Gut microbiota and colorectal cancer
© The Author(s) 2016
Received: 21 January 2016
Accepted: 29 March 2016
Published: 1 June 2016
The mucosal immune system is unique to the gastrointestinal mucosa, in which a large number of immune cells are located and exert multiple functions. Meanwhile, ~100 trillion microorganisms are thought to co-inhabit in the gastrointestinal tract. Furthermore, immune cells and gut microbiota have a mutual influence and the maintenance of this symbiotic relationship results in gut homeostasis. A recent study suggested that a disturbance of gut microbiota—so called “dysbiosis”—is related to various diseases, such as inflammatory bowel disease (IBD) and colitis-associated cancer (CAC). In this review, we discuss the relationship between gut microbiota and the mucosal immune system with regard to the development of IBD and CAC. In addition, we elucidate the possibility of probiotics in treatment against these diseases.
KeywordsGut microbiota Colorectal cancer Colitis-associated cancer Mucosal immune system Dysbiosis
The mammalian gastrointestinal tract, where digestion and absorption occurs, acts as the frontline of defense against microorganisms from the environment. Therefore there is an established unique immune surveillance system called the mucosal immune system. It is supposed that a half of immunocompetent cells reside in the gut mucosa, and the balance between them with a variety of properties, including T helper 17 (Th17) cells and regulatory T (Treg) cells, is thought to be controlled exquisitely. Characteristics of the mucosal immune system are represented by their contrasted immune functions, such as the removal of pathogens and immune unresponsiveness to the food antigens and indigenous gut microbiota. Increasing evidence suggests that the gut microbiota also plays key roles in homeostatic maintenance of the mucosal immune system. Imbalance of gut microbiota, so called “dysbiosis”, based on dysregulation of the mucosal immune system affects the development and pathogenesis of various diseases such as allergy, diabetes, autoimmune diseases and cancer [1, 2]. In addition, a recent finding has suggested that when feces of healthy adults were intra-rectally inoculated into patients with recurrent Clostridium difficile infection, the symptoms improved in association with the recovery from dysbiosis , which would be a clear example of gut microbiota contributing to restraint of colonic inflammation. Furthermore regarding the onset of inflammatory bowel disease (IBD) and colitis-associated cancer (CAC), the interaction between the mucosal immune system and gut microbiota is important, because in germfree animal models of these diseases, no symptoms are observed [4, 5]. In this review, we discuss the roles of gut microbiota and the mucosal immune system on the development of IBD and CAC.
Gut microbiota in IBD
IBD is categorized into Crohn’s disease (CD) and ulcerative colitis (UC) based on pathophysiological characteristics. UC is an inflammatory disease confined to the colonic mucosa, whereas CD has the potential to develop along the entire gastrointestinal tract with a higher occurrence in the small and large intestines. Because both diseases exhibit repeated remission and relapse, it is important that we urgently improve the quality of life of patients with IBD. In accordance with the development of an analytical method, based on bacterial 16S rDNA and next generation sequencing (NGS), the characteristics of gut microbiota in patients with IBD are rapidly being elucidated. A loss of bacterial diversity and dysbiosis is present in the gut microbiota of patients with IBD, as commonly detected using NGS. In particular, there is a marked decrease in the occupancy of Firmicutes and Bacteroidetes in gut microbiota, which normally predominates in a healthy adult. It has been reported that 46 strains of Clostridium derived from mice and 17 strains of Clostridium derived from humans induced differentiation of Foxp3+ Treg cells, resulting in mass production of IL-10, via augmentation of TGF-β provided by colonic epithelial cells [6, 7]. It was then demonstrated that Clostridium butyricum when used as a probiotic, could induce IL-10 production from macrophages in colonic mucosa, which resulted in suppression of acute colitis in mice . It has been discussed that butyrate participated in suppression of colitis and colorectal cancer. The bacterial metabolite, butyrate, induces the differentiation of colonic Foxp3+ Treg cells and ameliorates the development of colitis. A possible mechanism for this regulation of differentiation may be that butyrate enhances histone H3 acetylation in the promoter and conserved, non-coding sequence regions of the Foxp3 locus . Because the occupancy of Clostridium clusters IV and XIVa, in which numerous butyrate-producing bacteria exist, have been shown to be decreased in the gut microbiota of patients with IBD, it would be expected that clinical applications of these results would follow.
With regard to the interaction of the mucosal immune system and gut microbiota, secretory immunoglobulin A (IgA) is important. The presence of secretory IgA in the intestinal lumen is indispensable for the exclusion of pathogenic germs and neutralization of toxins. Germ-free mice have few IgA-producing cells in their intestinal mucosa. Total bacterial numbers increase markedly in the mice deleted activation induced cytidine deaminase (AID) gene, which is normally essential for somatic hypermutation and class switch recombination during IgA gene rearrangement. IgA produced in inhibitory receptor of immune system (programmed cell death-1 (PD-1)) gene-deficient mice had a low affinity for bacteria, which caused alterations of microbial communities in the gut . In addition, it has been recently reported that some gut microbiota was coated with IgA, and IgA-coated fecal bacteria taken from patients with IBD exacerbated dextran sulfate sodium (DSS)-induced colitis in gnotobiotic mice .
Gut microbiota in colorectal cancer
Colorectal cancer is one of the most common fatal malignancies in the world. The involvement of gut microbiota in the development of colorectal cancer has been noted for some time. IL-10-deficient mice and TCRβ/p53 double knockout mice do not develop colorectal cancer under germfree environment, providing a rationale for the association between colorectal cancer and gut microbiota . Chronic inflammation is known to predispose an individual to cancer, and as such, the presence of IBD increases the risk of colorectal cancer. Another such example would be CAC. The molecular mechanisms underlying the pathogenesis of CAC are unclear and do not follow the adenoma-carcinoma sequence . It is urgent to clarify the mechanism underlying development of CAC, because ~20 % of patients with chronic inflammation in the form of UC develop CAC within 30 years from the onset, with at least half of the cases resulting in death. A recent study demonstrated that dysbiosis of gut micobiota plays a key role in the pathophysiology of CAC. Bacterial diversity is remarkably decreased in gut microbiota of sporadic colorectal cancer and CAC mice models. When gnotobiotic mice are colonized with feces taken from sporadic colorectal cancer or CAC mice, the incidence and number of tumors are increased in both cases, compared with those colonized with feces of healthy mice. CAC can be experimentally induced in rodent models by the combination of introduction to azoxymethane (AOM) and repeated exposure to the inflammatory agent DSS. Results from time-course analysis of the composition of gut microbiota during development of CAC in this model indicated tumor-bearing mice showed enrichment in operational taxonomic units (OTUs) affiliated with members of the Bacteroides, Odoribacter, and Allobaculum genera and decreases in OTUs affiliated with members of the Prevotellaceae and Porphyromonadaceae families. Furthermore, conventionalization (colonization of germfree mice with gut microbiota) with tumor-bearing mice significantly increased colon tumorigenesis compared to those colonized with feces of healthy mice . However, mice exposed to the chemical mutagen do not develop tumors if they receive antibiotics and mice that received feces of tumor-bearing mice do not develop tumors if they are not exposed to the mutagen. These findings suggest that gut microbiota plays a part in the initiation of colorectal cancer. CAC results from the complex relationship between chronic inflammation and dysbiosis of gut microbiota, which would induce irreversible changes to intestinal epithelial cells. Bacteroides fragilis toxin, produced by enterotoxigenic B. fragilis (ETBF), triggers colorectal cancer by binding to colonic epithelial cells and stimulating cleavage of the cell adhesion molecule E-cadherin, which act as the tumor suppressor protein . Antibody-mediated blockade of interleukin-17 (IL-17), a key cytokine for proinflammatory responses, inhibits ETBF-induced colitis and tumor formation . Gut microbiota of IL-10 deficient mice developing spontaneously severe colitis have decreases in bacterial diversity and increases in the occupancy of Enterobacteriaceae . IL-10 deficient mice colonized with either Escherichia coli (E. coli) or Enterococcus faecalis develop colon inflammation, but only the mice receiving E. coli developed colon tumors. Moreover, it was reported that Colibactin, the product of polyketide synthase (pks) in E. coli NC101, cleaved double stranded DNA in colonic epithelial cells and promoted invasive carcinoma in AOM-treated IL-10deficient mice . Because the expression of the ETBF toxin gene and pks gene of E. coli NC101 is higher in patients with colorectal cancer when compared to healthy adults, aberrant proliferation of these bacteria caused by dysbiosis of gut microbiota would induce disruption of epithelial barrier function and contribute to the mechanism of CAC development. However, there is some uncertainty, because the murine AOM/DSS model administered microbes from patients with colorectal cancer developed unexpectedly fewer tumors than those that received bacteria from healthy human donors . Therefore, we would need to validate the evidence, accumulated by studies using animal models of colorectal cancer, in human. Furthermore, it has also been revealed that the role of gut microbiota in cancer extended to treatment, influencing not only the effectiveness of chemotherapy but also its side effects. Both germfree mice and antibiotic-treated mice show cyclophosphamide resistance and in these mice, pathogenic Th17 cells are shown to be decreased . Taken together, it is likely that modulating the gut microbiota will become an effective tool to combat colorectal cancer.
CAC and IL-6/Stat3 pathway
Probiotics as prevention for IBD/CAC
Reverting the disturbances of gut microbiota in patients with IBD and CAC, as previously mentioned, should become the new strategy for treatment. Although several clinical trials using probiotics for patients with IBD have been performed in Japan and overseas, the clinical effects are dependent on the probiotic strain and the schedule of probiotic administration. In the trial for the patients with mildly to moderately active UC received one of the probiotic Lactobacillus strains, Lactobacillus casei strain Shirota (LcS), daily for 8 weeks, significantly better clinical activity index scores were seen after LcS treatment compared with pre-treatment and control group values . In the trial for people at high-risk of developing colorectal cancer, they were administered wheat bran, LcS, both or neither. Incidence of tumors with a grade of moderate or high atypia was significantly lower in the group administered LcS than the other groups. No significant difference in the development of new colorectal tumors was observed with administration of either wheat bran or LcS . After 1 year of treatment with Bifidobacterium breve strain Yakult and galacto-oligosaccharides symbiotics, the clinical status was significantly improved, and the amount of myeloperoxidase in the lavage, the number of Bacteroidaceae in feces and fecal pH was reduced in the patients with mild to moderate UC . We had reported previously that LcS has the protective efficacy against CAC . LcS suppressed the development of CAC by suppressing IL-6 trans-signaling in a murine CAC model, whereas polysaccharide-peptidoglycan complex 1 (PS-PG1) deficient LcS strain had no effect on the prevention of CAC (Fig. 2d). It was also revealed that this effect of LcS was accompanied with improvement of dysbiosis of gut microbiota. As recently reported, transplant of fecal microbiota from healthy individuals is effective in treatment. However transplant of feces requires considered attention in patients with benign disorders, such as IBD, because there is a possibility of accidental contamination with unknown infectious diseases. By avoiding this, probiotics have guaranteed safeguards against such events. Therefore amelioration of dysbiosis by using probiotics could be a potent tool implemented as a new medical treatment for these diseases as well as their prevention.
Gastrointestinal mucosa has a unique immune system, in which many immune cells reside and exert multiple functions. Those immune cells and gut microbiota have a mutual influence on immune response. Recent studies suggested that an imbalance of gut microbiota—“dysbiosis”—is related to the condition of patients with not only gastrointestinal diseases but also other diseases. It is estimated that dysbiosis of gut microbiota plays an essential role in the initiation of IBD and CAC. The strategy of recent studies on IBD and CAC is altering, which aimed at remedying dysbiosis by considering gut microbiota as “a microbial community effect” from studies focused on individual enterobacterial roles. Dysbiosis of gut microbiota presumably induces the change in the enteric environment that leads to mucosal inflammation or tumorigenesis. It will be necessary to accumulate a scientific overview for the interaction of gut microbiota and the mucosal immune system in the future, to utilize the improvement of the gut microbiota as a mode of treatment in the development of new cures for IBD and CAC.
activation induced cytidine deaminase
dextran sulphate sodium
enterotoxigenic Bacteroides fragilis
inflammatory bowel disease
intestinal epithelial cell
Lactobacillus casei strain Shirota
operational taxonomic units
programmed cell death-1
polysaccharide-peptidoglycan complex 1
suppressor of cytokine signaling 3
signal transducer and activator of transcription 3
TNFα converting enzyme
We would like to thank Dr Stefan Rose-John and Dr Keiichi Mitsuyama for their valuable support on this manuscript.
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