the protective effect of MMP9 inhibition in endotoxaemia147. In the CLP-induced sepsis model, MMP9-deficient mice were hypersensitive to CLP-induced sepsis148; however, MMP9 inhibition in rats protected them from CLP-induced BBB dysfunction149. These results illustrate that the endotoxaemia model may not be a suitable model to evaluate sepsis therapeutics as it is fundamentally a model of acute inflammation and lacks the contribution of living bacteria. Moreover, these data also highlight the different outcomes from studies using knockout mice (which lack the gene, the function of which can be compensated by other gene products) compared with studies using inhibitors (which may lack specificity and sufficient bioavailability). Indeed, the endotoxin model does not adequately mimic clinical sepsis as it lacks an infectious source from which bacteria invade the host and cause SIRS. Additionally, this research illustrates that in sepsis, certain MMPs may be antitargets rather than therapeutic targets.
Over the past 3 years, promising breakthroughs have been achieved and the roles of a few MMPs in mouse sepsis models have been discovered. In 2011, Tressel et al.150 reported that circulating levels of MMP1 (also known as collagenase 1) are increased in patients with sepsis and that higher levels of active MMP1 directly correlate with lower rates of survival in these patients. In the CLP-induced sepsis model, MMP1A was released from endothelial cells and detected in the circulation shortly after onset of inflammation. A chemical MMP inhibitor that blocks MMP1 and MMP8 protected mice from CLP-induced lethality, and protection was also obtained using an MMP1-specific antibody. The mechanism by which MMP1 contributes to sepsis is thought to be at the level of coagulation as it was observed that MMP1 is the protein that is primarily responsible for the activation of protease-activated receptor 1 (PAR1), an endothelial transmembrane protein that is responsive to the clotting protease thrombin. Interestingly, PAR1 is also the therapeutic target of activated protein C. Cleavage of PAR1 leads to inflammation and endothelial dysfunction, which is a hallmark of sepsis151. Although therapeutic MMP1 inhibition protected wild-type mice from CLP-induced lethality and reduced lung vascular permeability, clotting abnormalities and cytokine production, it did not protect PAR1-deficient mice from CLP-induced lethality, which suggests that the activities of MMP1 are strictly PAR1-mediated152. However, PAR1-deficient mice were not resistant to CLP-induced lethality and survival rates became significantly worse when the MMP1 inhibitor was administered in the advanced stage of disease, suggesting that MMP1 (and hence PAR1) inhibition at later stages is not desirable. Notably, MMP1A-deficient mice do not show any abnormalities153, but MMP1 is one of the MMPs implicated in the MMP inhibitor-associated musculoskeletal pain syndrome. It would therefore be interesting to test whether treatment with an MMP1-specific antibody induces musculoskeletal pain.
A second MMP that has therapeutic potential in sepsis is MMP8 (also known as collagenase 2), which is expressed by many cell types and has several potential substrates154,155. In 2007, Tester et al.156 reported that MMP8-deficient mice did not mount an inflammatory response in a model of local lipopolysaccharide-induced inflammation; MMP8 normally activates an inflammatory chemokine called LIX. Interestingly, two groups described a direct association between MMP8 serum levels and mortality in sepsis patients157,158. It has been proposed that MMP8 could be a potential biomarker for sepsis, to be used alongside MMP1 and the previously reported MMPs, MMP3 (Ref. 159), MMP9 and MMP10 (Ref. 160). Moreover, the crucial role for MMP8 in sepsis indicated by these results was confirmed in studies demonstrating that MMP8-deficient mice were resistant to different types of induced sepsis. Solan et al.158 induced sepsis via CLP in MMP8-deficient mice and presented arguments for activation of nuclear factor-κB (NF-κB) by MMP8 (Ref. 158). Consistent with these results, we found that MMP8-deficient mice were highly resistant to the lethal effects of endotoxaemia, CLP and kidney ischaemia–reperfusion and that an MMP8 chemical inhibitor elicited similar effects161. We linked this resistance to MMP8-dependent collagen degradation that causes increased leakage of the blood–cerebrospinal fluid barrier (a single layer of choroid plexus epithelial cells that forms a tight barrier between the blood and the brain)161. However, not all groups have found reduced inflammatory responses to endotoxin in MMP8-deficient mice; for example, in one study, MMP8 deficiency promoted a lung inflammatory response during endotoxaemia via the modulation of S100A8 and S100A9 (Ref. 162). This result provides a reminder that endotoxaemia and sepsis are the consequences of complex host responses involving pathways that may be stimulated or inhibited by a given MMP.
Another MMP that has recently been recognized as important in sepsis is MMP13 (also known as collagenase 3), which has been extensively investigated in several inflammatory conditions, particularly arthritis163 and wound healing164. This resulted in the development of selective MMP13 inhibitors165. MMP13 transcription is increased in response to inflammation through NF-κB and mitogen-activated protein kinase (MAPK)-regulated elements in its promoter166,167. However, anti-inflammatory glucocorticoids also increase MMP13 transcription in a manner that is dependent on the activator protein 1 binding site in the MMP13 promoter168. We have shown that MMP13-deficient mice were resistant to endotoxaemia and CLP-induced sepsis169. These data are consistent with the idea that the gut is the driving force in sepsis and that MMP13 controls sepsis-promoting factors in the gut170,171. This hypothesis states that the gut epithelium, which is one-cell-layer thick and covered on the luminal side by a mucus layer that prevents direct contact with microorganisms from the gut, forms an important barrier that becomes permeable in sepsis. This permeability leads to life-threatening traffic of gut microbiota, pathogen-associated molecular patterns and danger-associated molecular patterns into the blood and the subsequent amplification of systemic inflammation in sepsis. Local expression of the cytokine TNF has been shown to be involved in the loss of gut barrier function, and hence this local TNF can be considered as a factor that amplifies a local effect to a systemic scale. TNF is first expressed as a transmembrane protein, which is cleaved and released as the mature 17 kDa form by ADAM17. Several MMP members can cleave and release TNF169,172,173,174,175. The protection of MMP13-deficient mice in sepsis was specifically accompanied by reduced TNF release, and we identified several MMP13 cleavage sites in the pro-TNF protein169. These findings suggest that MMP13 that is expressed locally in the gut activates TNF in an ADAM17-independent manner, which leads to gut permeability176.
It is interesting to note that the three prominent MMPs that seem to have a central role in sepsis, according to studies using MMP-deficient mice and inhibitors, are the collagenases: MMP1, MMP7 and MMP13. This could be a coincidence, as the substrates of these MMPs are markedly different; however, the coincidence could also be due to the strong evolutionary relationship between these three MMPs177. The genes that encode MMP1, MMP8 and MMP13 are located in one cluster on proximal chromosome 9 in the mouse25. The three MMPs have diverse substrates but all target cells that are involved in sepsis, namely endothelium, choroid plexus and gut epithelium; therefore, a chemical inhibitor of all three MMPs might be a useful therapeutic to prevent the onset and progression of sepsis by inhibiting its progression at multiple stages. Agents that simultaneously inhibit MMP1, MMP8 and MMP13 do not exist yet, but MMP13 blockers with substantial MMP8 inhibitory potential have been described and could provide lead compounds to develop such triple inhibitors. Although a single inhibitor that can inhibit all of these targets might be difficult to develop, as their active sites and S1 and S1′ pockets differ substantially, combining MMP8- and MMP13-selective inhibitors could be promising in the treatment of sepsis.
Other MMPs have been recently shown to have a role in mouse models of sepsis. We reported that MMP7 deficiency is protective in endotoxaemia (owing to the reduction in α-defensin activation and the subsequent reduction in stimulation of IL-6 release by macrophages)178. It is important to note that the mechanism of enteric α-defensin activation in humans differs from that in mice and is MMP7-independent. This therefore excludes MMP7 as a potential therapeutic target to treat sepsis. MMP2 levels were increased in patients with sepsis and this was associated with decreased survival179. In addition, MMP2 inhibition reversed sepsis-induced BBB permeability and reduced brain inflammation and oxidative damage in an animal model of sepsis149. However, there are no reports showing whether MMP2 deficiency or inhibition is correlated with better overall outcome in mouse models of sepsis.
MMPs in intestinal inflammation. The functional integrity of the gut barrier is crucial for intestinal immune homeostasis. Damage to the epithelium triggers inflammatory responses owing to bacterial antigens that enter the lamina propria180. Proteolytic enzymes such as MMPs are secreted by both resident and infiltrating cell types and modulate the intestinal barrier function181. Consequently, MMPs are involved in the pathophysiology of several intestinal inflammatory disorders, including inflammatory bowel disease (IBD), necrotizing enterocolitis (NEC), collagenous colitis and diverticulitis182. Inhibitor and knockout studies indicate that some of these MMPs might have therapeutic potential (Fig. 4; Table 3).
IBD, which is an umbrella term that includes Crohn's disease and ulcerative colitis, results from both dysregulated genetic factors and environmental factors. A combination of commensal microbiota and aberrations in epithelial cells and the immune system contribute to IBD progression183. The use of 2,4,6-trinitrobenzenesulphonic acid (TNBS) or dextran sulphate sodium (DSS) to induce colitis in mice or rats are two valuable IBD models for gaining a better understanding of acute inflammatory processes in IBD.
Although TNF antagonists are often successfully used to treat IBD184, not all patients respond to these drugs and could therefore benefit from alternative treatments185, which might include MMP inhibitors. Indeed, data from both mice and human studies suggest that MMPs have a detrimental role in IBD. Although additional studies are needed, one study revealed that single nucleotide polymorphisms in MMP3, MMP8, MMP10 and MMP14 are significantly associated with an increased risk of developing ulcerative colitis186. Furthermore, treatment with the broad-spectrum MMP inhibitors batimastat or marimastat ameliorated the inflammatory alterations in TNBS-induced colitis in rats187,188. Similarly, AE-941, which is a natural inhibitor of MMPs that is derived from shark cartilage189,190, administered by gastric lavage in a rat model of ulcerative colitis, had therapeutic effects191. Also, minocycline (a semisynthetic tetracycline that inhibits MMPs) protected mice from DSS- and TNBS-induced colitis192, whereas ilomastat (a broad-spectrum MMP inhibitor) protected rats from TNBS-induced ulcerative colitis193. The orally active MMP inhibitor ONO-4817 (Table 1), which inhibits MMP2, MMP3, MMP8, MMP9, MMP12 and MMP13 but not MMP1 and MMP7, reduced DSS-induced inflammatory cell infiltration and mucosal cell disruption194. However, the synthetic MMP inhibitor CGS-27023-A did not influence mucosal repair in a rat model of DSS-induced colitis despite the significant decrease in extent and severity of epithelial injury195. Collectively, these studies support the hypothesis that MMP inhibition is an attractive and promising strategy for treating IBD and that these inhibitors have therapeutic potential. Selective targeting of the pathological MMPs is probably a more clinically appropriate approach to avoid the undesirable side effects that are associated with broad-spectrum MMP inhibition.
Only a few studies have addressed the role of single MMPs in the pathology of IBD. MMP13 gene expression was significantly increased in the colonic mucosa of patients affected by ulcerative colitis196. We have shown that the absence of MMP13 is slightly protective in a model of DSS-induced colitis, and we attributed this to MMP13-dependent cleavage of pro-TNF into bioactive TNF169. Epithelial-derived MMP9 is absent in normal colonic tissue but is upregulated in both the serum and tissue of patients with IBD, and this upregulation is associated with higher disease activity197,198,199.
Apart from the use of MMP9 as a biomarker for IBD, several animal studies revealed that MMP9 also drives colitis, making it an interesting therapeutic target for IBD200,201,202,203,204. Both prophylactic and therapeutic treatment of mice with antibodies that block MMP9 function substantially attenuated the severity of DSS-induced colitis105. By contrast, MMP2, another gelatinase that has structurally similar active sites and substrates to MMP9, protected against the development of colitis205. However, the absence of both MMP9 and MMP2 in colitis showed that MMP9-mediated tissue injury overrides the protective effect of MMP2 during colitis. This suggests that treatment of colitis by inhibiting MMP9 might be beneficial even if it also inhibits MMP2 (Ref. 206).
MMP8 also seems to have a role in IBD, as suggested by the increased MMP8 levels in patients with IBD and in mice with DSS-induced colitis199. Increased mucosal and plasma levels of MMP1 were correlated with the presence of ulcerative colitis in patients207,208,209. MMP1 promoted secretion of TNF in a positive feedback manner to cause further injury in the colon mucosa210. However, no studies are available on therapeutic MMP1 inhibition. Another MMP that is often suggested to have a detrimental role in IBD is MMP3. Plasma cells from patients with Crohn's disease and ulcerative colitis expressed significantly higher levels of MMP3 protein and transcripts than controls211, and this was also reflected in mucosal tissue and correlated with morphological damage212. Additionally, lamina propria myofibroblast-derived MMP3 activated neutrophil chemoattractant CXC-chemokine ligand 17 (CXCL7) and resulted in increased inflammation in the intestinal epithelium213. Interestingly, in vivo administration of MMP3-specific small interfering RNAs (siRNAs) significantly protected mice from DSS-induced colitis214.
Another MMP that has been associated with a protective role in IBD is MMP10. Studies in MMP10-deficient mice demonstrated that MMP10 seems to be required for resolution of DSS-induced colonic damage215. By contrast, MMP10 downregulation through intraperitoneal injection of MMP10-specific siRNAs did protect against colitis, as evidenced by a smaller reduction in body weight and a reduction in DSS-induced loss of crypts and epithelial layer destruction in treated mice compared with controls214. These contradictory results suggest that MMP10 mediates cell-dependent protective and detrimental roles in colitis.
Despite promising results in mouse models of colitis and data from human patients that link some MMPs (for example, MMP9 and MMP3) with disease severity, no clinical trial has studied the use of MMP inhibitors to treat IBD. First, more research is needed to study the therapeutic potential of MMPs in IBD, as not many MMPs have been studied in detail in this context. Moreover, the mouse models that are commonly used to elucidate MMP activity and to evaluate MMP inhibitors are often acute colitis models, whereas fibrosis, which is only present in chronic models, is more likely to be linked with exacerbated MMP activity. It is also important to note that several MMPs have a pivotal role in wound healing, which suggests that therapeutic MMP inhibition could have adverse effects.
NEC is the most common gastrointestinal disease to affect neonates and is associated with destruction of the intestinal barrier216. Local TNF concentrations are elevated in NEC and are thought to activate MMPs, which have a role in NEC-associated tissue remodelling and cell migration. MMP3 seemed to be strongly expressed in NEC, which could partly explain the pathophysiological inflammatory response at the onset of NEC217. Other MMPs were also upregulated in NEC samples: MMP7 was upregulated in the epithelium; MMP26 and MMP1 were upregulated in stromal cells; MMP12 was upregulated in both epithelial and stromal cells; and MMP9 was upregulated in inflammatory cells. By contrast, MMP19 was downregulated218.
Collagenous colitis is a rare inflammatory disease of the colon associated with chronic and watery diarrhoea. In the inflamed region, lymphocytes are present and the subepithelial collagen network is thickened. The excessive diarrhoea is linked to disturbed diffusion and absorption of water owing to thickening of the subepithelial layer. Increased MMP1 expression was observed at specific regions of the inflamed gut219.
Diverticulitis is a common digestive disease that involves the formation of pouches or diverticula within the bowel wall. Turnover of ECM plays a pivotal part in this disease. Indeed, mucosal samples from patients with diverticulitis showed increased expression of several MMPs, such as MMP1 and MMP3 (Refs 220,221).
Until now, despite the clear detrimental role of several MMPs in the pathophysiology of NEC, collagenous colitis and diverticulitis, no reports are available on the therapeutic potential of MMP inhibition in these inflammatory diseases. Therefore, further research is needed before therapeutic MMP inhibition can be an option for these gastrointestinal disorders.
MMPs in brain inflammation. The brain has long been thought to be an immunologically privileged organ owing to the BBB, which effectively prevents contact between the peripheral blood and the brain. Impermeability at the BBB is assured by tight junction protein complexes that closely connect the brain endothelial cells. MMPs have been implicated in a broad range of brain diseases, including stroke, traumatic brain injury, multiple sclerosis, hypoxic ischaemia, Alzheimer's disease, meningitis and spontaneous intracerebral haemorrhage222,223,224,225,226,227,228 (Table 4). By degrading the neurovascular matrix, MMPs promote injury of the BBB as well as oedema and haemorrhage.
The most extensively studied MMP in brain inflammation is MMP9, and its involvement in ischaemic stroke was recently reviewed229,230. Interestingly, MMP9 is increased in both cerebrospinal fluid and plasma of patients with a traumatic brain injury231, and peripheral blood MMP9 levels predict lesion volume in acute stroke232. Genetic knockout of Mmp9 protected the immature brain from BBB rupture and inflammation after hypoxia–ischaemia233 and protected from motor deficits in a model of traumatic brain injury234. Moreover, MMP9 deficiency diminished BBB leakage, infarct volume and inflammatory cell infiltration after cerebral ischaemia235,236. Similarly, MMP9 deficiency attenuated infarct size and behavioural abnormalities, and decreased neural cell adhesion molecule levels after middle cerebral artery occlusion in mice237. These observations were confirmed by successful therapeutic targeting of MMP9 via various methods including lentiviral-mediated Mmp9 gene silencing238, an MMP9-neutralizing monoclonal antibody239 and a liposomal formulation containing MMP9-specific siRNA240. Similarly, treatment with an MMP9 inhibitor prevented BBB breakdown in Wistar rats subjected to pneumococcal meningitis. Similar results were obtained with an MMP2 and a dual MMP2 and MMP9 inhibitor138.
Despite these promising results, it is important to realize that MMP9 and MMP2 are thought to improve repair or regeneration after nervous system injury via several mechanisms, such as cytoskeletal interactions, axonal outgrowth and guidance241. These positive effects of MMP9 and MMP2 again highlight the importance of understanding all of the functions of a particular MMP before considering therapeutic inhibition241. MMP2 deficiency had no effect on acute brain injury after focal ischaemia242. Deficiency of another MMP whose role in brain inflammation has not yet been defined, MMP3, only delayed inflammation and hippocampal neuronal death following global ischaemia243.
The potency of several synthetic, often broad-spectrum, MMP inhibitors has been studied in mouse and rat models of brain inflammation. SB-3CT, which is a competitive, mechanism-based, dual inhibitor of MMP2 and MMP9, effectively attenuated MMP9 activity, reduced brain lesion volumes and prevented neuronal loss and dendritic degeneration in an experimental mouse model of traumatic brain injury244. Similarly, SB-3CT attenuated behavioural impairments and hippocampal loss after traumatic brain injury in rats245. It also protected the neurovasculature from embolic focal cerebral ischaemia246, but it failed to confer significant neuroprotection after a hypoxic ischaemia insult247. Early brain injury following subarachnoid haemorrhage induction, reflected by neuronal cell death, was reduced in the presence of SB-3CT compared with controls248.
The broad-spectrum MMP inhibitor doxycycline reduced BBB permeability owing to reduced loss of collagen type IV249, attenuated recombinant tissue plasminogen activator (tPA)-induced oedema and haemorrhage250, and reduced neuronal cell death owing to reduced laminin degradation251. Treatment of stroke-prone spontaneously hypertensive rats with doxycycline reduced damage after transient cerebral ischaemia252. It was recently shown that the protective effects of doxycycline against BBB damage induced by reperfusion might be related to the upregulation of tight junction proteins and inhibition of MMP2, MMP9 and protein kinase Cδ253. Minocycline treatment reduced brain infarct volume, inflammation and neuronal death in brain ischaemia254,255. Minocycline in combination with aspirin protected from the consequences of cerebral ischaemia in animal models of diabetes by inhibiting MMP2 and MMP9 (Ref. 256). Doxycycline and minocycline are both broad-spectrum inhibitors of several proteins (including MMPs), and further studies with more specific inhibitors are needed to find which MMPs have therapeutic potential.
Batimastat reduced recombinant tPA-induced haemorrhage and mortality257, myelin-binding protein degradation258, inflammation and neuronal death243, but it impaired recovery from stroke259. Several studies described protection at the level of the BBB and/or the tight junctions following treatment with BB-1101 — a variant of the broad-spectrum MMP inhibitor batimastat with a smaller allyl α-substituent — in brain ischaemia models260,261,262,263. One study revealed that BB-1101 blocked intranuclear MMP activity, resulting in a positive effect on the oxidation of DNA via reduced poly(ADP-ribose) polymerase 1 (PARP1) and X-ray repair cross complementing group 1 (XRCC1) degradation264. However, impaired long-term recovery after stroke was observed in one study263. Such a delay was also observed with FN-439, a tetrapeptidyl hydroxamic acid, and was linked to a reduced level of bioavailable vascular endothelial growth factor259. Another synthetic MMP inhibitor that was evaluated for its ability to treat brain inflammation is GM6001. Similar to the effects observed with other MMP inhibitors, mice treated with GM6001 showed decreased inflammation-induced BBB permeability, neuronal cell death and infarct size, as well as decreased neuroblast migration265,266,267,268,269. This inhibitor also prevented the haemorrhagic complications and ameliorated the behavioural abnormalities induced by tPA270. Finally, a novel MMP-inhibitor (Ro 28-2653) that inhibits MT1-MMP (also known as MMP14), MT3-MMP (also known as MMP16), MMP2, MMP8 and MMP9 significantly reduced brain injury when administered in the first 2 days after focal cerebral ischaemia271.
Clearly, therapeutic MMP inhibition in acute brain injury and stroke has considerable potential based on available mouse and human data. However, the difficulty will again be to avoid adverse effects of MMP inhibition, especially during stages of recovery. Therefore, detailed analyses of both detrimental and beneficial roles of MMPs must be conducted and inhibition of antitarget MMPs involved in tissue regeneration should be avoided. From the available data, MMP9 inhibition looks to be the most promising; however, it should be noted that several MMPs were, until now, not studied in detail, mainly owing to the lack of suitable detection and inhibitory tools. In addition, it has to be taken into account that the inhibitors will have to reach the central nervous system (CNS) to be effective. Delivery of compounds into the CNS can be achieved by intrathecal administration. This enables the bypassing of the BBB and would have the advantage of avoiding systemic side effects of the MMP inhibitors. However, intrathecal drug delivery is an invasive procedure, and thus complications can arise. Several delivery systems have been developed that attempt to bypass the BBB272,273, but this is beyond the scope of this Review.
MMP activity is delicately balanced and disturbances can have dramatic effects. Consequently, upregulated MMP activity has an important and often detrimental role in several inflammatory disorders. This makes MMPs attractive therapeutic targets. However, several issues need to be considered before therapeutic MMP inhibitor strategies can be implemented. First, further analyses of the spatiotemporal expression and function of individual MMPs in health and disease must be carried out. Second, specific MMP inhibitors need to be developed to reduce off-target effects.
Despite limitations, such as the possible compensatory increases in other MMPs, the use of knockout mice and other mouse models is often useful to study the role of specific MMPs. Indeed, many single-MMP knockout mice have been generated, yielding a wealth of information on the role of many individual MMPs in particular diseases. Unfortunately, not much has been invested in generating conditional MMP-deficient mice, which might be due to the lack of developmental defects in full-body knockout mice, with the exception of MT1-MMP. Consequently, MT1-MMP conditional knockout mice were generated274. Previous research with conventional MMP knockout mice already enabled researchers to identify MMPs that are possible therapeutic targets and MMPs that are antitargets. Identifying therapeutic targets with minimal adverse effects is unlikely to be easy, as MMPs modify a broad range of signalling pathways and regulate the activity of whole families of cytokines by precise proteolytic processing. Based on the identified substrates, ten of 24 mouse MMPs were suggested to be drug antitargets as their beneficial actions should not be inhibited275.
Another important limitation to developing MMP inhibitors is that none of the available animal models reflect the complex human situation. This makes it extremely difficult to extrapolate the outcome of MMP inhibition in animal models to humans. For example, the pathophysiological mechanisms in patients with sepsis are highly individualized. As such, specific tools should be developed in the near future to define these differences and tailor therapeutic strategies accordingly. In addition, not all MMPs have the same expression pattern and substrate repertoire in mice and humans. The most striking example of this is MMP7. Its expression is necessary for intestinal α-defensin processing in mice but it is not detected in human Paneth cells178. In humans, trypsin was identified as the enzyme responsible for intestinal defensin processing276.
To fully understand the role of MMPs in health and disease, it is essential to develop better tools, such as probes for in vivo imaging and more specific antibodies, in order to assess MMP expression and activity during different disease phases12. Such tools should preferentially be developed for individual MMPs. Most research has focused on MMP2 and MMP9, not because they are the most important MMPs but owing to the lack of MMP-specific antibodies and the ease of MMP2 and MMP9 zymography277.
The currently available imaging probes are based on optical imaging, positron emission tomography, fluorescence resonance energy transfer, single photon emission computed tomography, magnetic resonance imaging278 and photoacoustic modalities279. Various MMP-activatable optical probes have recently been developed for in vivo MMP imaging, but the use of fluorescent, synthetic, low-molecular-mass MMP inhibitors has also been suggested278,280,281. These optical probes are valuable tools to study localization of MMP activity. However, the use of these tools is impeded by the limited availability of probes that are specifically cleaved only by clearly defined MMPs and by a paucity of inhibitors that are specific to individual MMPs. In vivo imaging of MMP activity would help to determine the key regulatory points for therapeutic intervention1,282,283.
Although the selective inhibition of single targets in early stages of disease might be desirable, more widespread targeting of MMPs might be necessary at intermediate stages, even at the cost of inducing side effects. Moreover, although broad-spectrum inhibition is not desirable owing to possible side effects, an important remaining question is whether single or multiple targets need to be inhibited in certain diseases. Indeed, a better understanding of the overlapping metalloproteinase expression patterns and their effects in health and disease will help to formulate efficacious metalloproteinase inhibitors as therapeutics for immune diseases21. To complicate matters, the function of MMPs is often context-dependent. For example, in colitis, MMPs are detrimental during the inflammatory phase of the disease but essential for subsequent wound healing284. Consequently, a greater understanding of the involvement of individual MMPs in specific inflammatory disorders is essential to further explore the possibilities of therapeutic MMP inhibition21.
Years ago, the MMP research community realized the urgent need for MMP inhibitors of greater specificity. Selectivity is a primary goal of the design of MMP inhibitors in order to improve efficacy and to avoid unwanted side effects. It was originally thought that the musculoskeletal pain observed in clinical trials of anticancer MMP inhibitors was caused by MMP1 inhibition, resulting in the development of MMP1-sparing inhibitors17,18. Subsequently, the non-MMP metalloproteinases, such as ADAM and ADAMTS family members, were shown to have a role in the development of musculoskeletal pain52 and this was taken into account in ensuing inhibitor development. However, there is still debate about which metalloproteinase is eventually responsible for musculoskeletal pain. AZM551248 treatment of dogs indicated that inhibition of MMP1, MMP2, MMP3 and MMP9 was a key early event in acute fibrosis-type adverse effects that are considered consistent with the clinical findings of musculoskeletal pain in patients285. More recently, MMP2, MMP3, MMP7, MMP8, MMP9, MMP11, MMP12, MMP20, MMP26 and MMP28 were recognized as antitargets because inhibition of their activity might result in clinically unwanted side effects and initiation or worsening of disease. Consequently, their essential and beneficial activities should not be inhibited275. However, this does not necessarily exclude those MMP as drug targets, but the associated risk/benefit ratio has to be taken into account, and this can be context-dependent. Also, several ADAM and ADAMTS family members are considered to be antitargets. For example, inhibition of ADAMTS13, which is a metalloproteinase responsible for cleaving large multimers of von Willebrand factor into smaller units, causes thrombotic thrombocytopaenic purpura and genetic dysfunction of ADAMTS13, which results in a rare form of thrombocytopaenic purpura, known as Upshaw–Schülman syndrome286.
It is difficult to generate specific MMP inhibitors because of the broad structural similarity of their active sites and the dynamic functional interconnectivity of MMPs with other proteases, their inhibitors and substrates287. Although the clinically relevant goal for MMP inhibitor specificity may be to achieve ~1,000-fold difference in the relative affinity between MMPs, many current inhibitors fall short of this goal60.
A third generation of MMP inhibitors is currently being evaluated that are designed to block only the target MMP and to spare the antitargets6,288. In addition, off-target effects can be avoided by attempting to achieve the optimum level of MMP activity for normal physiological processes. This again highlights the need to fully unravel the MMP contribution to tissue homeostasis and their dysregulation in different pathologies, but this requires the development of specific and sensitive quantitative assays to determine MMP activity. Cheminformatics-based methods (that is, the combination of computational modelling of the drug–protein interactions and methods such as X-ray crystallography) facilitate rational drug design. This approach has already resulted in the identification of different selective inhibitors; for example, MMP13-specific drugs289.
Antibody-based MMP inhibitors may offer the selectivity and potency that are required. Interestingly, rational design of antibody-based, function-blocking MMP inhibitors enables targeting of the extracatalytic domains, which are central to proteolytic and non-proteolytic enzyme functions287. This may create new therapies that control dysregulated MMP activity without causing severe side effects. Unfortunately, the use of antibodies may be limited by reduced patient convenience as they are administered through the parenteral, rather than oral, administration route. However, the use of these highly specific MMP inhibitors does enable further characterization of the involvement of specific MMPs in pathophysiological processes. Moreover, parenteral administration may not be a barrier for some diseases; for example, patients with septic shock are treated in intensive care units and already have infusion lines for drug delivery290.
In addition, to reduce the levels of MMP inhibitors in systemic circulation and the consequent toxicity, it would be interesting to focus on more local administration, which can be achieved by, for example, topical application or targeted delivery. Therefore, it will be essential to determine the exact location of detrimental MMP activity and to develop organ-specific or cell-type-specific delivery systems.
In recent years, MMP signalling cascades have become even more complex as it is increasingly clear that MMPs do not act exclusively outside the cell but can also degrade proteins in the cytoplasm, mitochondria and nucleus12. The roles of intracellular MMPs are poorly understood, although recent studies have unravelled some of their functions291. Several MMPs292, such as MMP2 (Refs 293,294,295), MMP3 (Ref. 296) and MMP12 (Ref. 297), have intracellular activity. Although inhibition of intracellular MMP activity is more difficult than inhibition of extracellular MMP activity, this could enable more precise targeting of specific cell types by using cell-type-specific markers. Small-domain antibodies, such as nanobodies, may be constructed as bispecific molecules to direct specific MMP-blockers to specific cell types298.
In conclusion, we believe that there is still hope for MMP inhibition as a therapeutic approach for the treatment of inflammatory disorders. However, the success of this approach requires a full understanding of the biological processes in each particular disease condition to identify the crucial MMP targets that have to be inhibited. In addition, further research is needed to develop potent and selective agents to avoid the side effects of non-selective MMP inhibitors.
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This work was supported by FWO Vlaanderen, Belgium and by the IAP initiative of Belgian Society Policy. The authors thank A. Bredan for editing the manuscript.
The authors declare no competing financial interests.
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Vandenbroucke, R., Libert, C. Is there new hope for therapeutic matrix metalloproteinase inhibition?. Nat Rev Drug Discov 13, 904–927 (2014). https://doi.org/10.1038/nrd4390
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