Abstract
Gastrointestinal tumors have become a worldwide health problem with high morbidity and poor clinical outcomes. Chemotherapy and surgery, the main treatment methods, are still far from meeting the treatment needs of patients, and targeted therapy is in urgent need of development. Recently, emerging evidence suggests that kelch-like (KLHL) proteins play essential roles in maintaining proteostasis and are involved in the progression of various cancers, functioning as adaptors in the E3 ligase complex and promoting the specific degradation of substrates. Therefore, KLHL proteins should be taken into consideration for targeted therapy strategy discovery. This review summarizes the current knowledge of KLHL proteins in gastrointestinal tumors and discusses the potential of KLHL proteins as potential drug targets and prognostic biomarkers.
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Introduction
Gastrointestinal tumors refer to those occurring in the digestive system, mainly including gastric, liver, colorectal, and pancreatic cancers, according to WHO classification [1]. Because of diagnostic difficulties and high morbidity, treating gastrointestinal tumors remains a difficult problem worldwide. Current treatments mainly include surgical resection and chemotherapy, but their therapeutic benefit implies we are far from an efficient cure [2]. Targeted drugs should achieve better therapeutic effects, but few of them are applied for the treatment of gastrointestinal tumors, highlighting the urgent need for the development of novel drug targets and prognostic biomarkers.
Kelch-like (KLHL) proteins, encoded by Kelch-like (KLHL) gene family members, function as substrate adaptors of the Cul3-scaffold E3 ligase complex and are the key factors that recognize and interact with substrates. KLHL proteins (KLHLs) mediate the ubiquitination of substrates and determine degradation fate and are thereby responsible for maintaining substrate homeostasis. Since substrate homeostasis plays an essential role in a wide range of cellular life activities, the function of KLHLs as key regulators of protein homeostasis under physiological and pathological conditions should be emphasized.
In recent years, an increasing number of studies have revealed that KLHLs are recurrently dysfunctional in gastrointestinal tumors, which is associated with tumor progression, suggesting that aberrant KLHLs generate an imbalance in protein homeostasis. For example, studies revealed that decreased expression of Keap1 (KLHL19) promoted the growth of pancreatic cancer cells [3], and increased KLHL21 expression was closely related to unfavorable outcomes in patients with cholangiocarcinoma [4]. Based on the specificity and importance of KLHLs in regulating substrate ubiquitination and stability, targeted inhibition of KLHL function may provide new insights for gastrointestinal tumor therapy. Therefore, this review will provide an overview of the biological functions and clinical significance of KLHLs in gastrointestinal tumors, attempt to match different KLHLs to drug targets or prognostic biomarkers, and ultimately propose potential targeted strategies for gastrointestinal tumor therapy.
KLHL aberrations in gastrointestinal tumors and their clinical significance
Various aberrations of KLHLs are frequently found in many gastrointestinal tumors, including mutations, deletions, hypermethylation, fusions and aberrant expression (Table 1). These aberrations result in global proteome alterations and proteostasis imbalance, suggesting that KLHLs play crucial roles in gastrointestinal tumors. Several mutations in KLHL19 have been reported in gastrointestinal tumors, e.g., N222S in pancreatic cancer; F280L, Q82H, and G350S in gastric cancer; and Q359X in colorectal cancer [5, 6]. Many of these mutations cause constitutive activation of Nrf2, which is commonly associated with poor prognosis of patients. Surprisingly, mutations at the same site have been observed in various malignancies. For example, G379D has been found in liver and gallbladder cancers [7, 8]. Gene mutations commonly lead to a considerable loss of KLHL activities, followed by dysregulation of downstream proteins and disease development. Additionally, deletions and promoter hypermethylation have been discovered in gastrointestinal tumors. Full-length deletion of KLHL9 was observed in 5.46% of gastric cancers and might partly account for gastric tumorigenesis [9]. Hypermethylation, a vital epigenetic modification, was found in KLHL19 and KLHL35 in colorectal and liver cancers, respectively [10, 11]. Notably, low expression of these KLHLs induced by epigenetic alterations is associated with poor survival. Furthermore, fusion is another common cause of aberrations. The PHOSPHO2-KLHL23 fusion has been reported in both liver and gastric cancers [12, 13], and NR5A2-KLHL29 was detected in colorectal cancer [14]. Clinically, fusions display a tumor-specific pattern and are associated with prognosis.
Aberrant expression is the most typical type of aberration. For instance, it was reported that KLHL21 was highly expressed in hepatocellular carcinoma [15], whereas KLHL19, KLHL23, and KLHL30 had decreased expression [12, 16, 17]. KLHL4 and KLHL22 were downregulated in colorectal cancer [18, 19], while KLHL37 was upregulated [20]. In addition, we noticed that some KLHLs were important by data analysis, which drew little attention before [21]. For example, the expression levels of KLHL7 and KLHL15 were found to be elevated in esophageal cancer, while the levels of KLHL17 and KLHL36 were decreased in gastric cancer. Various KLHLs, such as KLHL5 and KLHL27, are typically highly expressed in gastrointestinal tumors. Based on their distinct expression profiles, the clinical significance of KLHLs needs to be determined. Reduced KLHL19 expression is related to poor overall survival in liver cancer [16]. A study revealed that higher KLHL21 expression was linked to unfavorable outcomes in cholangiocarcinoma [4]. Downregulation of KLHL39 in colorectal cancer was correlated with higher TNM stage and shorter survival [22]. Additionally, we assessed the expression of the abovementioned KLHLs that had previously garnered little interest in relevant samples. For example, increased expression of KLHL15 was associated with unsatisfactory survival in esophageal cancer, while there was a significant correlation between high KLHL36 expression and good outcomes in pancreatic cancer and cholangiocarcinoma.
KLHLs show distinct clinical significance and characteristic aberrant expression patterns, emphasizing the importance of KLHLs in gastrointestinal tumors. Some aberrations are tightly linked with gastrointestinal tumors, and such aberrations lead to sharply decreased tumor suppression or substantially increased tumor promotion. Decreased tumor suppression may suggest utility as a prognostic biomarker, and increased tumor promotion may suggest utility as a drug target. As adaptors, KLHLs participate in a range of biological processes due to their interactions with various substrates. Aberrations of KLHLs caused by pathological situations lead to substrate dysfunction, eventually resulting in malignant transformation and tumorigenesis. Here, we focus on several representative KLHLs and discuss their regulation of substrates.
The substrates and pathological dysfunction of KLHLs in gastrointestinal tumors
KLHLs are adaptors that interact with a variety of substrates in the E3 enzyme, consisting of three characteristic domains: the bric-a-brac, tramtrack, broad complex (BTB)/poxvirus and zinc finger (POZ) domain, the BACK domain, and the Kelch domain (Fig. 1). The Kelch domain specifically recognizes and interacts with substrates, and the BTB/POZ domain is responsible for binding the scaffold protein Cullin3. Subsequently, neddylated Cullin3 recruits the E2 enzyme and finally promotes the transfer of ubiquitin molecules from E2 onto substrates. Additionally, the BACK domain is a conserved and poorly described region, and some mutations in this domain are reported to be linked to gastrointestinal tumors, e.g., gastric cancer, liver cancer, and cholangiocarcinoma [6, 8].
a Schematic representation of KLHLs structure. KLHLs consist of BTB/POZ domain, BACK domain and Kelch domain. The BTB/POZ domain is essential for dimerization and contributes to CUL3 interaction. The Kelch domain is comprised of six identical motif repeats and mediates specific substrates recruitment. The BACK domain is served as a linker connecting two domains. b The biological process involved in KLHLs regulation. The KLHLs and CUL3 are both dimerized and form CUL3-KLHL complex to identify substrates. The complex then recruits the E2 enzyme when bound to RBX1 and NEDD8, and jointly transfers ubiquitin onto substrates for subsequent proteasome-mediated degradation.
It is well known that KLHLs perform cellular functions mostly by ubiquitination, during which they specifically interact with substrates. The properties of these substrates bestow distinct roles on KLHLs. If the substrate acts as an oncoprotein, the KLHL will correspondingly play vital anticancer roles. In contrast, if the substrate contributes to tumor suppression, the KLHL will possess pro-cancer functions. Research has identified bona fide substrates of a few KLHLs, while potential substrates that have been documented in the protein interactome as interacting with KLHLs have also been defined, but for such substrates, there is no experimental evidence. Thus, a summary of the substrates and pathological dysfunction of KLHLs in gastrointestinal tumors is imperative to increase the understanding of KLHLs. Here, we provide a review of representative KLHLs (i.e., KLHL7, KLHL15, KLHL19, KLHL22, KLHL23, KLHL27, and KLHL36) and their substrates in gastrointestinal tumors (Fig. 2 and Table 2).
All listed KLHLs are high-expressed in tumor tissues compared to normal tissues. In tumor tissues, KLHLs whose high expression is correlated to low overall survival may match some properties of drug targets. Meanwhile, KLHLs whose high expression is correlated to high overall survival accordingly possibly fulfill some requirements of prognostic biomarkers. KLHLs in red match some properties of drug targets. KLHLs in green match some properties of prognostic biomarkers. CHOL cholangiocarcinoma, ESCA esophageal carcinoma, LIHC liver hepatocellular carcinoma, PAAD pancreatic adenocarcinoma, STAD stomach adenocarcinoma.
KLHL19
KLHL19, also known as Keap1, is the most thoroughly studied among the KLHL family members. It interacts with its typical substrate, Nrf2, forming the KLHL19-Nrf2 pathway to react against oxidative stress. To date, many proteins have been identified as substrates, and we focused on some representative proteins, namely, Nrf2, p62, and IKBKB.
Nrf2, named nuclear factor erythroid 2-related factor, is a key substrate of KLHL19. Normally, KLHL19 transmits ubiquitin to Nrf2 for degradation. Upon exposure to reactive oxygen species (ROS), KLHL19 is inhibited by conformational changes, thereby stabilizing Nrf2 and eventually leading to downstream antioxidant gene activation. Nrf2 is presumably an oncoprotein that is constitutively and widely activated for protection in gastrointestinal tumors. In a mutant K-ras/p53 mouse model, KLHL19 deletion accelerated cholangiocarcinoma formation alongside Nrf2 activation [23]. Enhanced KLHL19-mediated ubiquitination of Nrf2 triggered ROS-induced cell death in gastric cancer [24]. Knockdown of Nrf2 led to sorafenib-induced ferroptotic events, while KLHL19 knockdown contributed to ferroptosis resistance in liver cancer cells [25]. In addition, some Nrf2 mutations were reported to lead to aberrant regulation of the KLHL19-Nrf2 pathway to protect cancer cells [26].
p62, also called SQSTM1, has emerged as a multifunctional signal hub. p62 interacts with KLHL19 via competitive binding, causing Nrf2 activation [27]. Autophagy is another essential process impacted by p62. In a xenograft mouse model, KLHL19 displayed a higher affinity for phosphorylated p62 for subsequent autophagy-mediated degradation, which significantly facilitated liver tumor growth [28]. KLHL19 accumulation along with p62 reduction generated an inflammatory and senescent phenotype, thereby promoting cancer development in an orthotopic pancreatic cancer model [29].
IKBKB is another recognized substrate. KLHL19 facilitated IKBKB ubiquitination to act as a tumor suppressor while IKBKB deficiency accordingly impeded inflammation-induced intestinal carcinogenesis in a mouse model [30, 31]. Consistently, the pro-cancer ability of IKBKB was demonstrated in a gastric cancer model [32]. Additionally, research revealed that increased KLHL19 and decreased IKBKB contributed to the improvement of hepatic steatosis, whereas IKBKB facilitated lipogenesis and hepatocellular carcinogenesis in vivo [33, 34].
KLHL15
KLHL15 was first identified in silico, and its mRNA is universally expressed in diverse tissues. KLHL15 is reported to be related to agenesis of the corpus callosum [35]. Nevertheless, more studies of KLHL15 to determine its biological mechanisms are underway. Based on the published literature, CtIP, PPP2R5B, DCX, DCLK1, and DCLK2 have all been identified as substrates of KLHL15.
CtIP, also known as RBBP8, functions in genome maintenance, especially in DNA double-strand break repair. Due to its unique function, CtIP is commonly dysregulated in gastrointestinal tumors. For example, CtIP was upregulated in HBV-related liver cancer cells [36]. Knockdown of CtIP slowed the gastric cancer cell growth rate, while inhibition of its ubiquitination by KLHL15 led to chemoresistance and cancer development [37, 38]. Additionally, depletion of CtIP decreased metastasis in an orthotopic colon cancer model [39]. PPP2R5B is a regulatory subunit of PP2A, but its role in gastrointestinal tumors remains unknown. DCX, DCLK1, and DCLK2 were found to be bona fide substrates in a study of neuronal dendritogenesis [40]. DCX and DCLK2 are both rarely studied in gastrointestinal tumors. In contrast, increased expression of DCLK1 has been universally detected in numerous gastrointestinal tumors, e.g., esophageal, colon, and gastric cancers, while its ubiquitination regulator, KLHL15, is expressed at low levels in gastrointestinal tumors [41,42,43]. A DCLK1-selective inhibitor exhibited significant antitumor effects against cholangiocarcinoma cells in vitro [44]. Recently, numerous studies have illustrated the relationship between DCLK1 and stemness. DCLK1 is recognized as a marker of cancer stem cells in many gastrointestinal tumors [45, 46]. For example, in one study, when injuries and inflammation occurred, DCLK1-positive cells acquired carcinogenic abilities, inducing oncogenic transformation in the pancreas [47].
KLHL22
KLHL22 plays significant roles in tumorigenesis, mitosis, and immune homeostasis. One study revealed that KLHL22 was downregulated in colorectal cancer and attenuated cell invasion, migration, and proliferation in vitro [19]. It has been reported that DEPDC5, PLK1, and PD-1 are substrates of KLHL22, while ADRA1A and NANOG are potential substrates.
DEPDC5, a crucial and conserved subunit of GATOR1, undergoes ubiquitin linkage mediated by KLHL22. It has been reported that DEPDC5 deficiency promotes the growth of gastrointestinal stromal tumor xenografts in nude mice, while its stabilization resulting from KLHL22 depletion hinders tumor progression [48, 49]. Moreover, knockdown of DEPDC5 potentiated ROS resistance in liver cancer, which was associated with poor outcomes [50]. PLK1, a regulator of mitosis, is regulated in localization instead of protein stability [51]. A selective inhibitor of PLK1 had anticancer effects in esophageal cancer both in vivo and in vitro [52]. Overexpression of PLK1 hindered liver cell death, while knockdown reversed this effect [53]. Furthermore, PD-1 is a novel substrate of KLHL22 and prevents excessive inhibition of T cells [54]. PD-1 is normally expressed on the surface of T cells, and inhibition of PD-1 to upregulate the T-cell response and improve the microenvironment is viewed as a promising strategy for cancer therapy. Furthermore, several inhibitors targeting PD-1, such as nivolumab and pembrolizumab, are approved for the treatment of some gastrointestinal tumors and display good efficacy [55].
ADRA1A is a G protein-coupled receptor that senses catecholamines. NANOG is considered a biomarker of cancer stem cells that regulates self-renewal and maintains stemness. In colorectal cancer tumor-bearing mice, NANOG knockdown led to a significant decrease in the tumor growth [56]. Similarly, degradation of NANOG weakened the pancreatic cancer phenotype in vitro [57].
KLHL23
KLHL23 is an actin-binding protein. A study demonstrated that KLHL23 hindered the epithelial-mesenchymal transition of liver cancer cells by impeding actin cytoskeleton remodeling [12]. According to the study, actin was found to be the only definite substrate, while the other 5 proteins, namely, ANXA1, ANXA7, BNIP3L, CDKN1A, and TK1, were identified as potential substrates.
ANXA1 and ANXA7 both belong to the annexin superfamily and can promote or suppress gastrointestinal tumors [58, 59]. BNIP3L, also known as NIX, profoundly impacts mitophagy. In a xenograft model, BNIP3L-dependent mitophagy upregulated glycolysis, thereby promoting the cancer stemness phenotype of liver cancer cells [60]. In addition, BNIP3L deficiency markedly retarded tumor development and augmented survival in a pancreatic cancer mouse model [61]. CDKN1A, famously known as p21, is described as an essential regulator of the cell cycle and DNA damage repair. CDKN1A plays dual roles in cancer depending on cell type [62]. Increased expression of CDKN1A impeded colorectal tumor growth [63]. CDKN1A inhibition was reported to promote cancer progression in a gastric cancer mouse model [64]. However, CDKN1A sustained regeneration in liver injury and promoted hepatocarcinogenesis in vivo and in vitro [65]. Research on TK1 in gastrointestinal tumors has rarely been conducted.
KLHL27
KLHL27 was first characterized as a human homolog of mouse intracisternal a particle-promoted placenta. Moreover, KLHL27 is highly expressed in breast cancer [66]. The literature shows that KLHL27 has no substrate except actin, but it has 2 potential substrates, namely, Hook2 and Lig4.
Hook2 is essential for mitosis and cytokinesis. Given its increased serum levels, Hook2 hypothetically encodes a tumor antigen and is regarded as a potential diagnostic biomarker for esophageal, gastric, and colon cancers [67]. Lig4 is a DNA ligase that is indispensable in the nonhomologous end-joining repair pathway. Consistently, Lig4 knockdown decreased radioresistance in colorectal cancer cells [68].
KLHL36
KLHL36 has rarely been described to date. It has been reported that KLHL36 expression can be elevated by TNFα [69]. Based on the literature, Trim55, and Trim63, also known as Murf2 and Murf1, respectively, are potential substrates.
Trim55 and Trim63 can function as E3 ligases. High expression of Trim55 hampered the migration and invasion of liver cancer cells in vitro [70]. Trim63 is involved in cancer cachexia, but gastrointestinal-related research is limited.
KLHL7
KLHL7 is mostly reported to be associated with genetic diseases. TUT1, also known as Star-PAP, has been identified as the only known substrate to date implicated in U6 snRNA maturation. Fbxl17 has been identified as a potential substrate that sustains cancer cell proliferation by ubiquitination. However, the impacts of these proteins on gastrointestinal tumors remain unexplored.
In summary, accumulating experimental evidence has established that KLHLs promote or suppress gastrointestinal tumors in a substrate-dependent manner. If a substrate is a protumor factor, the KLHL suppresses tumor development by promoting substrate degradation and therefore could match properties of a biomarker of good prognosis. On the other hand, if a substrate is a tumor suppressor, the KLHL will restrain the antitumor functions of the substrate and promote tumor growth, suggesting that the KLHL might conform to the characteristics of a drug target. Therefore, based on the existing reports and database results, KLHL7, KLHL15, KLHL23, and KLHL27 could be potential candidates of drug targets, whereas KLHL19, KLHL22, and KLHL36 meet certain criteria of prognostic biomarkers.
Strategies to target KLHLs for gastrointestinal tumor therapeutics
Targeted therapies are emerging for gastrointestinal tumors and have shown tangible benefits with fewer side effects and higher efficacy than chemotherapy and radiotherapy. Targeting KLHLs is regarded as a feasible and promising approach due to their crucial roles in gastrointestinal tumors. As adaptors of E3 enzymes, KLHLs are involved in multiple cellular activities at key points, and their dysfunction often leads to tumorigenesis. Furthermore, KLHL inhibition strategies must consider the specificity of individual KLHLs. Due to the high expression of certain KLHLs in gastrointestinal tumors and the specificity of interactions between KLHLs and substrates, targeting KLHLs will not impair intracellular biological processes in normal tissues. Instead, inhibitors can be concentrated in tumor cells and specifically repress them, tremendously minimizing unfavorable side effects. More importantly, KLHLs are targetable, and several strategies are proposed here.
Protein‒protein interaction (PPI) inhibitors, whether small molecules or peptides, have been designed to hinder interactions by binding to KLHLs. Different KLHLs possess unique Kelch domains that interact with specific substrates, offering a structural basis for designing PPI inhibitors with specificity that disrupts the KLHL-substrate interaction. To date, many studies have reported small molecule inhibitors. The K67 derivative 5d possessed potent inhibitory activity and attenuated chemoresistance in liver cancer, as demonstrated by cell experiments [71]. Another PPI inhibitor, esculetin, hindered proliferation and induced apoptosis of pancreatic cancer cells in vitro [72]. Furthermore, peptide inhibitors, such as cyclic peptide 3, are continually emerging [73]. Apart from traditional druggable sites, novel sites are constantly being uncovered to accelerate drug discovery. A study showed that dimethyl fumarate (DMF) bound to the top region of the KLHL19 Kelch domain instead of the bottom region, to which Nrf2 bound [74], facilitating the development of new potent selective drugs. Targeting the CUL3-KLHL interface is also a theoretical strategy. According to one study, disruption of the interaction between a hydrophobic groove of KLHL11 and the CUL3 N-terminal extension led to sharply decreased affinity [75], suggesting a promising target for KLHL11 inhibition. A designed stapled peptide was also reported to efficiently mimic the CUL3-BTB interaction [76], providing the possibilities for the subsequent development of inhibitors to disrupt the CUL3-KLHL interaction.
Allosteric inhibitors are commonly defined as inhibitors that bind to nonactive sites of enzymes, subsequently triggering conformational changes and ultimately altering enzyme activities. Taking KLHL19 as an example, Cys151, Cys273, and Cys288 are the major sensor residues among its 27 cysteines, which all sense ROS and electrophilic chemicals [77]. In the presence of oxidative stress, the conformation of KLHL19 changes as a consequence of modification, subsequently preventing Nrf2 degradation. Inhibitors of cysteines are mainly electrophiles that inactivate KLHL19, and one of them, DMF, has been approved for the treatment of relapsing multiple sclerosis. Furthermore, the potency of some inhibitors has been confirmed to impede gastrointestinal tumor growth. TCE 31 reduced the formation of preneoplastic foci in the livers of aflatoxin B1-treated mice [78]. Moreover, sulforaphane triggered apoptosis of colon cancer cells by G2/M phase arrest in vitro [79].
Promoting KLHL degradation appears to be a direct and effective method to hamper KLHL functions. To date, proteolysis-targeting chimeras (PROTACs) have been developed as a main tool to target proteins of interest (POIs) for degradation by hijacking the ubiquitination system. A PROTAC is composed of three parts. One ligand binds to the POI, another binds to the E3 ligase, and a linker connects the ligands in the middle. PROTACs should be designed to target unique regions of KLHLs that enable formation of distinct structures and binding pockets, ensuring specific binding with KLHLs. A study reported that a PROTAC targeting KLHL19 successfully triggered the degradation of Tau [80], suggesting that KLHLs could be targeted by PROTACs; this result indicated that PROTACs could be designed to inactivate KLHLs by degradation if one ligand was targeted for KLHLs and another ligand recruited an E3 ligase. A number of PROTACs have shown strong effects in gastrointestinal tumors [81]. In addition, research found that in Drosophila, KLHL19 and KLHL18 could be self-degraded by ubiquitination in a proteasome-independent manner [82]. Although the detailed mechanism of KLHL self-ubiquitination is unclear, it offers potential novel insights into targeting KLHLs for degradation, which could ultimately be translated into new drugs.
Discussion
In this review, literature searches and sample analyses were performed to identify KLHL aberrations in gastrointestinal tumors and their clinical value. Then, based on their significance, we focused on several representative KLHLs, i.e., KLHL7, KLHL15, KLHL19, KLHL22, KLHL23, KLHL27, and KLHL36, and provided a systematic summary of their substrates and pathological dysfunction in gastrointestinal tumors to provide novel insights. Furthermore, possible therapeutic strategies to inhibit aberrant KLHLs were proposed. Our review highlights a number of intracellular roles of KLHLs in gastrointestinal tumors and thereby provides a theoretical basis for KLHL inhibitor design.
Gastrointestinal tumors are highly heterogeneous. Even if the clinical and pathologic features are similar, the eventual outcomes are different. Thus, biomarkers of gastrointestinal tumors are of vital importance and urgently needed. Many studies have revealed that some KLHLs are related to prognosis in gastrointestinal tumors. Moreover, the majority of KLHLs are located in the cytoplasm and thereby can be easily detected. However, many KLHLs are analyzed based on immunohistochemistry, which cannot be easily performed in the clinic. The accuracy, sensitivity, robustness, etc., of such assays must all be determined and verified. This review provides potential biomarkers for the diagnosis of gastrointestinal tumors.
KLHLs are potential ideal therapeutic targets for treating gastrointestinal tumors for the following reasons: (1) The first is the effectiveness of intervention targets (KLHLs), and studies have revealed that biological methods, such as knockdown, of KLHLs has a therapeutic effect in gastrointestinal tumors. (2) The second is the targetability of KLHLs. At present, PPI inhibitors, allosteric inhibitors and PROTACs are all technically well developed, and substantial evidence shows that some inhibitors derived from the above strategies show inhibitory effects on KLHLs. (3) The third reason concerns specificity. The specificity of the KLHL protein structure (the unique substrate binding pocket) and the specificity of inhibitor targeting strategies (PPIs and PROTACs) both ensure the specificity of the targeted inhibition of KLHLs. Apart from inhibitors of KLHLs with tumor-promoting function, activators of tumor suppressor KLHLs are another promising option. However, activators that can rescue KLHL functions have not been studied in gastrointestinal tumors, and their technical feasibility remains to be further evaluated and demonstrated. Furthermore, current knowledge about KLHLs in gastrointestinal tumors is still limited. For example, not all of the substrate proteins mentioned in this review fit the characteristics of definite ubiquitinated substrates of KLHLs, and to expand the list of substrates, several interacting proteins were defined as potential substrates though sufficient experimental evidence is lacking. Therefore, further research should focus on substrate identification and biological function clarification. Only significant progress in target validation can facilitate the development of KLHL inhibitors. Furthermore, inhibitor development still faces some challenges: (1) the moderate efficacy of PPI inhibitors should be improved, (2) some allosteric inhibitors of KLHLs will need to be identified without knowledge of the allosteric site, and (3) the good druggability of PROTAC molecules should be ensured on the premise of ensuring effectiveness.
In conclusion, we described KLHL aberrations and their practical significance in gastrointestinal tumors, outlined the biological functions of representative KLHLs and their substrates under pathological conditions in gastrointestinal tumors, and finally offered feasible strategies for therapies. KLHLs are important in cells because of their extraordinary abilities. KLHLs have substrate-dependent antitumor and protumor effects in practice. KLHL7, KLHL15, KLHL23, and KLHL27 could be potential candidates of drug targets. The availability of many inhibitors makes it possible to develop drugs targeting KLHLs in gastrointestinal tumors. In addition, KLHL19, KLHL22, and KLHL36 could be potential targets for the identification of prognostic biomarkers in gastrointestinal tumors. This review provides guidelines for a comprehensive understanding of the biological functions of KLHLs and offers references for the feasible development of inhibitors targeting KLHLs in gastrointestinal tumors.
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This work was supported by the State Key Program of the National Natural Science Foundation of China (No. 81830107) and the Fundamental Research Funds for the Central Universities (No. 2021XZZX037).
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Fu, Ab., Xiang, Sf., He, Qj. et al. Kelch-like proteins in the gastrointestinal tumors. Acta Pharmacol Sin 44, 931–939 (2023). https://doi.org/10.1038/s41401-022-01007-0
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DOI: https://doi.org/10.1038/s41401-022-01007-0
