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Chronic inflammation is a risk factor for colon cancer in patients with ulcerative colitis (UC). The molecular mechanisms linking inflammation and colon carcinogenesis are incompletely understood. We tested the hypothesis that TLR4 is involved in tumorigenesis in the setting of chronic inflammation.
Tissues from UC patients with cancer were examined for TLR4 expression. Colitis-associated neoplasia was induced using azoxymethane (AOM) injection followed by dextran sodium sulfate (DSS) treatment in TLR4-deficient (TLR4−/−) or wild-type (WT) mice. Inflammation, polyps, and microscopic dysplasia were scored. Cox-2 and PGE2 production were analyzed by real-time PCR, immunohistochemistry, or enzyme immunoassay. EGFR phosphorylation and amphiregulin production were examined by Western blot analysis and ELISA, respectively.
We show that TLR4 is overexpressed in human and murine inflammation-associated colorectal neoplasia. TLR4−/− mice were markedly protected from colon carcinogenesis. Mechanistically, we show that TLR4 is responsible for induction of Cox-2, increased PGE2 production and activation of EGFR signaling in chronic colitis. Amphiregulin, an EGFR ligand, was induced in a TLR4, COX-2-dependent fashion and contributes to activation of EGFR phosphorylation in colonic epithelial cells.
TLR4 signaling is critical for colon carcinogenesis in chronic colitis. TLR4 activation appears to promote the development of colitis-associated cancer by mechanisms including enhanced Cox-2 expression and increased EGFR signaling. Inhibiting TLR4 signaling may be useful in prevention or treatment of colitis-associated cancer.
Inflammation is considered a risk factor for many common malignancies including cancers of the lung 1, breast 2, and colon 3. Colon cancer is the third most common cancer and the third leading cause of cancer-related mortality in the United States 4. The link between inflammation and colon cancer offers the possibility of identifying novel ways to prevent cancer. However, the molecular mechanisms whereby chronic inflammation predisposes to cancer remain elusive.
The clearest link between inflammation and colon cancer is seen in patients with inflammatory bowel disease (IBD)5. Colorectal cancer is one of the most serious complications of IBD, accounting for increased mortality in these disorders 6. The severity of inflammation correlates with the risk of colorectal cancer in patients with IBD 7, 8. Consistent with a role of inflammation in colorectal neoplasia, animal models have demonstrated that the multi-functional transcription factor NF-κB is required for colorectal neoplasia 9. Therefore, focusing on the relationship between chronic inflammation and carcinogenesis may provide insights into the pathogenesis of colitis-associated cancer (CAC) and possibly sporadic colorectal cancer.
The colon contains 100 trillion bacteria, and commensal bacteria have been implicated in the development of sporadic colorectal cancer 10. Commensal bacteria may promote colorectal cancer by a variety of mechanisms including generation of reactive oxygen intermediates resulting in chromosomal instability 11. Bacteria are required for eliciting chronic inflammation and colon cancer in animal models of CAC 12, 13. Therefore, we have focused on TLR4 and its role in CAC. TLR4 is normally expressed at low levels in the intestinal mucosa 14–16 while it is up-regulated in patients with IBD 17. In acute colitis, we previously demonstrated that TLR4 is a potent inducer of cyclooxygenase-2 (Cox-2) expression 18. TLR4 may also be important for evasion of tumor surveillance 19. Altogether, these data raise the intriguing possibility that TLR4 promotes colon cancer in the setting of chronic inflammation, and this serves as the focus of the present study.
In the current study, we demonstrate first that TLR4 is over-expressed in human colon cancers arising in chronic ulcerative colitis. Over-expression of TLR4 was then confirmed in an animal model of inflammation-induced colon tumorigenesis wherein healthy, wild-type (WT) mice were given azoxymethane (AOM) to induce colonic neoplasia in the setting of chronic inflammation. Importantly, mice genetically lacking TLR4 were protected against colon tumorigenesis in this animal model of inflammation-induced carcinogenesis. Mechanistically, we show that TLR4 is required for expression of Cox-2 and enhanced PGE2 production in chronic colitis. TLR4-dependent tumorigenesis was also associated with activation of EGFR signaling. These findings are significant because both Cox-2 and EGFR have been linked to the development of colon tumors 20, 21. The current results provide important insights into the previously unrecognized role of TLR4 signaling in CAC and strengthen the rationale for developing chemopreventive therapies that target TLR4.
TLR4−/− mice were purchased from Oriental Bio Service, Inc. (Kyoto, Japan). All knockout mice were backcrossed to C57Bl/6J mice at least 8 generations. C57BL/6J mice were obtained from Jackson Laboratory as controls (Jackson Laboratory, Bar Harbor, Maine). Mice were kept in specific-pathogen free (SPF) conditions and fed by free access to a standard diet and water. All experiments were done according to Mount Sinai School of Medicine animal experimental ethics committee guidelines.
Following previously established methods for inducing colonic neoplasia 22, six to ten week old gender-matched mice were injected with 7.4mg/kg of AOM (Sigma, St. Louis, MO) intraperitoneally (i.p.) at the beginning of the experiment (day 0). After 14 days, mice were treated with 3% DSS (MW 36–50 kDa: ICN, Aurora, Ohio) in their drinking water for 7 days. This was followed by 14 days of normal water, another 7 days of 3% DSS treatment, and then normal water for an additional 14 days. During the DSS treatment and recovery phase, body weights, stool consistency, and stool occult blood were monitored, as described previously 23.
Mice were sacrificed on day 56. Colons were removed, opened longitudinally and stained with 1% Alcian Blue (Sigma, St. Louis, MO). High-resolution mucosal pictures were obtained using a Leica MZ APO dissecting microscope (Leica, Bannockburn, IL) with SONY Power HAD DXC-970MD 3CCD Color digital video camera, and Scion Image 1.60 image software (Scion Co., Frederick, MD). After macroscopic assessment, cecum, proximal, and distal parts of the colon were fixed in 10% buffered formalin, embedded in paraffin, sectioned and stained with hematoxylin and eosin. Histological assessment was performed by two independent gastrointestinal pathologists (R.X., H.C.) blinded to the mouse genotype and treatment. Severity of mucosal inflammation was graded using a standard scoring system (Table 1). Dysplastic lesions were determined by previously established criteria 24. To quantify the microscopic extent of dysplasia, paraffin-embedded colons were cut in 5 μm thick serial sections and every 20th section was analyzed for dysplasia. Number, size, and the percentage of the mucosal surface area containing dysplasia were determined under the microscope. The size of the lesions was calculated using a scale micrometer on the microscope.
The human colon cell line SW480 (1 × 106 cells/well) was maintained in Dulbecco’s modified Eagle’s medium supplemented with 2% heat-inactivated FCS, 2mM L-glutamine, penicillin/streptomycin and was incubated in 6-well plates overnight at 37 °C in a 5% CO2 humidified incubator. The next day, cells were incubated with Ultrapure lipopolysaccharide (LPS, 2μg/ml), Eschericha coli 0111: B4 (Invivogen, San Diego, CA) for varying time periods.
Total RNA was isolated using RNA Bee (Tel-Test, Inc., Friendwood, TX) according to the manufacturer’s instructions. A total of 1 μg RNA was used as the template for single strand cDNA synthesis utilizing the Transcriptor First Strand cDNA Synthesis Kit (Roche, Indianapolis, IN) according to the manufacturer’s instructions. Quantitative real-time PCR was performed for Cox-2, and β-actin using TaqMan probes. The primers and probes used in this study can be found on-line in Supplemental material. The cDNA was amplified using TaqMan universal PCR Master Mix (Roche, Indianapolis, IN) on an ABI Prism 7900HT sequence detection system (Applied Biosystems, Foster City, CA), programmed for 95°C for 10 minutes, then 40 cycles of: 95 °C for 15 seconds, 60 °C for 1 minute. The amplification results were analyzed using SDS 2.2.1 software (Applied Biosystems, Foster City, CA) and the gene of interest was normalized to the corresponding β-actin results. Data were expressed as fold induction relative to the lowest gene product amplified.
SW480 cells were plated at a density of 1.5 × 105 cells/well in 12-well plates 24hours before the first transfection. TLR4 small interfering RNA (siRNA) oligonucleotide corresponding to the sequence (GGUAAGGAAUGAGCUAGUAUU) was purchased from Dharmacon (Chicago, IL). Fifty nM of siRNA were transfected twice every 24 hours with X-trim gene siRNA transfection reagent (Roche, Indianapolis, IN) as per the manufacturer’s instructions. Forty-eight hours after the first transfection, cells were stimulated with LPS (2μg/ml) for the indicated period of time. Negative control siRNA (50 nM), which has no significant homology to any known gene sequences from mouse, rat, or human, was used as a control (Ambion, Austin, TX).
De-identified human colon resections were obtained under the auspices of the Mount Sinai Medical Center Institutional Review Board. Snap frozen tumor and surrounding colonic tissues from six ulcerative colitis patients, and actively inflamed colonic tissues from four ulcerative colitis patients undergoing colectomy were used. Mouse colon samples were taken at the time of sacrifice and frozen at −80°C. Details of tissue preparation and antibodies used for Western blot are included in Supplemental material. The mouse TLR4 band intensity was calculated using NIH image 1.62 by normalizing with the intensity of the corresponding β-actin band.
For the amphiregulin ELISA, SW480 (1 × 106 cells/well) were plated in 6 well plates. Cells were treated with LPS (2μg/ml) for the indicated periods. For ex vivo colonic tissue cultures, 100 mg of tissue from each part of the colon (not including the polypoid lesions) were cultured for 24 hours in 12 well flat bottom plates in serum free RPMI 1640. Supernatants were harvested for measurement of amphiregulin or TNF-α. ELISA (R&D Systems, Minneapolis, MN) was performed per the manufacturer’s instructions.
Paraffin-embedded human colectomy specimens of normal colon (n=11) (obtained from resection edge of sporadic colorectal cancers) or colitis-associated dysplasia or cancer (n=15; all patients with ulcerative colitis) were stained with biotinylated mouse monoclonal anti-human TLR4 (1:500, eBioscience, San Diego, CA) overnight at 4°C, followed by streptavidin-FITC (10 μg/ml, eBioscience, San Diego, CA) for 1 hour at room temperature. Details of staining methodology and antibodies used are found in Supplemental material.
Colonic tissue sections were examined for cell proliferation (bromodeoxyuridine: BrdU labeling) in the polypoid lesions as well as surrounding colonic mucosa. Mice were injected with 120 mg/kg of BrdU (Sigma, St. Louis, MO) i.p., 90 minutes prior to sacrificing, and colonic tissues was stained for BrdU using a BrdU staining kit (Zymed Laboratories Inc, South San Francisco, CA) according to the manufacturer’s instructions. The number of BrdU-positive cells per well-oriented crypt were calculated in every 3 crypts for each colon segment at high magnification under light microscopy.
For measurement of NF-κB activation, nuclear extracts were isolated from snap frozen mouse colonic tissues using a nuclear extraction kit (Active Motif, Carlsbad, CA) according to the manufacturer’s instructions. After measurement of protein concentration by the Bradford method, 1μg of nuclear extract was used to measure the DNA-binding activity of NF-κB p65 using TransAM NF-κB p65 Chemiluminescent kit (Active Motif, Carlsbad, CA) according to the manufacturer’s instructions. Chemiluminescent intensities were calculated as relative light units (RLU) and normalized with the mean RLU from untreated animals.
Production of PGE2 in the tissue culture supernatant was determined using a monoclonal EIA kit (Cayman, Ann Arbor, MI) according to the manufacturer’s instructions and as described previously 18, 25. Briefly, colonic samples from TLR4−/− and WT mice were washed in cold PBS containing penicillin, streptomycin, and fungizone (100U/ml each). 100 mg tissue fragments from the distal part of the colon closest to the anus were cultured for 24 hours in 12 well flat bottom plates in serum free RPMI 1640. Culture supernatants were harvested for PGE2 measurement.
Data were presented as mean (± SD). The significance was analyzed by Student t-test and Fisher’s exact test with Microsoft Excel and StatView software, respectively. P values were considered significant when < 0.05.
TLR4 expression is known to be low in the normal colon but increased in IBD 16, 26–28. We hypothesized that TLR4 is up-regulated in colitis-associated tumors. Colon tumor specimens from patients with UC with dysplasia or cancer were examined for TLR4 expression by Western blot analysis and immunofluorescent staining (Figure 1A, B). Non-dysplastic colon tissue from the same UC patients was used as a control. In addition, we examined samples from patients with active UC undergoing colectomy to assess the effect of moderate to severe inflammation on expression of TLR4. Non-dysplastic colon had low expression of TLR4 protein whereas samples of protein from the matched tumor specimens demonstrated higher expression of TLR4 (Figure 1A). Colon samples from active UC demonstrated expression of TLR4 comparable to the affected, non-dysplastic colon in UC cancer patients (Figure 1A). Immunostaining showed that, in normal colon, only cells at the base of the crypt and scattered cells in the lamina propria express TLR4 (Figure 1B). Colitis-associated tumors showed predominantly epithelial staining of TLR4 with varying degrees of TLR4 expression in cells of the lamina propria.
To further examine the role of TLR4 in colitis-associated tumorigenesis, we used a well-established model of CAC 24, 29. In this model, animals receive AOM, a genotoxic agent, followed by two cycles of DSS to induce inflammation. Using the AOM-DSS model, all WT mice developed polypoid or flat tumors. The microscopic features recapitulate the features of human dysplasia and polyps in colitis patients 30. We hypothesized that TLR4 expression would be increased in colorectal neoplasia in this CAC model. To investigate this possibility, we first examined mRNA expression of various TLRs in tumor tissues and surrounding non-dysplastic mucosa by real-time PCR (Table 2). Compared to the untreated colon, all TLRs examined demonstrated increased expression with inflammation. Of the TLRs tested, however, only TLR4 was increased in the tumor tissue compared with the surrounding inflamed mucosa. We then examined TLR4 mRNA expression under various conditions, e.g. untreated, acute DSS, chronic DSS (at day 56), AOM alone, AOM+DSS at day 56 (Figure 1C). Although TLR4 mRNA expression is increased following acute or chronic DSS compared with untreated mice, the highest level of expression was seen in tumors caused by AOM+DSS. Expression of TLR4 protein by Western blot was significantly elevated in tumors that developed in WT mice compared to the surrounding non-dysplastic mucosa (Figure 1D). Immunofluorescent staining for TLR4 also showed an increase in TLR4 expression in polypoid tumors (Figure 1E). Little TLR4 staining was seen in the normal epithelium or in the epithelium in chronic colitis. Muscularis propria stains for TLR4 consistent with a previous report 31. We conclude that colorectal tumors over-express TLR4 and that TLR4 may play a role in tumorigenesis.
To examine the role of TLR4 in colitis-associated tumorigenesis, we first addressed whether absence of TLR4 altered the susceptibility to developing CAC. TLR4−/− and WT mice were treated with AOM-DSS as described in Materials and Methods and developed weight loss and bleeding during DSS treatment (Figure 2A, B). We found a striking difference between WT and TLR4−/− mice with respect to development of polyps and dysplasia. All WT mice grossly showed multiple polypoid lesions but no such visible lesions were seen in TLR4−/− mice (Figure 2C). When examined microscopically, all WT mice (n=18) had at least one dysplastic lesion and up to 17 lesions per mouse (Figure 2C, D). In contrast, only five of eighteen TLR4−/− mice (27.8%) had one or two dysplastic lesions (Figure 2C, D). A significant increase in the number of dysplastic lesions was observed between WT and TLR4−/− mice (P < 0.001) (Figure 2D, Table 3).
The size and severity of dysplasia were also different between WT mice and TLR4−/− mice (Table 3). The few dysplastic lesions found in TLR4−/− mice were small, flat, and low grade. By contrast, 48% of dysplastic lesions (47/97) in WT mice were polypoid. BrdU staining of colon showed that proliferation was greatly increased in dysplasia and the surrounding epithelium of WT mice compared to non-dysplastic mucosa in TLR4−/− mice (Figure 2E). The number of BrdU positive cells was significantly higher in WT dysplastic (33.4 positive cells/100 epithelial cells ± 8.3SD) and non-dysplastic mucosa (20.4 cells ± 6.2SD) compared with the non-dysplastic mucosa in TLR4−/− mice (14.3 cells ± 3.8SD). These results demonstrate that TLR4 is required for initiation and growth of colorectal tumors in a mouse model of CAC.
Having demonstrated the link between TLR4 and colorectal tumors, we turned our attention to the mechanism by which this may occur. The severity of inflammation correlates with the risk of colorectal cancer in patients with IBD 7, 8. Using a scoring system for chronic colitis that examines features seen in human colitis, there was no significant difference between TLR4−/− and WT mice with respect to overall severity of colitis (Figure 3). A common connection between inflammation and carcinogenesis is the activation of signaling pathways that promote cell proliferation and increase cell survival such as the transcription factor NF-κB 9. TNF-α is a pro-inflammatory cytokine that is regulated by TLR-mediated NF-κB activation and has been linked to inflammation and carcinogenesis 32. Therefore, we examined transcriptional activity of NF-κB and TNF-α production in the colonic tissues from the CAC model. There were no significant differences in either NF-κB activation or TNF-α production between WT and TLR4−/− mice in the CAC model (Figure 3).
We reasoned, however, that inflammation at earlier time points might be different between WT and TLR4−/− mice. We have previously shown that following acute DSS treatment, TLR4−/− mice have significantly decreased recruitment of neutrophils 23. Although the total inflammatory scores following acute DSS treatment were similar between WT and TLR4−/− mice, there was a small but significant decrease in the sub-score for acute inflammation in TLR4−/− mice compared with WT mice (Figure 3B). Thus, we examined NF-κB activation and TNF-α production after seven days of DSS treatment. WT mice had significantly higher activity of NF-κB and increased production of TNF-α compared with TLR4−/− mice in the acute phase of colitis (Figure 3B). These results indicate that the decrease in inflammatory mediators such as NF-κB activation and TNF-α production in TLR4−/− mice may contribute to the subsequent protection from colorectal dysplasia. These data also highlight that in spite of expression of many other TLRs during inflammation (Table 2), the absence of TLR4 results in a decreased ability to mount a robust pro-inflammatory response.
Cox-2 is critical for development of colorectal neoplasia 20. We hypothesized that decreased expression of Cox-2 in TLR4−/− mice was associated with protection against tumorigenesis. Using real-time PCR, we found that mucosal Cox-2 expression was significantly decreased in TLR4−/− mucosa compared to WT mucosa in the CAC model (Figure 4A). Mucosal Cox-2 expression was found in lamina propria cells and to a lesser extent in IEC by immunofluorescent staining (Figure 4B). We confirmed by double staining that the majority of Cox-2 positive lamina propria cells were also positive for the macrophage marker CD68 (Figure 4C). We also performed double-staining of Cox-2 and a marker of myofibroblasts and found Cox-2-expressing myofibroblasts at the base of the crypts (Figure 4C).
Given that TLR4−/− mice have decreased expression of mucosal Cox-2 compared to WT mice, we investigated whether PGE2 production was also reduced. PGE2 production is important for both the formation and growth of colorectal tumors 33. We found that PGE2 production by colonic tissue from TLR4−/− mice was significantly less than in WT mice (Figure 4D). Given the well-established link between Cox-2 and colon carcinogenesis 20, these data suggest that TLR4 signaling may promote the development of CAC, in part, by inducing Cox-2 expression and PGE2 production.
Several studies have suggested that PGE2 stimulates colorectal carcinogenesis in part by activation of EGFR signaling 34, 35. We reasoned that TLR4−/− mice might be protected against colorectal carcinogenesis in chronic colitis because of decreased EGFR activation. Consistent with this hypothesis, levels of phosphorylated EGFR were significantly lower in colonic mucosa from TLR4−/− mice compared with WT mice (Figure 5A).
Additional studies were carried out to elucidate the mechanism by which activation of TLR4 stimulates EGFR tyrosine kinase activity. Amphiregulin, an EGFR ligand, is believed to play a role in colon carcinogenesis 36 and can induce COX-2 37. Hence, experiments were carried out to determine whether amphiregulin plays a role in TLR4-mediated activation of EGFR. Treatment with LPS caused a several-fold increase in production of amphiregulin in SW480 cells (Figure 5B). In contrast to nonspecific siRNA, LPS-mediated induction of amphiregulin was abrogated by siRNA to TLR4 (Figure 5C). We next addressed whether ligand binding was involved in LPS-mediated stimulation of EGFR tyrosine kinase activity. We found that antibody blockade of the EGFR ligand-binding site as well as a neutralizing antibody to amphiregulin abrogated LPS-mediated activation of EGFR (Figure 5D).
Given the compelling evidence that amphiregulin links the TLR4 pathway with activation of EGFR in human colonocytes, we hypothesized that TLR4−/− mice have reduced levels of amphiregulin in the colon. Mucosal amphiregulin release measured by ELISA was also significantly reduced in TLR4−/− mice compared with WT mice in the CAC model (Figure 5E). Collectively, these results strongly suggest that the reduction in EGFR tyrosine kinase activity in colonic mucosa from TLR4−/− mice (Figure 5A) is likely to be explained at least, in part, by reduced production of amphiregulin.
The present study establishes a molecular link between TLR4 and colon cancer in the setting of chronic inflammation (Figure 6). We demonstrate for the first time that TLR4 is highly expressed in colon cancers from patients with long-standing ulcerative colitis and in colonic tumors in a murine model of CAC. Our studies show a critical role for TLR4 in development of colitis-associated dysplasia since, in the absence of TLR4, colonic polyps do not occur. The ligand for TLR4, LPS, is abundant in the colonic lumen raising the intriguing possibility that colonic bacteria induce growth of colonic tumors through activation of TLR4. Chronic infection or chronic inflammation resulting in TLR4 activation may occur in other common malignancies, such as Helicobacter pylori and gastric cancer 38. In addition, hyaluronan, a non-bacterial TLR4 ligand present in chronically inflamed tissues, may activate TLR4 and contribute to carcinogenesis 39. Our results highlight the possibility of interfering with the host-microbial innate immune response to prevent or treat cancer.
NF-κB activation in both colonocytes and macrophages has been shown to be important in development of CAC and supports the connection between inflammation and colon cancer 9. In Greten et al.’s study examining the contribution of epithelial versus macrophage-dependent activation of NF-κB on colonic tumorigenesis, epithelial NF-κB activation was necessary for high tumor numbers whereas macrophage-dependent NF-κB activation contributed to tumor size. NF-κB can be activated by many upstream stimuli including TLRs. Our studies suggest that TLR4 may be a principal receptor, upstream of NF-κB, promoting the development of colonic tumors especially during the acute inflammatory stage. In our model, TLR4 expression is found in both epithelial cells as well as lamina propria mononuclear cells in neoplastic areas. In vitro, TLR4 can directly induce proliferation of IEC through EGFR activation 18. In vivo, there are likely to be multiple pathways leading to dysregulated epithelial proliferation in response to TLR4.
The intestinal epithelium is in intimate contact with the underlying lamina propria containing macrophages and subepithelial myofibroblasts; these cells have been shown to express TLR4 15, 16. Tumor-associated macrophages play a clear role in supporting tumor growth in a variety of systems 40. Some of the effects on the intestinal epithelium may be mediated by TLR4-dependent signals derived from the stroma. We show that Cox-2 expression and PGE2 levels are markedly different between WT versus TLR4−/− colons. Immunostaining demonstrates expression of Cox-2 predominantly in tumor-associated macrophages and myofibroblasts, but we know from our previous work that IEC also express Cox-2 in a TLR4-dependent way following acute injury 18. The finding of increased PGE2 production in our model is consistent with previous evidence of increased levels of PGE2 and deregulated expression of enzymes involved in the synthesis and catabolism of PGs in inflamed human colonic mucosa and colon cancers 41, 42. Recent work by Brown et al. demonstrates that mesenchymal stromal cells express Cox-2 and migrate to colonic epithelial progenitors during injury in a MyD88-dependent fashion 43. Without the migration of PGE2-producing stromal cells, epithelial proliferation is impaired. In addition, recent work demonstrates that bacteria can produce reactive oxygen intermediates that induce Cox-2 expression in macrophages leading, in turn, to chromosomal instability 11. These data highlight the interplay of bacteria and host cells in promoting colorectal cancer.
The reciprocal interaction between the epithelium and the stroma is complex. PGE2 can stimulate the release of EGFR ligands, such as amphiregulin 36. Thus, bioactive lipids produced by the stroma can amplify IEC proliferation through induction of trophic growth factors. At least in vitro, we show that amphiregulin is the principal contributor to EGFR activation. We have not shown, however, that the decrease in amphiregulin in TLR4−/− mice is the reason that EGFR activation is decreased. Likewise, EGFR signaling has been shown previously to increase Cox-2 expression and PGE2 secretion resulting in a positive feedback loop that contributes to deregulated cell proliferation44. More work is necessary to understand whether a positive feedback loop between EGFR and Cox-2 is at play in our model. In summary, several well-established mediators of human colon carcinogenesis, namely Cox-2, PGE2, and the EGFR, are modulated by TLR4 signaling.
For our studies, we have chosen the AOM-DSS model of CAC 24. AOM is a colonic genotoxic carcinogen that is extensively used for the investigation of colorectal carcinogenesis in rodents. Although by itself, AOM does not cause dysplasia or cancer in C57/BL6 mice, in combination with repeated cycles of DSS, it increases the incidence of dysplastic lesions 29. In particular, this model has been used to interrogate the inflammation-cancer link in the colon 9. Although no single animal model suitably reproduces all the features of human CAC, increased Cox-2 expression and enhanced PGE2 levels characterize this model and are reminiscent of human CAC 45.
Another question raised by our work is whether the effect of TLR4 is unique or whether other TLRs can contribute to development of malignancy. The colonic microbiota is diverse and should activate many TLRs. It is possible that other TLRs have the potential to induce dysplasia but that their contribution is weaker than TLR4. The prediction would be that the absence of all TLR signaling would also prevent colon cancer. We have evaluated whether CAC could be induced in MyD88−/− mice and all 15 mice succumbed from colitis following the first cycle of DSS (data not shown). MyD88−/− mice are fragile and may die as a result of sepsis, hemorrhage, or both, at least in part because MyD88 and TLR signaling are necessary for repair of the intestinal epithelium. It also suggests that targeting MyD88 as a therapeutic or chemopreventive intervention is likely to be impractical.
In summary, our results point to a critical role of TLR4 in development of colon cancer. Based on this study, we postulate that targeted inhibition of TLR4 may be effective in preventing development of colon cancer in IBD. TLR4 inhibitors are currently being evaluated in clinical trials of sepsis 46. One of the issues with the use of TLR4 antagonists is that our previous work suggests that during acute injury, TLR4 signaling is beneficial. Perhaps the value of TLR4 antagonists would be in patients with quiescent colitis with dysplasia or at high risk for dysplasia. Ideally, TLR4 signaling would be dampened but not eliminated. Cox-2 inhibitors are effective in reducing the risk of adenomatous polyps but unfortunately long-term use is associated with increased cardiovascular complications 47, 48. Therefore, new approaches to preventing colon carcinogenesis are required. Our studies will permit rational therapies to be developed that combine blockade of TLR4 and other signaling pathways, such as EGFR signaling, in the prevention or treatment of CAC.
Supported by NIH grants AI052266 (MTA), DK069594 (MTA), CA111469 (KS), Career Development Award from CCFA (MF), Uehara Memorial Foundation Research Fellowship (MF), and the New York Crohn’s Foundation (AJD).
The authors have no conflicts of interest to disclose.
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