Intestinal microbiota: a novel perspective in colorectal cancer biotherapeutics

Abstract

It is believed that genetic factors, immune system dysfunction, chronic inflammation, and intestinal microbiota (IM) dysbiosis contribute to the pathogenesis of colorectal cancer (CRC). The beneficial role played by the direct regulation of IM in inflammatory bowel disease treatment is identified by the decreased growth of harmful bacteria and the increased production of anti-inflammatory factors. Interestingly, gut microbiota has been proven to inhibit tumor formation and progression in inflammation/carcinogen-induced CRC mouse models. Recently, evidence has indicated that IM is involved in the negative regulation of tumor immune response in tumor microenvironment, which then abolishes or accelerates anticancer immunotherapy in several tumor animals. In clinical trials, a benefit of IM-based CRC therapies in improving the intestinal immunity balance, epithelial barrier function, and quality of life has been reported. Meanwhile, specific microbiota signature can modulate host’s sensitivity to chemo-/radiotherapy and the prognosis of CRC patients. In this review, we aim to 1) summarize the potential methods of IM-based therapeutics according to the recent results; 2) explore its roles and underlying mechanisms in combination with other therapies, especially in biotherapeutics; 3) discuss its safety, deficiency, and future perspectives.

Introduction

Colorectal cancer (CRC) is one of the leading causes of cancer mortality in the world,¹ being ranked fifth most lethal neoplasia in China.² In 2015, the National Cancer Center of China estimated that approximately 489,000 new CRC cases will be diagnosed in China, with more than 246,000 Chinese expected to die of it.² The pathologic process of CRC is from normal epithelium to adenomatoid polyps, and finally to adenocarcinoma. Depending on its etiology and pathogenesis, CRC mainly divides into sporadic, hereditary, and inflammatory CRC. As part of a multistep process, genetic factors, life styles, diet habits, and chronic inflammation are thought to contribute to the occurrence and progression of CRC through the accumulation of a variety of genetic and epigenetic alterations.^3–7 Notably, a number of studies have shown that the 5-year accumulative cancerization risk of inflammatory bowel disease (IBD) is up to 33%–54%.^8–10 In addition, patients with IBD have an increased 2–4 times risk of developing CRC than the normal.¹¹ Although multiple mutations are needed for both inflammatory and sporadic CRC, IBD-CRC model could accelerate hypermethylation, and chromosomal and microsatellite instability, and alter the stability and diversity of intestinal microbiota (IM).^6,10,12 It is widely identified that intestinal bacteria dysbiosis is associated with the loss of epithelial barrier function, the pathogenesis of IBD, and colitis-associated CRC.^13,14

Human intestinal microbes contain at least 1,000 species, which are essential for digesting food, controlling intestinal epithelial homeostasis, intestinal development, and human health.¹⁵ Intestinal mucosal symbiotic bacteria increase intestinal stability and inhibit intestinal colonization by pathogens. When the balance of IM is broken, intestinal mucosal barrier and innate immunity function are reduced, and the relative pathogenic factors are increased so as to cause chronic inflammatory and infectious diseases. Interestingly, a new study indicated that IBD susceptibility is attributed to specific bacteria communities and that manipulation of the IM alters the induction and/or perpetuation of T-cell-induced colitis.¹⁶ The important modulation role of gut microbiota in inflammation-induced tumorigenesis was evident through the inhibition of tumor formation found in several CRC mouse models.^17,18 In addition, numerous bacterial species such as Bacteroides fragilis, Fusobacterium nucleatum, and Peptostreptococcus stomatis have been found to have significant association with human CRC samples.¹⁹ A study first assessed that fecal microbiota also could directly promote intestinal carcinogenesis in germ-free mice and mice given a carcinogen through gavage of stool samples from patients with CRC.²⁰ More recently, tumor-prone mice cocolonized with enterotoxigenic B. fragilis (ETBF) and Escherichia coli (expressing colibactin) showed increased levels of inflammation markers in the colon and DNA damage in colonic epithelium with faster tumor onset and greater mortality, compared to mice with either bacterial strain alone.²¹ Mechanistically, gut microbiota may induce CRC by numerous processes, including the generation of toxic metabolites and genotoxic biosynthesis, the changes in DNA damage and chromosome instability, and an effect on epithelial cells proliferation and apoptosis.^22–24 However, the accurate molecular mechanism of gut microbiota-induced CRC remains unknown. “Alpha-bug”,²⁵ “Driver-passenger”,²⁶ and “Integrated function”²⁷ are the three major carcinogenic theories for IM-mediated CRC. Among these patterns, Gallimore and Godkin perfectly described the combined reaction of gut microecology, chronic inflammation, and intestinal mucosal barrier in the occurrence and progression of CRC.

At present, the radical surgery is the only probable cure for CRC, but the overall outcome for local and distant metastatic patients is barely ameliorated. Traditional chemo/radiotherapies have improved the survival rate of these patients, and reduced the recurrence rate in a certain extent.²⁸ However, researchers must develop alternative methods or drugs to combat the problem that, due to long-term chemo-/radiotherapy, an increasing number of patients have the serious therapy resistance and the occurrence of cancer metastasis. Notably, ~35% of patients with CRC have metastatic disease at diagnosis, which is a major cause of CRC-associated mortality.²⁹ Obviously, the prevention and early diagnosis is of great significance in the treatment and prognosis of CRC patients. Chronic inflammation is an important risk factor for intestinal carcinogenesis. Thus, effective prevention and/or treatment of IBD can significantly reduce the incidence of colitis-associated CRC. Probiotics and fecal microbiota transplantation (FMT) are being increasingly employed to treat IBD through the direct regulation of gut microbiome. In addition, probiotics and FMT can enhance the secretion of anti-inflammatory factors, reduce the growth of harmful bacteria by reconstructing intestinal mucosal barrier and immune system function, and thus play a preventive and therapeutic role in IBD.^30,31 Currently, probiotics and FMT have been regarded as a safe treatment strategy compared to traditional treatment with significant toxicity, high recurrence rates, and poor outcomes. Exhilaratingly, a recent study demonstrated for the first time that patients with gastric carcinoma exhibit a dysbiotic microbial community with genotoxic potential, which is distinct from that of patients with chronic gastritis.³² Besides, present studies indicated that the structure and characteristics of the gut microbiota are markedly altered in CRC. Further population-based epidemiologic study is necessary to reveal the characteristics of intestinal microbiome in ultraearly CRC, which might provide some novel prophylactic and early diagnosis strategies for CRC patients.

Different from the traditional treatments, biotherapeutic is a new avenue to target cancer mainly through mobilizing the body’s natural anticancer ability and restoring the balance of the internal microenvironment. Until now, numerous studies have been successfully conducted for IM-based CRC therapies in animal models by using pro-/prebiotics.^33,34 Additionally, targeted gut microbiome might be an effective strategy for preventing the progression of inflammation-driven CRC under antibiotic treatment.³⁵ Moreover, IM has been found to play a significant modulation role in immune-checkpoint inhibitors-mediated anticancer immune response.^36,37 In clinical trials, pro-/prebiotics are widely used to reduce postoperative infections, and improve bowel immune system and epithelial barrier function in CRC patients.^38–40 Meanwhile, it has identified that the specific intestinal bacteria could affect chemo-/radiotherapy sensitivity in CRC patients.^41,42 Based on these evidences, IM turns out to be encouraging in clinical application and shows a promising target in CRC biotherapeutics. Here, we mainly review our emerging understanding of IM-based therapies in current applications for CRC patients, and discuss its potential in biotherapeutics. The general concerns of IM-based CRC therapies include underlying methods, the novel roles in combination with other treatments, especially in immunotherapy, and analysis of safety, efficacy, and future perspectives.

IM is closely linked to CRC pathologies

Recently, it has been demonstrated that gut microbiota contributes to the development of CRC through altering intestinal bacterial biofilms, microenvironment homeostasis, and immune reaction. Bacterial biofilms consist of a higher-order level of spatial organization of multi-organism structures in mucosal microbial communities in the human intestine, and act as the first line of defense against invading microbes-induced inflammatory responses and the production of genotoxic bacterium-derived compounds.^43–45 Alteration of colonic mucosal biofilms in the colon tissue microenvironment is a distinct feature of proximal CRC.⁴³ Bacterial biofilms were associated with diminished colonic epithelial cell E-cadherin and increased crypt epithelial cell proliferation in normal colon mucosa.⁴³ Comparative researches of the stool samples of healthy individuals and CRC patients found a significant difference in bacterial genera.^19,46 It had shown that a reduction of biodiversity and richness of microbial community with an increase in Fusobacterium, Peptostreptococcus, Bacteroides, Eubacterium, Proteobacteria, Prevotella, and Clostridium species were associated with CRC patients.^19,46–50 Among these bacteria, F. nucleatum was found to contribute to serrated pathway, adenoma–carcinoma sequence, and pathologic progression in CRC.^51,52 Further study had identified that F. nucleatum promoted proliferation of CRC cells and tumor development in mice by activating toll-like receptor (TLR)/myeloid differentiation primary response gene 88 (MyD88)/nuclear factor-κB signaling.⁵³ Notably, infection with F. nucleatum animalis in colorectal tissue could induce inflammatory response and promote CRC development.⁵⁴ In addition, F. nucleatum had been shown to expand myeloid-derived immune cells, which suppressed T-cell proliferation and induced T-cell apoptosis in CRC.⁵⁵ These results suggest that gut microbiota plays a great role in the initiation and progression of CRC.

Potential therapeutics for IM

Oral probiotics

Probiotics are live microorganisms, which confer a beneficial role in cancer prevention and treatment by reducing harmful bacterial translocation, promoting intestinal immune barrier function and antipathogenic activity.^56,57 Currently, Lactobacillus, Bifidobacteria, Saccharomyces boulardii, and Bacillus coagulans are the most common products of microbiota used as probiotics.^56,57 In addition, synbiotics, as a conjunction between prebiotics and probiotics, are used to improve the survival of the probiotic bacteria during the passage through the upper intestinal tract.⁵⁶

Several studies had indicated the intelligible effects of the cytoplasmic extracts or cell-free supernatants from probiotic products or strains in inhibition of CRC cells proliferation and prevention of malignant transformation in vitro.^58–60 Notably, a recent paper⁶¹ had revealed that the combined application of Propionibacterium freudenreichii and tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) increased proapoptotic gene expression and decreased antiapoptotic gene expression in CRC cells, suggesting that P. freudenreichii has potential as a new adjuvant for TRAIL-based CRC therapy. In experimental models, probiotics could obviously decrease the incidence and development of carcinogen-induced CRC.^33,62–67 Interestingly, two reports demonstrated that probiotics exhibited an inhibitory role against colorectal tumorigenesis in adenomatous polyposis coli mutation mice.^68,69 In addition, murine models of colorectal carcinoma fed with the engineered microbes and the cruciferous vegetable diet displayed significant tumor regression and reduced tumor occurrence.⁷⁰ In CRC patients who were submitted to surgery, oral probiotics effectively reduced the tumor recurrence rate, and protected the intestinal mucosa physical and biologic barrier.^71,72 According to the researches, either dietary synbiotics or yogurt attenuated the CRC risk factors.^40,73 Moreover, it had demonstrated that Lactobacillus casei could prevent atypia of colorectal tumors.⁷⁴ To date, 24 clinical trials of pro-/synbiotics therapies had been published and shown a favorable benefit for CRC patients (Table 1). The outcomes of these studies are highlighted as a possible alternative or adjuvant to conventional methods in CRC therapeutic.

Table 1.

Clinical applications and outcomes of pro-/synbiotics formulations in CRC therapy

Pro-/synbiotics	Outcome	Subjects	Reference
Lactobacillus rhamnosus, Bifidobacterium lactis, inulin	A reduction of colorectal proliferation and an improvement of epithelial barrier function	CRC and polypectomized patients	40
Lactobacillus casei	Preventing atypia of colorectal tumors	CRC removed patients	74
Lactobacillus, Bifidobacterium, Thermophilus, Enterococcus faecium	A feasible approach to protect patients against the risk of therapy-induced diarrhea	Chemo-/radiotherapy CRC patients	75–77
Bifidobacterium, Lactobacillus acidophilus Lactobacillus, Pediococcus pentosaceus,	A beneficial effect on the intestinal barrier function and a reduction of infection complication	Preoperative therapy of CRC patients	78–80
Leuconostoc mesenteroides, fermentable fibers	A beneficial effect on the intestinal barrier function and a reduction of infection complication	Preoperative therapy of CRC patients	81
Lactobacillus, Bifidobacterium, E. faecium, Saccharomyces boulardii	An improvement of gut mucosal barrier and a reduction of infectious complications	Perioperative therapy of CRC patients	71, 82–86
P. pentosaceus, L. mesenteroides, Lactobacillus, multiplant fibers	A protective effect in preventing a postoperative inflammatory response	Perioperative therapy of CRC patients	87
Lactobacillus, Bifidobacterium, Streptococcus thermophiles, oligofructose	A reduction in the prevalence of fecal enterobacteriaceae and bacterial translocation, but not in inflammatory response or septic morbidity	Perioperative therapy of CRC patients	88
Lactobacillus, Bifidobacterium, fruit oligosaccharides	An increased production of interferon-gamma, and minor stimulatory effects on the systemic immune system	Postoperative therapy of CRC patients	38
Lactobacillus, Bifidobacterium, fruit oligosaccharides	A beneficial effect of symbiotic supplementation, and CRP reduction in meantime	Postoperative therapy of CRC patients	89
Lactobacillus plantarum, L. acidophilus-11, Bifidobacterium longum-88	A reduction of the serum zonulin level, the rate of postoperative septicemia, and a maintainment of the liver barrier	Perioperative therapy of colorectal liver metastases	90
E. faecium M-74	An effective and promising method for elimination of pathogenic bacteria in the case of IBD and CRC	CRC and IBD patients, healthy subjects	91
Bifidobacterium triple viable capsule	An inhibited role in small intestinal bacterial overgrowth with alleviating its symptoms	Gastric cancer and CRC patients	92
Lactobacillus, Bacillus natto	An improvement of bowel symptoms and quality of life	Postoperative therapy of CRC, and CRC survivors	39, 93

Abbreviations: CRC, colorectal cancer; IBD, inflammatory bowel disease; CRP, C-reactive protein.

However, four clinical reports indicated that pro-/synbiotics had no measurable effect on gut barrier function, inflammatory response, and complications after CRC surgery.^94–97 In addition, although synbiotic supplementation with Bifidobacterium lactis and resistant starch induced unique changes in fecal microflora, it did not significantly alter any other fecal, serum, or epithelial biomarkers of CRC patients.⁹⁸ These results allow us to consider the patient’s family history and lifestyle, including diet, smoking, and other factors before treatment with pro-/synbiotics. In line with the above comment that further and in-depth researches are taken to gain a keen understanding of their clinical value in CRC patients.

Providing prebiotics

In 2016, the International Scientific Association for Probiotics and Prebiotics had updated the definition of a prebiotic: a substrate that is selectively utilized by host microorganisms conferring a health benefit, not confined to traditionally considered fructans (fructooligosaccharides and inulin) and galactans (galactooligosaccharides)-based carbohydrate.⁹⁹ This new definition will help broaden the scope of prebiotics in research studies and clinical applications. Despite that both prebiotics and probiotics can improve the integrity of the epithelial layer of the intestines, they can also increase the resistance against pathogenic colonization, a completely different model. Probiotics as new bacteria enter the human intestinal tract and then improve intestinal microecology, while prebiotics play a direct regulated role in gut microbiota. Interestingly, a present study suggested that polyphenols from green tea, oolong tea, and black tea could modulate the IM and generate short-chain fatty acids, and contribute to the improvements of human health.¹⁰⁰ There is evidence that the consumption of prebiotics may inhibit colorectal carcinogenesis in culture and animal models.^34,101–104 In healthy subjects, intervention trials indicated that palm, blackcurrant products, butyrylated starch, and wheat bran extract have a possible protective role in decreasing CRC risk.^105–108 In addition, prudent diet (rich in whole grains and dietary fiber) was related with a lower risk of F. nucleatum-positive CRCs, but not with negative ones, suggesting that the association of dietary patterns with CRC significantly differed by tissue F. nucleatum status.¹⁰⁹ By contrary, data from a Phase II chemoprevention trial did not provide convincing evidence of CRC risk reduction from 6-month interventions with pre-biotic dietary fiber.¹¹⁰ Currently, the clinical application of prebiotics in CRC treatment mainly focuses on combination with probiotics as synbiotics (Table 1), and the most of the outcomes are exciting and positive.

Noticeably, pre-/synbiotics therapies from clinical studies have not shown satisfactory results in all CRC population, which leads us to take into account its imperfect reasons. The human gut microbiome can be regarded as a “super organism” or “second genome” that regulates the host’s metabolism and immune system. So, does it also have positive and negative feedback regulation or self-regulation model similar to the human genome? If the answer is yes, then what is the molecular mechanism? In human genome, multiple genes and its related signaling exhibit a double effect in different human diseases; for example, c-Jun N-terminal kinase and p38α signaling pathways play a “good-cop and bad-cop” role in inflammatory and epigenetic modificatory diseases or tumorigenesis.^111,112 Interestingly, Lactobacillus gasseri could increase transforming growth factor (TGF)-β1 mRNA and protein secretion in colonic cell lines.¹¹³ It is well identified that TGF-β plays a contradictory role in premalignant and cancer cells, and the mechanism of gut microbiota affecting TGF-β levels in the development and progression of malignancies is still obscure. Such results invite the plausible hypothesis that 1) as a result of the different pathogenesis of inflammation, genetic mutations, and epigenetic modifications-associated CRC, whether pre-/synbiotics have dual function in these distinct patients; 2) there are some specific species in IM, maybe not pathogenic bacteria, which could also reduce/suppress the regulatory function of pre-/synbiotics, or even “kidnap” pre-/synbiotics and then participate in the procession of CRC under certain conditions; 3) although pre-/synbiotics do play an important role in modulation of immune development and function, and balance of IM, in some patients with severe gut microbiota dysbiosis may be beyond the control of prebiotics itself. If only these issues are fully investigated, can CRC be cured or controlled with simple daily use of pre-/synbiotics in the future.

Drugs intervention

Antibiotics are invaluable weapons to fight IBD, but long-term antibiotic use is associated with an increased risk of colorectal adenoma by altering the composition and functions of IM.¹¹⁴ It has been identified that gut microbiota is required for heme-induced epithelial hyperproliferation and hyperplasia because of the capacity to reduce mucus barrier function in colon.¹¹⁵ However, the suppression of microbiota by antibiotics was related to a reduction in crypt height and heme-induced colorectal carcinogenesis in rats.¹¹⁶ In addition, antibiotic drugs such as anisomycin, prodigiosin, and salinomycin had shown an inhibiting function in the growth of colorectal carcinoma cells by targeting different molecular mechanisms.^117–119 In inflammation-driven CRC mouse, targeted IM turned out an effective strategy for preventing the development of CRC under antibiotic treatment.³⁵ Interestingly, a study by Hamoya et al¹²⁰ suggested that erythromycin is useful as a chemopreventive agent and suppresses intestinal polyp development in mice, in part by attenuating local inflammation. Furthermore, treatment of mice bearing a colon cancer xenograft with the antibiotic metronidazole reduced Fusobacterium load, cancer cell proliferation, and overall tumor growth, which indicated antimicrobial interventions as a potential treatment for patients with Fusobacterium-associated CRC.¹²¹ Now, it is not clear whether these drugs found in natural microorganisms exert anti-CRC effects by affecting the function and balance of gut microbiota, but there is a viable way to explore and develop novel antibiotics or antibiotic peptides based on human IM itself. In the latest studies, the fingerprint of the human gastrointestinal (GI) tract microbiota aimed to study many complex bacterial ecosystems, which might push the development of narrow spectrum antibiotics and the application in CRC treatment, and formulate systems pharmacology and personalized therapeutics.^122,123

Moreover, a series of medications, including celecoxib, berberine, isoliquiritigenin, and curcumin, had been found to decrease the incidence of colorectal tumorigenesis by modulating the IM.^124–127 Another potential agent might be the herbal medicines, such as ginseng and astragalus, which are metabolized extensively by IM and could act as adjuvants for cancer chemoprevention.¹²⁸ Although these medicines are only used in mice models for this study, evidently it is feasible that the locus could be an attractive method for IM-based strategies.

FMT

FMT is a method of fecal suspension from healthy donors into the GI tract of individuals to cure specific diseases by reconstructing the normal function and the immune system of IM. As early as 1958, Eiseman et al¹²⁹ had first used FMT in mainstream medicine for the treatment of pseudomembra-nous colitis. In recent years, FMT is no longer considered an “alternative”, and is now gaining mainstream acceptance as a valuable biotherapeutic; although still poorly understood, it is used to treat GI diseases including IBD, Clostridium difficile infection, irritable bowel syndrome, and chronic constipation as well as a variety of non-GI disorders.^31,130 The transplants used in FMT could be either fresh stools or fecal frozen capsules, or extracts of bacterial flora from normal fecal flora.³¹ A recent study found that the FMT activated the tumor-associated Wnt/β-catenin signaling pathway, but microbiota depletion by a cocktail of antibiotics was sufficient to block deoxycholic acid-induced intestinal carcinogenesis in mice.¹³¹ Despite the evidence being lacking at present for FMT in CRC treatment, fecal microbiota from patients with CRC is identified to directly promote intestinal carcinogenesis in germ-free mice and mice given a carcinogen.²⁰ Thus, there is a reason to believe that FMT has a potential clinical effectiveness in the prevention and treatment of CRC by improving the balance and function of human IM.

It is notable that the impact of FMT on the recipient immune system is complicated and unpredictable, and the risk of dissemination of unknown pathogens through FMT cannot be eliminated.¹³² In addition, numerous outstanding questions remain, including FMT methodology – such as, what makes a “good donor,” routes of administration, preparation of transplant material, regulatory frameworks, and long-term effects of FMT.^31,133,134 If we can identify the favorable fecal microbiota composition or safe and functionally well-defined strains, and use prebiotics as the parcel material, FMT might be the low-burden alternative to chemo-/radiotherapy switch in the near future.

The roles of IM in other treatments

Surgery and chemo-/radiotherapy

Incorporation of pro-/synbiotic formulations in the preoperative mechanical bowel preparation is insufficient to be supported by the present evidence. Limited clinical trials could be promising in supporting their potential role in reducing postoperative infection and tumor recurrence, and promoting quality of life after CRC resection.^39,72 Chemo-/radiotherapy has become the most common method for advanced CRC patients, but the GI side-effect is a serious problem that increases the patient’s pain, and even endangers the patient’s life. Microbial β-glucuronidases in the intestines can reactivate the excreted, inactive metabolite of irinotecan, a first-line chemotherapeutic for metastatic CRC, which causes adverse drug responses, including severe diarrhea. A recent study applied an approach to cancer chemotherapy through the use of a high-turnover microbiota metabotype with potentially elevated levels for microbial β-glucuronidases, which indicated that inhibiting these enzymes may decrease irinotecan-dependent adverse drug responses in targeted subsets of CRC patients.¹³⁵ It is accepted that chemo-/radiotherapy-induced intestinal mucosal inflammation is closely related to the diversity of IM.¹³⁶ Meanwhile, gut microbiota had been found to affect host’s sensitivity to these therapies by modulating autophagy and metabolism.^{41,42,137,138} In addition, a mounting body of evidence had suggested that pro-/synbiotics could protect against chemo-/radiotherapy-induced diarrhea and mucosal inflammation.^75–77 Interestingly, Singh et al¹³⁹ developed an improved oral delivery system that comprises three components, namely nanoparticles of drug coated with natural materials such as prebiotics, and probiotics, which plays a dual role of protecting the drug in the gastric as well as intestinal conditions to allow its release only in the colon. Deciphering microbiome–host interactions before and after chemo-/radiotherapy may eventually allow prediction of CRC course and offer opportunities for the discovery of specific gut bacteria or metabolites as bioengineered adjuvant for chemo-/radiotherapy.

Immunotherapy

Tumor immunotherapy, a novel biotherapeutic, could stimulate and mobilize host’s immune system, and enhance anticancer immune response in tumor microenvironment, which eventually induces the apoptosis of carcinoma cells and inhibits tumor growth. However, the efficacy of immunotherapy has been a controversy in recent years. Negative regulation of tumor immune response is the most important reason to escape the antitumor immunotherapy mainly through recruiting or inducing inflammatory cells, including T regulatory cell (Treg), myeloid-derived suppressor cell (MDSC), and M2-like macrophage.¹⁴⁰ In addition, the immune-checkpoint proteins cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), programmed death-1 (PD-1), and programmed death receptor ligand-1 (PD-L1), and immunosuppressive cytokines of anticancer immune responses such as TGF-β, interleukin-10 (IL-10), IL-17, and IL-6, are also involved in the negative regulation of tumor immunity.^141–144 Notably, several reports have shown that gut microbiota is of great accommodative value to anticancer immunotherapy responses.^145–147

Treg cells could inhibit the function of CD4+ T cells, CD8+ T cells, dendritic cells (DC), and natural killer cells (NK), and promote the formation of immunosuppressive tumor microenvironment.¹⁴⁸ A recent study had found that the amplification of Treg cells was closely associated with the IM, ETBF-triggered chronic inflammation and colon tumorigenesis in mice through the enhancement of Treg proliferation and IL-17 production.¹⁴⁹ Importantly, cyclophosphamide (CTX) could induce the translocation of Gram-positive bacteria in the small intestine, provide “pathogenic” T helper 17 (pTh17) cells-based immune environment, and enhance the antitumor effect of CTX.¹⁵⁰ Additionally, Enterococcus hirae translocated from the small intestine to secondary lymphoid organs and increased the intratumoral CD8+/Treg ratio, and Barnesiella intestinihominis accumulated in the colon and promoted the infiltration of interferon-γ-producing γδT cells in cancer lesions, and in turn ameliorated the efficacy of anticancer immunomodulatory agent CTX.¹⁵¹ Moreover, CTX treatment decreased the proportion of Bacteroidetes while it increased the proportion of Firmicutes in the microbial community, and specific microbiota signatures belonging to Bacteroides and Alistipes respond to CTX therapy.¹⁵² Evidence of a pathogenic inflammatory signature in humans colonized with ETBF accelerated colorectal carcinogenesis, and promoted the differentiation of MDSCs, which selectively upregulated arginase-1 and nitric oxide synthase-2, produced NO, and suppressed T-cell proliferation.¹⁵³ Gram-negative strains such as Escherichia and Salmonella elevated inducible nitric oxide synthase expression,¹⁵⁴ and B. fragilis¹⁵⁵ also promoted the phagocytic functions of macrophages, polarizing them to an M1-like phenotype. IM imbalance can drive upregulation of IL-17C and B-cell lymphoma-2 in intestinal epithelial cells through TLR/MyD88-dependent signaling during intestinal tumorigenesis.¹⁵⁶ These studies support the notion that depressing negative regulator-associated inflammatory cells and immunosuppressive cytokines through improving IM may be an attractive and promising strategy for antitumor immunotherapy (Figure 1).

Figure 1.

The roles of intestinal microbiota in the regulation of tumor immunity.

Notes: Inflammatory cells including Treg, Th17, myeloid-derived suppressor cells, and M2 macrophage, immunosuppressive cytokines such as IL-17, IL-10, TGF-β, and IL-6, and immune-checkpoint proteins CTLA-4 and PD-1/PD-L1 are involved in the negative regulation of tumor immune response. It has shown that pathogenic bacteria (such as ETBF) or intestinal dysbacteriosis could drive amplification of inflammatory cells and upregulation of immunosuppressive cytokines through TLR-MyD88-dependent signaling. In addition, microbiota dysbiosis could inhibit the function of effector CD4+/CD8+ T cells, DC, and NK and promote the formation of immunosuppressive tumor microenvironment. By contrary, beneficial bacteria (such as Bacteroidales and Bifidobacterium) or microbiota eubiosis could favor the immune response of DC and T cells with anticancer properties through increasing the intratumoral effector CD4+/CD8+ proliferation and tumor necrosis factor, IL-2, IL-21, and IFN-γ production, which in turn inhibits the negative regulation of tumor immunity. Simultaneously holding immune-checkpoint antibody and probiotics could augment the function of DC and beneficial T cells, leading to enhanced CD8+ T-cell priming accumulation and sensitized CD28/B7 or blocked PD-1/PD-L1 axis in the tumor microenvironment.

Abbreviations: CTLA-4, cytotoxic T lymphocyte-associated antigen 4; DC, dentritic cells; EBTF, enterotoxigenic Bacteroides fragilis; IL, interleukin; NK, natural killer cells; PD-1, programmed death-1; PD-L1, programmed death receptor ligand-1; TGF, tumor growth factor.

Additional investigations had established that CD4+ CD25+ Treg cells could inhibit the immune function of activated T cells by upregulating the CTLA-4 expression,¹⁵⁷ which combines B7 on the antigen-presenting cell, and then antagonizes the activation of CD28/B7 signaling and the antitumor immune response.¹⁵⁸ Findings from animal tumor models and human studies, and simultaneous holding of anti-CTLA-4 antibody and Bacteroidales favored the immune response of DC and T cells with anticancer properties.³⁶ In addition, it had shown that increased representation of Bacteroidetes was correlated with resistance to the development of CTLA-4 blockade-induced colitis.¹⁵⁹ In addition to CTLA-4, another immune-checkpoint inhibitor, PD-1, could bind to tumor cell surface receptor PD-L1, sensitize PD-1/PD-L1 signaling pathway, and promote tumor cells to escape immune surveillance and killing.¹⁴¹ A new study claimed that enriched Clostridiales bacteria was found in responders’ gut microbiome undergoing anti-PD-1 immunotherapy in melanoma patients, and its underlying mechanism might be promoting the proliferation of beneficial T cells, and then inhibiting the level of immunosuppressive cells.¹⁶⁰ Oral administration of Bifidobacterium and PD-L1-specific antibody could augment DC function leading to enhance CD8+ T-cell priming accumulation in the tumor microenvironment, and then nearly abolish tumor outgrowth.¹⁶¹ Similar to these studies, Akkermansia muciniphila was identified to have a beneficial role in epithelial tumor patients who showed a good response to anti-PD-1 therapy, and oral supplementation with A. muciniphila post-FMT with nonresponder feces restored the efficacy of PD-1 blockade through increasing the recruitment of CCR9+ CXCR3+ CD4+ T cells into tumor beds.³⁷ Additionally, more abundant bacterial species was observed to have greater clinical response to immune-checkpoint inhibitor therapy, which suggested that the commensal microbiome may have a mechanistic impact on antitumor immunity in human cancer patients.^162,163 Besides these, commensal microbes combined with CpG oligo-nucleotide induced the release of TNF leading to antitumor immune response and tumor hemorrhagic necrosis through TRL4 signaling.¹⁶⁴ To this end, we summarized the regulated roles of anticancer immunotherapy using IM (Table 2) and explored its underlying mechanism in the regulation of tumor immune response (Figure 1).

Table 2.

The effects and mechanisms of intestinal microbiota in anticancer immunotherapy

Therapeutics	Regulation mechanism	Signatures	Reference
CTX	Stimulated memory Th1 immune responses, and provided “pathogenic” T helper 17 cells-based immune environment	Gram-positive bacteria	150
	Increased the intratumoral CD8+/Treg ratio, and promoted the infiltration of IFN-γ-producing γδT cells in cancer lesions	Enterococcus hirae and Barnesiella intestinihominis	151
CTLA-4 antibody	Favored the immune response of DC and T cells with anticancer properties	Bacteroidales	36
	Resisted to the development of checkpoint-blockade-induced colitis, reduced the risk of inflammatory complications	Bacteroidetes	36, 159
PD-1/PD-L1 antibody	Promoted the proliferation of beneficial T cells, and then inhibited the level of immunosuppressive cells	Clostridiales bacteria	160
	Augmented DC function leading to enhanced CD8+ T-cell priming accumulation in the tumor microenvironment	Bifidobacterium	161
	Increased the recruitment of CCR9+ CXCR3+ CD4+ T cells into tumor beds	Akkermansia muciniphila	37
CpG-ODN	Induced the release of tumor necrosis factor leading to anti-tumor immune response and tumor hemorrhagic necrosis through TRL4 signaling	Gram-negative Alistipes genera	164

Abbreviations: CCR9, CC chemokine receptor 9; CpG-ODN, CpG oligonucleotide; CTX, cyclophosphamide; CTLA-4, cytotoxic T-lymphocyte-associated antigen 4; CXCR3, C-X-C motif chemokine receptor 3; DC, dendritic cells; IFN, interferon; PD-1, programmed death 1; PD-L1, programmed death receptor ligand 1; TRL4, toll-like receptor 4.

Safety, deficiency, and future direction

Although studies of IM have just begun, gut microbiota-based CRC therapy is a comparatively safe method with less side effects that is easily accepted by patients. Because of individual heredity, dietary preference, and life habit, the prevention and curative effects of IM-based CRC treatment may also vary from each other. How to formulate reasonable prescriptions for different groups and races to prevent generating new IM disorders or derangements, especially when using FMT? Another concern relates to the long-term efficacy, novel administration routes, and new formulations, which also require a systematic and scientific evaluation approach.

Moreover, several important scientific problems remain to be addressed, such as follows: 1) For now, the classification of IM mostly depends on 16S rRNA sequencing, which is a relatively rough method that can distinguish family and genus of bacteria, but usually not species and strains. Therefore, a huge difference in the percentage of single bacteria may be omitted. DNA microarray,¹²² matrix-assisted laser desorption ionization time-of-flight mass spectrometry,¹⁶⁵ H-nuclear magnetic resonance spectroscopy,¹⁶⁶ as well as other newer methods might help to study many complex bacterial ecosystems and constitute personalized medicine for CRC patients. 2) Current data suggest that the association between Helicobacter pylori and colorectal neoplasms may be population dependent, indicating that certain CRC subtypes may also be infectious diseases.¹⁶⁷ The roles of gut microbiota in different CRC subtypes (including infection, inflammation, genetic mutations, and epigenetic modifications-associated CRC) are complex, and its maladjustment is the cause of tumorigenesis, or the result of tumor development is still uncertain. 3) Most studies on IM are based on animal models, especially the germ-free mice. Sterile mice are themselves a disease state; besides this, gut microbiota of humans and mice is also quite different, so using these animal studies to expand to clinical data needs to be carefully handled. 4) Despite that there are many clinical and preclinical tests about gut microbiota and CRC treatment, basically, a single or a few special bacterial communities are involved in these studies. The broad impact of commensal bacterial species on a wide range of health and/or CRC subjects will require consideration in settings of microorganism reconstitution with designer microbial syndicates, which is a commensal microbiome model including several gut strains. Notably, molecular pathologic epidemiology can enhance causal inference by linking putative etiology, and contribute to biomarker research and precision medicine. It can be used for research on dietary and environmental factors, microbiome, various omics, in combination with CRC phenotype including microbial profiling in tissues.^168,169

According to the data obtained over the past few years, it is plausible that gut microbiome could be used as an early diagnostic biomarker of CRC by using fecal proteomics and microbiota-based prediction, monitoring IM profile.^{165,170–172} In addition, checking specific biomarker of IM in urine has been predicted to reduce intestinal graft-versus-host disease and treatment-related mortality.¹⁷³ Gastric microbial composition can be used to distinguish chronic gastritis and gastric carcinoma.³² There is a reason to believe that CRC might be diagnosed in near future only through detecting characteristic markers of microbiota in feces, urine, or blood. Recent studies revealed that genetically modified bacteria as a tool to detect microscopic solid tumor masses even could effectively colonize solid tumors and act as antitumor therapeutics, suggesting that genetically manipulated bacteria has great potential in CRC treatment/prevention in the future.^174,175 Given the immunomodulatory effects and modern theories, gut microbiota can also be used to research CRC vaccines or adjuvant, which is applied for the maintainment of intestinal normal barrier and immune response. Moreover, IM might be used to monitor the sensitivity and outcomes of chemo-/radiotherapy and immunotherapy in CRC patients based on the recent studies in mice models. Besides these, immunotherapies or chemoimmunotherapies might also have variable reliance on gut microbiota for T-cell activation and function, and thus have a potential as novel strategies in individualized treatment.

Conclusion

Despite that there are still lots of deficiencies and problems associated with utilizing IM in CRC treatment, IM-based CRC therapy is well tolerant, comparatively safe, and of a comfortable pattern. Combined application of gut microbiota and other therapeutics, especially immunotherapy, shows a powerful synergistic efficiency to treat CRC settings or restrain side effect. Systematic and credible preclinical and clinical studies will help to get a good understanding of molecular mechanism, which could further expand the application of IM in the early diagnosis and prevention of CRC. We believe that it offers opportunities for the development of novel therapeutic or prophylactic strategies.