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Molecular targets of aspirin and cancer prevention

British Journal of Cancer volume 111, pages 6167 (01 July 2014) | Download Citation

This article has been updated


Salicylates from plant sources have been used for centuries by different cultures to treat a variety of ailments such as inflammation, fever and pain. A chemical derivative of salicylic acid, aspirin, was synthesised and mass produced by the end of the 19th century and is one of the most widely used drugs in the world. Its cardioprotective properties are well established; however, recent evidence shows that it can also act as a chemopreventive agent. Its antithrombotic and anti-inflammatory actions occur through the inhibition of cyclooxygenases. The precise mechanisms leading to its anticancer effects are not clearly established, although multiple mechanisms affecting enzyme activity, transcription factors, cellular signalling and mitochondrial functions have been proposed. This review presents a brief account of the major COX-dependent and independent pathways described in connection with aspirin’s anticancer effects. Aspirin’s unique ability to acetylate biomolecules besides COX has not been thoroughly investigated nor have all the targets of its primary metabolite, salicylic acid been identified. Recent reports on the ability of aspirin to acetylate multiple cellular proteins warrant a comprehensive study to investigate the role of this posttranslational modification in its anticancer effects. In this review, we also raise the intriguing possibility that aspirin may interact and acetylate cellular molecules such as RNA, and metabolites such as CoA, leading to a change in their function. Research in this area will provide a greater understanding of the mechanisms of action of this drug.


The common household drug, aspirin (acetylsalicylic acid) has been around for more than a century. Its basic mechanism of action as an anti-inflammatory agent is well documented, yet newer beneficial effects and modes of action keep on adding to its ever-expanding therapeutic repertoire. It is currently used extensively as a cardioprotective and antithrombotic agent. In recent years, aspirin has generated significant interest as a potential chemopreventive agent supported by strong evidence from epidemiological data. Numerous clinical observations and laboratory studies have shown that regular use of aspirin is associated with a reduced risk for colorectal, oesophageal, breast, lung, prostate, liver and skin cancers (Harris et al, 2005; Kaiser, 2012; Sahasrabuddhe et al, 2012; Gamba et al, 2013; Veitonmaki et al, 2013). Aspirin appears to have both chemopreventive and chemotherapeutic effects (Chan et al, 2009; Holmes et al, 2010; Bastiaannet et al, 2012; Rothwell et al, 2012); however, aspirin is not currently prescribed for cancer prophylaxis owing to its adverse effects such as the risk of bleeding. Depending on the conditions being treated, aspirin is used at a range of doses from 75 mg (antiplatelet) to 325–600 mg (analgesic) to 1.2 g (anti-inflammatory) (Dovizio et al, 2013). Following oral administration, low-dose aspirin gives a peak plasma concentration of 7 μM; however, analgesic and anti-inflammatory doses can yield plasma concentrations ranging from 30 to 150 μM (Dovizio et al, 2013). These represent plasma concentrations of intact acetylsalicylic acid. The primary metabolite of aspirin is salicylic acid. The plasma salicylate concentrations obtained from the hydrolysis of low-dose aspirin is estimated to be 15 μM, whereas the analgesic and anti-inflammatory doses can yield concentrations ranging from 500 to 2500 μM (Dovizio et al, 2013). Incidentally, most of aspirin’s anticancer effects have come to light during the course of its use as a cardiovascular prophylactic and/or analgesic agent. Studies have shown that doses ranging from 81 to 325 mg taken over prolonged periods of time, decrease the incidence and mortality associated with colorectal cancer (Rothwell et al, 2010, 2012; Dovizio et al, 2013). Several studies using colon cancer cells and tumour models have demonstrated that aspirin can prevent cancer cell growth and induce apoptosis. Various mechanisms and cellular pathways have been identified as contributors to these effects (Thun et al, 2012; Dovizio et al, 2013).

Proposed mechanisms of action

Aspirin’s molecular mechanism of action was discovered in the 1970s when it was demonstrated that it irreversibly acetylates and inactivates the cyclooxygenase enzyme (prostaglandin H-synthase) (Vane, 1971; Roth et al, 1975). The COX enzymes are involved in the synthesis of cyclic endoperoxides from arachidonic acid (AA) forming prostaglandins, prostacyclins and thromboxanes, which have a wide array of effects. Aspirin is unique because it is the only non-steroidal anti-inflammatory drug (NSAID) that irreversibly inactivates both isoforms of the COX enzymes (COX-1 and COX-2), which bring about its anti-inflammatory, antipyretic and analgesic effects. Although the precise mechanisms by which aspirin exerts its anticancer effects are yet to be elucidated, both COX-dependent and independent mechanisms have been proposed (Thun et al, 2012).

Cox-dependent mechanisms

Aspirin has been shown experimentally to induce apoptosis (Shiff et al, 1996, 2003; Gupta and DuBois, 1998; Moyad, 2001; Rao and Reddy, 2004) and to inhibit angiogenesis (Sawaoka et al, 1999; Abdelrahim and Safe, 2005) in cancer cells. Most hypotheses have focused on aspirin’s ability to affect AA metabolism by permanently inactivating the ‘housekeeping’ COX-1 and the ‘inducible’ COX-2 enzymes by acetylating strategically located serine residues (Ferrandez et al, 2012).

Several COX-dependent pathways/downstream targets have been identified in aspirin’s anticancer effects. Aspirin and its primary metabolite, salicylate has been shown to affect COX-2 expression at both transcriptional and posttranscriptional levels (Xu et al, 1999). One of the earlier reports demonstrated that aspirin and sodium salicylate decrease the synthesis of proinflammatory prostaglandins by reducing the transcription of COX-2 gene (Xu et al, 1999). Cyclooxygenase enzyme inhibition increases AA levels, which can prompt the conversion of sphingomyelin to ceramide, which is a well-known mediator of apoptosis (Chan et al, 1998). Aspirin is known to affect platelet function through COX inhibition. Cancer patients exhibit an increase in platelet activation that has been known to have a role in cancer progression and metastasis (Gay and Felding-Habermann, 2011). With its short plasma half-life of around 15–20 min, aspirin is much more effective at inhibiting COX-1 in anucleate platelets as opposed to inhibiting COX-2 in monocytes, thus causing a long-lasting defect in TXA2-dependent platelet function (Ferrandez et al, 2012). COX-2 is less sensitive to aspirin because inhibition of the inducible COX-2 requires higher doses of aspirin and shorter dosing intervals as nucleated cells can promptly resynthesise the enzyme. Cyclooxygenase-2 is known to be overexpressed in colon cancer (Eberhart et al, 1994; Williams et al, 1997), and some researchers postulated that activated platelets could bring about this overexpression in colorectal cancers via the production of IL-1β, PGDF and TGF-β (Sciulli et al, 2005).

Whereas COX-1 acetylation by aspirin abolishes its enzymatic activity, COX-2 acetylation modifies the enzyme in such a way that it performs an incomplete reaction ultimately resulting in the generation of lipoxins (Claria and Serhan, 1995), which inhibit cancer cell proliferation and angiogenesis (Ferrandez et al, 2012). COX-2 expressing colorectal cancer tissues produces copious amounts of prostaglandin E2 (PGE2). As PGE2 causes resistance to apoptosis, stimulation of cell migration and angiogenesis, it has been implicated in the development and progression of various malignancies including those of the lung, breast and neck (Dixon et al, 2013). Human studies demonstrated that adenoma regression was more effective when PGE2 tissue levels were significantly inhibited by NSAIDs (Giardiello et al, 2004). Another study by Liao et al, 2012 discovered that COX-2 inhibition by aspirin downregulated phosphatidylinositol 3-kinase signalling, suggesting that regular aspirin use after colorectal cancer diagnosis led to increased survival among patients with mutated-PIK3CA tumours. Thus aspirin’s ability to reduce colorectal cancer occurs at least in part, via the inhibition of COX-2 activity.

Cox-independent mechanisms

In the face of mounting evidences, the contribution of COX-independent pathways to the anticancer effects of aspirin or its metabolite, salicylate cannot be discounted. Aspirin and salicylates have been found to inhibit IκB kinase (IKK) β and prevent NF-κB activation both in vivo and in vitro (Kopp and Ghosh, 1994; Yin et al, 1998; McCarty and Block, 2006). Till date, the only COX-independent target that is known to directly interact with aspirin or salicylic acid is IKK. Transcription of several proteins involved in inflammatory responses and angiogenesis is promoted by NF-κB (McCarty and Block, 2006); therefore, inhibition of this pathway may also contribute to the observed anticancer effects. However, some studies showed that aspirin-mediated induction of apoptosis in human colorectal cancer models requires activation of the NF-κB signalling pathway (Stark et al, 2007). It is possible that this differential effect may be related to the specific cell types and tissue environments. Aspirin has also been known to interfere with extracellular-signal-regulated kinase (ERK) signalling leading to its inhibition by preventing the binding of c-Raf with Ras in vitro (Pan et al, 2008). This observation is important because the ERK pathway is involved in cellular processes like proliferation, differentiation and survival. In view of the high levels of Ras mutations observed in many cancers leading to the activation of the ERK pathway (Bos, 1989), the finding that aspirin interferes with ERK signalling is very significant.

Aspirin can also affect mitochondrial functions. It increases the mitochondrial membrane permeability, causing the release of cytochrome c, resulting in the activation of caspases followed by cell apoptosis in several cell lines (Bellosillo et al, 1998; Zimmermann et al, 2000; Dikshit et al, 2006). Another mechanism includes the inhibition of mitochondrial calcium uptake by salicylic acid (Nunez et al, 2006) leading to anti-proliferative effects.

One of the major oncogenic pathways in colon cancer is the Wnt/β-catenin pathway. Aspirin is known to cause a concentration-dependent inhibition of this pathway in vitro (Bos et al, 2006). A recent study in colon cancer cells by Pathi et al, 2012 demonstrated that aspirin caused caspase-dependent proteolysis of Sp1, Sp3 and Sp4 (specificity protein) transcription factors, which was associated with downregulation of several Sp-regulated genes involved in cell survival, proliferation and angiogenesis. In another study, it was demonstrated that inhibition of 6-phosphofructo-1-kinase activity by aspirin and salicylic acid caused a decrease in glucose consumption and inhibition of cell proliferation (Spitz et al, 2009). Law et al showed that salicylate-induced cell growth arrest is associated with inhibition of p70s6k and downregulation of c-Myc, Cyclin D1, Cyclin A and proliferating cell nuclear antigen (Law et al, 2000). These reports indicate that the targets of aspirin and salicylates may directly or indirectly modulate the activity of transcription factors, cell signalling proteins, metabolic enzymes and mitochondrial proteins.

Extra-cox acetylation targets

Aspirin is mainly absorbed intact in the gastrointestinal (GI) tract (Leonards, 1962; Bridges et al, 1975) and later hydrolysed to the acetate and salicylate ions as it circulates in the plasma (Leonards, 1962). Hydrolysis can also occur during passage through the liver and other organs. It is well known that the acetyl group of aspirin can acetylate several proteins other than COX (Alfonso et al, 2009b; Marimuthu et al, 2011; Bateman et al, 2013). Experiments with radiolabelled 3H or 14C aspirin demonstrated that aspirin acetylates several proteins in vitro and in vivo through a transacetylation reaction (Hawkins et al, 1968; Caterson et al, 1978; Rainsford et al, 1983). Aspirin acetylates human serum albumin and fibrinogen in vitro and in vivo (Hawkins et al, 1968; Bjornsson et al, 1989). It can also acetylate several other proteins and biomolecules, such as haemoglobin, DNA, RNA, histones, transglutaminase as well as other plasma constituents including hormones and enzymes (Pinckard et al, 1968; Lai et al, 2010). In a remarkable study, it was found that in vivo administration of radiolabelled 3H or 14C aspirin to rats, led to the binding of the acetyl group of aspirin to several proteins, glycoproteins and lipids of the stomach, kidney, liver and bone marrow (Rainsford et al, 1983), demonstrating that the acetyl group is able to reach distant organs.

In a previous study, we demonstrated (Alfonso et al, 2009a) that aspirin acetylates the tumour suppressor protein, p53 at lysine 382 in MDA-MB-231 breast cancer cells. This acetylation was observed at the physiologically achievable concentration of 100 μM. MDA-MB-231 cells contain a mutant form of p53 (codon 280, Arg to Lys). This effect correlated with increased p53 DNA-binding activity and the expression of two of its target genes, p21CIP1 and Bax. Aspirin also acetylated p53 in other cell lines carrying different p53 mutations (unpublished data); however, it is not clear at this stage, if this changes the functional activity of p53. In view of the reports that, p53 is mutated and inactivated in 50% of all tumours, our observation that aspirin can acetylate mutant p53, is an important finding. Although further research is required, it is possible that acetylation of mutant p53 by aspirin, in some cases, may restore its DNA-binding properties leading to target gene expression. If this is the case, aspirin may curtail cancer cell growth through reactivation of mutant p53. In another study, using antibodies specific for the recognition of acetylated lysine residues, we found that aspirin acetylates multiple proteins in a dose-dependent manner in rat liver epithelial cells and HCT-116 colon cancer cells (Alfonso et al, 2009b; Marimuthu et al, 2011). In HCT-116 cells (Marimuthu et al, 2011), aspirin acetylated at least 33 different proteins, which included histones, cytoskeletal and heat shock proteins, glycolytic and pentose phosphate pathway enzymes and ribosomal and mitochondrial proteins. A detailed investigation on how the acetylation effects the functional activity of these proteins is yet to be conducted. It is to be noted that our study only identified proteins that are acetylated at lysine residues, as made possible by the use of the anti-acetyl lysine antibody and mass spectrometry. Aspirin can also acetylate proteins at serine and cysteine residues (Qin et al, 1993; Alfonso et al, 2009b; Bateman et al, 2013), but these acetylation events were not detected by our approach. In a recent report Bateman et al (2013) reported the ability of aspirin to acetylate 120 proteins in HCT15 human adenocarcinoma cells using an alkyne–aspirin chemical reporter. The identified enzymes included several metabolic pathway enzymes, structural proteins, proteins involved in translation, proteasomal subunits, mitochondrial proteins and histones. Among these, histones appear to be most intriguing owing to their prominent role in transcriptional regulation. Histone acetylation can cause charge neutralisation of basic lysine residues leading to changes in the chromatin structure and transcription of genes. It is possible that chemical acetylation by aspirin may have a role in shifting the equilibrium of the enzymatic acetylation/deacetylation process that occurs naturally in cells bringing about major changes in gene expression.

Studies show that aspirin is more effective in decreasing the incidence of colon cancer compared with the distal tissues (e.g., breast, lung, prostate, liver and skin). One possibility is that intestinal epithelial cells may be exposed to higher concentration of intact aspirin immediately following oral administration compared with the measured plasma levels, which reflects concentration after first-pass metabolism. A direct exposure of GI epithelial cells to higher concentration of intact aspirin may lead to greater degree of acetylation of proteins in the GI cells than the distal tissues. Plasma concentration of the intact aspirin at various doses following oral administration has been published; however, a similar estimation in the GI tract has not been reported. Future work is required to determine whether the significantly greater cancer risk reduction observed in GI tract is related to increased acetylation of proteins as compared with the distal tissues.

Chemical interactions of aspirin within the cell

Many natural products found in plants and bacterial cells have intrinsic reactivity properties as electrophiles (Drahl et al, 2005). Reaction with reactive small molecules, including cellular metabolites, damaged metabolic intermediates or exogenous agents can result in drastic rewiring of essential cellular processes, ultimately resulting in changes in cellular phenotype (Moellering and Cravatt, 2013; Wang et al, 2014). Although such interactions have been observed for quite some time, their effect on cancer cell biology is only recently being investigated in quite detail. The reactive nature of aspirins acetyl group (t1/2 in solution is 30 min) suggests that aspirin may also have off-target chemical reactions that can contribute to its biological effect.

Once aspirin enters the cell, a good portion of the compound is going to be quenched owing to hydrolysis reaction with aqueous solvent (Figure 1A). This reaction and others present an opportunity for high concentrations of salicylic acid in the cell, which may also interact with cellular molecules and disrupt their activity. Such an interaction has been described with NF-κB, an important transcription factor (Kopp and Ghosh, 1994).

Figure 1
Figure 1

Aspirin chemical reactivity. (A) Aspirin can easily enter cells and react with many different cellular chemicals. For example, aspirin can react with water to form the hydrolysis byproduct salicylic acid. Aspirin can also react with nucleophilic metabolites (e.g., glutathione) or proteins to produce acetylated products. (B) Aspirin can bind to enzyme active sites and modify nucleophilic functional groups. For example in COX-1 aspirin acetylates SER530, rendering the enzyme inactive. (C) Schematic of activity-based profiling to understand sites of acetylation on aspirin. In this experiment, aspirin acetylates active site nucleophilic amino acids. Then the pool of proteins is incubated with activity-based probes to reveal catalytically inactive functional groups, within the now-dead enzymes.

In addition to hydrolytic reactions, many reactive metabolites could, in principle, also react with aspirin. For example, thiol-containing glutathione can have an intracellular concentration in the millimolar range (Figure 1A) (Bennett et al, 2009). Glutathione’s near-neutral pKa and high reactivity would catalyse acetylation and quench its reactivity, thus taking away its ability to prevent oxidative stress (Arnold et al, 1995). Such interactions could remodel the cells metabolic profile and also have dramatic effects on stress-response pathways involving metabolite quenchers. At present, there is a lack of investigation into the alterations that aspirin has on the metabolic pool of the cell.

Recent evidence has shown that the introduction of electrophiles into the cell can alter enzyme activity by quenching lysine and cysteine reactivity (Wang et al, 2014). In these cases, the reactions of these molecules are enhanced by binding into active sites to lower the transition state and then reacting to quench activity. This is similar to aspirin’s role to render the COX enzymes catalytically dead (Figure 1A and B). However, additional examples, beyond the COX enzymes are severely limited. An exciting experimental platform to explore this possibility is activity-based profiling. In this way proteomes or cells would be exposed to concentrations of aspirin, allowing the chemical to react with protein side chains, covalently. Then, activity-based probes can be used to explore the changes in reactivity of active site-localised nucleophiles (Figure 1C). In this way, protein-reactive groups could be identified and enzymes whose activity is altered because of aspirin could be identified. Further, in many cases the targets of activity-based probes are already known (Simon et al, 2013), so this would also yield protein identification in one experiment. Some work has already demonstrated that there is widespread acetylation of biomolecules owing to aspirin’s reactivity (Marimuthu et al, 2011; Bateman et al, 2013). Therefore, there is a serious need to utilise optimised chemical and proteomic methods to interrogate the reactivity of both aspirin and salicylic acid.

Understudied potential targets of aspirin

A significant amount of research has been focused on the interactions of aspirin with proteins. Overall, these studies have revealed that aspirin’s reactivity can be increased by structural interactions that increase binding affinity for either steric blocking of enzymatic transformations, or the covalent acetylation of nucleophilic functional groups to render proteins enzymatically dead (Figure 2A). Nevertheless, the cell is composed of many different biologics, some of which are also inherently reactive and thus, may also sense aspirin and become modified.

Figure 2
Figure 2

Aspirin reactivity with RNA. (A) Aspirin reacts with serine hydroxyl groups in the active site of enzymes. This acetylation renders the enzyme inactive. (B) RNA acetylation can be performed by introducing electrophiles into cells. In this case reactivity of 2′-OH groups is facilitated by RNA structure and the proximity of the 2′-OH to the phosphate backbone. (C) Chemical reaction between aspirin and RNA, acetylating RNA 2′-OH groups.

Two understudied potential aspirin-interacting cellular molecules are RNA and metabolites. First, a significant portion of cellular mass is made up of RNA molecules. And, it has been shown that RNAs can become modified by exogenous chemicals introduced into the cellular milieu. Some of these compounds rely on RNA’s inherent reactivity as a nucleophile. RNA structure probes are a class of molecules that take advantage of RNA reactivity. For example, SHAPE (selective 2′ hydroxyl acylation and primer extension). In SHAPE, the reactivity of the 2′-hydroxyl in RNA is gated by local nucleotide flexibility (Merino et al, 2005). In other words, the 2′-hydroxyl is reactive at single-stranded and conformationally flexible positions but is unreactive at nucleotides constrained by base pairing. In solution, 2′-OH functional groups have pKa values that range from 12 to 14 (Velikyan et al, 2001). Nevertheless, it has been shown that RNA functional groups can alter their pKa values to approach biological conditions, and these changes are dependent on RNA structure (Ryder et al, 2001; Guo et al, 2009). SHAPE utilises electrophilic compounds that have carbonyl-carbon reactive centres, mostly anhydrides (Figure 2B). Such electrophilic centres are similar to those found in aspirin. Further, it has also been shown that certain 2′-OH groups can be hyper-reactive, owing to their intermolecular interactions with RNA functional groups nearby in space that transiently deprotonate the 2′-OH for activation (McGinnis et al, 2012). Overall, these studies hint that 2′-OH reactivity could be modulated to interact and catalyse an acetylation reaction with aspirin.

The biological consequences of RNA acetylation could be quite large (Figure 2C). For example, the 2′-OH is an important functional group in splicing (Fica et al, 2013). The binding of aspirin to the RNA and acetylation of an activated 2′-OH could in theory change the splicing pattern of a gene, therefore producing an alternative RNA isoform and protein product. Additionally 2′-OH groups have important roles in RNA structure and function (Moss, 2013). The acetylation of 2′-OH groups may alter the ability of a RNA to fold properly and ultimately result in an incorrect conformation and therefore disruption of biology. Lastly, it has been shown that RNA 2′-hydroxyl functional groups can have a role in the recognition of protein partners (Lunde et al, 2007). The capping of these interactions by aspirin could in principle alter the binding affinity or change the ability of the RNA to be sensed by an RNA-binding protein. These are just a few of the many potential biological consequences that RNA acetylation by aspirin could have on RNA biology and ultimately the many networks of a cell.

Small molecule metabolites have also been an understudied target of aspirin. Nevertheless, metabolites can be in some cases at millimolar concentration within certain cells (Bennett et al, 2009). Many such metabolites become altered by interactions with carcinogens and other exogenous agents. Therefore it seems plausible that the reaction of certain metabolites with aspirin could alter the metabolic landscape and have substantial effects on the biology of cells. Which metabolites would be so important and potentially reactive? One such molecule is Acetyl coenzyme A or acetyl-CoA. Acetyl-CoA is an important molecule in metabolism and is used for acetyl transfer reactions to many biological molecules. Its main function is to convey the carbon atoms within the acetyl moiety to the citric acid cycle (Krebs cycle). In chemical structure, acetyl-CoA is the thioester between the acyl carrier domain of the molecule and the coenzyme A (Figure 3A).

Figure 3
Figure 3

Potential of aspirin to acetylate Acetyl-CoA. (A) Chemical structure of acetyl-CoA. (B) Schematic demonstrating the possibility that aspirin acetylation keeps a high steady state level of acetyl-CoA in the cell, through a chemical recycling mechanism.

One of the most important functions of the acetyl-CoA donor is the regulation of chromatin state and therefore, transcription (Marmorstein and Roth, 2001; Marmorstein, 2001). One such potential way the acetylation of CoA could alter gene expression would be through chemical recycling of the acetyl-CoA in the cell (Figure 3B). This would thus increase or maintain a high steady state level of acetyl-CoA to serve as a substrate for acetyl transferase enzymes. Indeed, changes to acetylation status of many proteins have been tagged as an important process in neoplasm, depending on the target gene loci involved (Archer and Hodin, 1999; Wang et al, 2001; Kouraklis and Theocharis, 2003). Overall, the mere suggestion of acetyl-CoA activation by aspirin being an important alteration to the metabolic state of the cell is a rather intriguing possibility. Future efforts need to be extended to uncover novel targets of aspirin and aspirin-induced acetylation inside the cell.


Scientific evidence suggests that both constituent groups of aspirin that is, the acetyl and salicylate moieties have distinct targets that may together contribute to its anticancer effects. Although the acetyl group of aspirin did get its fair share of attention after the discovery of its mechanism of action through the inhibition of the COX enzymes in the 1970s, it has since been largely ignored. Acetylation is a unique characteristic of aspirin that is not shared with any other NSAID. Acetylation is also a critical endogenous posttranslational modification that affects the function of a wide array of proteins in the body (Choudhary et al, 2009). The ubiquitous nature of acetylation was demonstrated by Zhao et al, 2010, who showed that >1000 proteins are naturally acetylated in human liver cells. These included 44 metabolic pathway enzymes involved in glycolysis, fatty acid and glycogen metabolism, tricarboxylic acid and urea cycles. Acetylation has been associated with the control of enzyme activity by activating, inactivating or destabilising metabolic enzymes (Xu et al, 2013) and may allow cells to respond to changes in metabolic demands (Wang et al, 2010). Deregulated acetylation has been implicated in diseased states such as cancer (Xu et al, 2013) and therefore, identification of acetylatable targets of aspirin and modification in their function may shed light on the chemopreventive action of this drug. Aspirin’s ability to chemically acetylate endogenous proteins/biomolecules has immense therapeutic significance. Further research will provide a greater understanding of how the vast array of recently identified proteins/biomolecules acetylated by aspirin contributes to its chemopreventive properties.

Change history

  • 01 July 2014


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Support from the Translational Cancer Research Seed Grant, funded as 2010 Research Initiative Center by the State of South Dakota, and from NIH (5RO3CA133061-02) to GJB is gratefully acknowledged.

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  1. DYouville College School of Pharmacy, Buffalo, NY, USA

    • L Alfonso
  2. Department of Pharmaceutical Sciences, South Dakota State University College of Pharmacy, Brookings, SD, USA

    • G Ai
    •  & G J Bhat
  3. Department of Pharmaceutical Sciences, University of California, Irvine, CA, USA

    • R C Spitale


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Correspondence to G J Bhat.

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