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The myeloid immune signature of enterotoxigenic Bacteroides fragilis-induced murine colon tumorigenesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/eji.200939892openalex-snapshot
Myeloid‐derived suppressor cells in inflammation: Uncovering cell subsets with enhanced immunosuppressive functions
inferredcites →https://doi.org/10.1002/eji.201142230openalex-snapshot
Tumor‐induced myeloid‐derived suppressor cell function is independent of IFN ‐γ and IL ‐4 R α
inferredcites →https://doi.org/10.1016/j.chom.2013.07.007openalex-snapshot
Fusobacterium nucleatum Potentiates Intestinal Tumorigenesis and Modulates the Tumor-Immune Microenvironment
inferredcites →https://doi.org/10.1016/j.chom.2014.02.007openalex-snapshot
Microbes, Microbiota, and Colon Cancer
inferredcites →https://doi.org/10.1016/j.immuni.2014.03.013openalex-snapshot
γδT17 Cells Promote the Accumulation and Expansion of Myeloid-Derived Suppressor Cells in Human Colorectal Cancer
inferredcites →https://doi.org/10.1038/nm.2015openalex-snapshot
A human colonic commensal promotes colon tumorigenesis via activation of T helper type 17 T cell responses
inferredcites →https://doi.org/10.1038/nm.3291openalex-snapshot
An interleukin-17–mediated paracrine network promotes tumor resistance to anti-angiogenic therapy
inferredcites →https://doi.org/10.1038/nri2506openalex-snapshot
Myeloid-derived suppressor cells as regulators of the immune system
inferredcites →https://doi.org/10.1038/nri3175openalex-snapshot
Coordinated regulation of myeloid cells by tumours
inferredcites →https://doi.org/10.1053/gast.2003.50047openalex-snapshot
Bacteroides fragilis enterotoxin induces c-Myc expression and cellular proliferation
inferredcites →https://doi.org/10.1073/pnas.1319051111openalex-snapshot
T helper 17 cells play a critical pathogenic role in lung cancer
inferredcites →https://doi.org/10.1084/jem.20090207openalex-snapshot
IL-17 can promote tumor growth through an IL-6–Stat3 signaling pathway
inferredcites →https://doi.org/10.1084/jem.20100587openalex-snapshot
HIF-1α regulates function and differentiation of myeloid-derived suppressor cells in the tumor microenvironment
inferredcites →https://doi.org/10.1084/jem.20140835openalex-snapshot
Immature myeloid cells directly contribute to skin tumor development by recruiting IL-17–producing CD4+ T cells
inferredcites →https://doi.org/10.1093/cid/ciu787openalex-snapshot
The Bacteroides fragilis Toxin Gene Is Prevalent in the Colon Mucosa of Colorectal Cancer Patients
inferredcites →https://doi.org/10.1093/infdis/jiw069openalex-snapshot
Reduction of Murine Colon Tumorigenesis Driven by EnterotoxigenicBacteroides fragilisUsing Cefoxitin Treatment
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a112652openalex-snapshot
DIET AND COLON CANCER
inferredcites →https://doi.org/10.1111/j.1469-0691.2006.01494.xopenalex-snapshot
A possible role of Bacteroides fragilis enterotoxin in the aetiology of colorectal cancer
inferredcites →https://doi.org/10.1111/j.1600-065x.2008.00610.xopenalex-snapshot
Indoleamine 2,3‐dioxygenase in T‐cell tolerance and tumoral immune escape
inferredcites →https://doi.org/10.1126/science.1224820openalex-snapshot
Intestinal Inflammation Targets Cancer-Inducing Activity of the Microbiota
inferredcites →https://doi.org/10.1126/scitranslmed.3007974openalex-snapshot
Disruption of CXCR2-Mediated MDSC Tumor Trafficking Enhances Anti-PD1 Efficacy
inferredcites →https://doi.org/10.1128/iai.72.10.5832-5839.2004openalex-snapshot
Bacteroides fragilis Enterotoxin Induces Intestinal Epithelial Cell Secretion of Interleukin-8 through Mitogen-Activated Protein Kinases and a Tyrosine Kinase-Regulated Nuclear Factor-κB Pathway
inferredcites →https://doi.org/10.1158/0008-5472.can-05-1299openalex-snapshot
Gr-1+CD115+ Immature Myeloid Suppressor Cells Mediate the Development of Tumor-Induced T Regulatory Cells and T-Cell Anergy in Tumor-Bearing Host
inferredcites →https://doi.org/10.1158/0008-5472.can-10-0775openalex-snapshot
IL-17 Enhances Tumor Development in Carcinogen-Induced Skin Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-10-2907openalex-snapshot
Clinical Impact of Different Classes of Infiltrating T Cytotoxic and Helper Cells (Th1, Th2, Treg, Th17) in Patients with Colorectal Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-13-2534openalex-snapshot
IL-17A Produced by γδ T Cells Promotes Tumor Growth in Hepatocellular Carcinoma
inferredcites →https://doi.org/10.1158/0008-5472.can-15-0749openalex-snapshot
Redundant Innate and Adaptive Sources of IL17 Production Drive Colon Tumorigenesis
inferredcites →https://doi.org/10.1158/2159-8290.cd-15-0447openalex-snapshot
Regulatory T-cell Response to Enterotoxigenic Bacteroides fragilis Colonization Triggers IL17-Dependent Colon Carcinogenesis
inferredcites →https://doi.org/10.1172/jci28828openalex-snapshot
Tumors induce a subset of inflammatory monocytes with immunosuppressive activity on CD8+ T cells
inferredcites →https://doi.org/10.1172/jci72334openalex-snapshot
Bacteroides fragilis subverts mucosal biology: from symbiont to colon carcinogenesis
inferredcites →https://doi.org/10.3201/eid0602.000210openalex-snapshot
Bacteroides fragilis Enterotoxin Gene Sequences in Patients with Inflammatory Bowel Disease
inferredcites →https://doi.org/10.4049/jimmunol.0802740openalex-snapshot
Myeloid-Derived Suppressor Cells: Linking Inflammation and Cancer
inferredcites →https://doi.org/10.4049/jimmunol.0902574openalex-snapshot
IL-17 Promotes Tumor Development through the Induction of Tumor Promoting Microenvironments at Tumor Sites and Myeloid-Derived Suppressor Cells
inferredcites →https://doi.org/10.4049/jimmunol.165.2.779openalex-snapshot
Gr-1+ Myeloid Cells Derived from Tumor-Bearing Mice Inhibit Primary T Cell Activation Induced Through CD3/CD28 Costimulation
inferredcites →https://doi.org/10.4049/jimmunol.181.7.4666openalex-snapshot
Proinflammatory S100 Proteins Regulate the Accumulation of Myeloid-Derived Suppressor Cells
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.chom.2018.01.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.clcc.2019.07.006openalex-snapshot
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Enterotoxigenic Bacteroides fragilis induces the stemness in colorectal cancer via upregulating histone demethylase JMJD2B
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Gut Microbiota in Tumor Microenvironment: A Critical Regulator in Cancer Initiation and Development as Potential Targets for Chinese Medicine
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The Four Horsemen in Colon Cancer
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Precancer Atlas to Drive Precision Prevention Trials
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Data from Bacterial-Driven Inflammation and Mutant BRAF Expression Combine to Promote Murine Colon Tumorigenesis That Is Sensitive to Immune Checkpoint Therapy
inferred← citeshttps://doi.org/10.1158/2159-8290.c.6549334.v1openalex-snapshot
Data from Bacterial-Driven Inflammation and Mutant BRAF Expression Combine to Promote Murine Colon Tumorigenesis That Is Sensitive to Immune Checkpoint Therapy
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-20-0770openalex-snapshot
Bacterial-Driven Inflammation and Mutant BRAF Expression Combine to Promote Murine Colon Tumorigenesis That Is Sensitive to Immune Checkpoint Therapy
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-21-1273openalex-snapshot
Human Colon Cancer–Derived Clostridioides difficile Strains Drive Colonic Tumorigenesis in Mice
inferred← citeshttps://doi.org/10.1159/000508328openalex-snapshot
Gut Microbiota Dysbiosis Drives the Development of Colorectal Cancer
inferred← citeshttps://doi.org/10.1172/jci155101openalex-snapshot
Colorectal cancer: the facts in the case of the microbiota
inferred← citeshttps://doi.org/10.1186/s12935-022-02554-6openalex-snapshot
Microbial and molecular differences according to the location of head and neck cancers
inferred← citeshttps://doi.org/10.1186/s12964-024-01615-9openalex-snapshot
Role of imbalanced gut microbiota in promoting CRC metastasis: from theory to clinical application
inferred← citeshttps://doi.org/10.1186/s13046-021-01983-xopenalex-snapshot
Gut microbiota-mediated immunomodulation in tumor
inferred← citeshttps://doi.org/10.1186/s13073-019-0621-2openalex-snapshot
Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
inferred← citeshttps://doi.org/10.1186/s13099-022-00489-xopenalex-snapshot
Enterotoxigenic Bacteroides fragilis activates IL-8 expression through Stat3 in colorectal cancer cells
inferred← citeshttps://doi.org/10.1186/s13099-025-00729-wopenalex-snapshot
Gut microbiome and gastric cancer: microbial interactions and therapeutic potential
inferred← citeshttps://doi.org/10.1186/s13099-025-00732-1openalex-snapshot
Phenotypic characterization and complete genome of a tumorigenic pathobiont Escherichia coli LI60C3
inferred← citeshttps://doi.org/10.1186/s40425-019-0757-zopenalex-snapshot
IL-17 inhibits CXCL9/10-mediated recruitment of CD8+ cytotoxic T cells and regulatory T cells to colorectal tumors
inferred← citeshttps://doi.org/10.1186/s40779-025-00623-1openalex-snapshot
Advancements in understanding tumor‑resident bacteria and their application in cancer therapy
inferred← citeshttps://doi.org/10.1186/s42047-026-00244-5openalex-snapshot
Cancer and the gut microbiome: the oncogenic impact of dysbiosis
inferred← citeshttps://doi.org/10.1186/s43556-023-00157-9openalex-snapshot
Mechanisms by which the intestinal microbiota affects gastrointestinal tumours and therapeutic effects
inferred← citeshttps://doi.org/10.1186/s43556-024-00200-3openalex-snapshot
Gut microbiome influences efficacy of Endostatin combined with PD-1 blockade against colorectal cancer
inferred← citeshttps://doi.org/10.1186/s43556-026-00512-6openalex-snapshot
Gut microbiota in health and disease
inferred← citeshttps://doi.org/10.1242/dmm.048793openalex-snapshot
It takes a village: microbiota, parainflammation, paligenosis and bystander effects in colorectal cancer initiation
inferred← citeshttps://doi.org/10.12677/acm.2025.15123583openalex-snapshot
The Role of Intestinal Microbiota Transplantation in the Prevention and Treatment of Colorectal Tumors and Related Research Advances
inferred← citeshttps://doi.org/10.1360/ssv-2025-0114openalex-snapshot
The function and mechanisms of gut microbiota in the treatment of colorectal cancer: from fundamental to clinical application
inferred← citeshttps://doi.org/10.1371/journal.pone.0297897openalex-snapshot
Keystone pathobionts associated with colorectal cancer promote oncogenic reprograming
inferred← citeshttps://doi.org/10.18297/etd/3013openalex-snapshot
Combination oral immunotherapy with IL-10 and IL-12 effectively treats colon tumors via synergistic effects on IL-17 producing T cells and colon epithelial barrier integrity.
inferred← citeshttps://doi.org/10.20524/aog.2020.0467openalex-snapshot
Understanding the microbiome: a primer on the role of the microbiome in colorectal neoplasia
inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2020.0476openalex-snapshot
Commensal microbiota in the digestive tract: a review of its roles in carcinogenesis and radiotherapy
inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2020.0651openalex-snapshot
Tumorigenic bacteria in colorectal cancer: mechanisms and treatments
inferred← citeshttps://doi.org/10.20892/j.issn.2095-3941.2023.0376openalex-snapshot
The role of intestinal flora on tumorigenesis, progression, and the efficacy of PD-1/PD-L1 antibodies in colorectal cancer
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1607997/v1openalex-snapshot
B. adolescentis Orchestrates CD143 + CAFs to Suppress Colorectal Tumorigenesis by Wnt signalling-regulated GAS1
inferred← citeshttps://doi.org/10.21203/rs.3.rs-29514/v1openalex-snapshot
WITHDRAWN: Fecal Enterotoxigenic Bacteroides fragilis-Peptostreptococcus stomatis-Parvimonas micra Biomarker for Noninvasive Diagnosis and Prognosis of Colorectal Laterally Spreading Tumor
inferred← citeshttps://doi.org/10.21315/mjms2020.27.4.2openalex-snapshot
The Mechanism of Bacteroides fragilis Toxin Contributes to Colon Cancer Formation
inferred← citeshttps://doi.org/10.2147/cmar.s153482openalex-snapshot
Role of intestinal flora in colorectal cancer from the metabolite perspective: a systematic review
inferred← citeshttps://doi.org/10.2147/cmar.s240108openalex-snapshot
Clinical Implications of the Associations Between Intestinal Microbiome and Colorectal Cancer Progression
inferred← citeshttps://doi.org/10.2147/ott.s170626openalex-snapshot
Intestinal microbiota: a novel perspective in colorectal cancer biotherapeutics
inferred← citeshttps://doi.org/10.2147/ott.s304298openalex-snapshot
Comprehensive Analysis of the Relationship Between Metabolic Reprogramming and Immune Function in Prostate Cancer
inferred← citeshttps://doi.org/10.2174/0113892010338997241216053634openalex-snapshot
Potential Pathogens Associated with Colorectal Cancer
inferred← citeshttps://doi.org/10.2174/1389201023666220307112413openalex-snapshot
Roles of Gut Microbiota in Colorectal Carcinogenesis Providing a Perspective for Early Diagnosis and Treatment
inferred← citeshttps://doi.org/10.2174/1574892816666210929164930openalex-snapshot
Advancement of Traditional Chinese Medicine in Regulation of Intestinal Flora: Mechanism-based Role in Disease Management
inferred← citeshttps://doi.org/10.21873/invivo.13327openalex-snapshot
Influence of the Oral Health Assessment Tool Score on Survival of Patients With Esophageal Cancer
inferred← citeshttps://doi.org/10.2217/fon-2018-0595openalex-snapshot
Relationship Between Intestinal Microorganisms and T Lymphocytes In Colorectal Cancer
inferred← citeshttps://doi.org/10.3389/fcell.2021.725821openalex-snapshot
Dietary Patterns and Associated Microbiome Changes that Promote Oncogenesis
inferred← citeshttps://doi.org/10.3389/fcell.2021.732192openalex-snapshot
Toll Like Receptors as Sensors of the Tumor Microbial Dysbiosis: Implications in Cancer Progression
inferred← citeshttps://doi.org/10.3389/fcimb.2020.572570openalex-snapshot
Microbes in Tumoral In Situ Tissues and in Tumorigenesis
inferred← citeshttps://doi.org/10.3389/fcimb.2022.906719openalex-snapshot
Editorial: “The Host-Microbiome Interplay in Colorectal Cancer”
inferred← citeshttps://doi.org/10.3389/fcimb.2022.953718openalex-snapshot
The interplay between Helicobacter pylori and the gut microbiota: An emerging driver influencing the immune system homeostasis and gastric carcinogenesis
inferred← citeshttps://doi.org/10.3389/fcimb.2026.1858868openalex-snapshot
Virulome over taxonomy: refining the driver-passenger model in colorectal carcinogenesis
inferred← citeshttps://doi.org/10.3389/fendo.2024.1355387openalex-snapshot
Systematic review on the role of the gut microbiota in tumors and their treatment
inferred← citeshttps://doi.org/10.3389/fimmu.2017.01895openalex-snapshot
Monocytic Myeloid-Derived Suppressor Cells in Chronic Infections
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00946openalex-snapshot
Concepts Collide: Genomic, Immune, and Microbial Influences on the Tumor Microenvironment and Response to Cancer Therapy
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1032294openalex-snapshot
Stress and cancer: The mechanisms of immune dysregulation and management
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1087755openalex-snapshot
The effects of traditional Chinese medicine and dietary compounds on digestive cancer immunotherapy and gut microbiota modulation: A review
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1349067openalex-snapshot
Modulation of myeloid-derived suppressor cell functions by oral inflammatory diseases and important oral pathogens
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1535955openalex-snapshot
Nervous system–gut microbiota–immune system axis: future directions for preventing tumor
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1642091openalex-snapshot
Tumor-associated macrophages in colon cancer immunotherapy: mechanisms, natural product interventions, and microenvironment remodeling
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1700487openalex-snapshot
NOS2/ARG1 axis and immune cell ratios as promising prognostic and predictive biomarkers for Cetuximab combined with chemotherapy in wt-KRAS human colorectal cancer
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1768792openalex-snapshot
The microbiota–metabolite–immune axis in colorectal cancer: mechanistic insights and emerging clinical applications
inferred← citeshttps://doi.org/10.3389/fmicb.2018.01835openalex-snapshot
The Human Gut Microbiome – A Potential Controller of Wellness and Disease
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1125195openalex-snapshot
House ammonia exposure causes alterations in microbiota, transcriptome, and metabolome of rabbits
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1462749openalex-snapshot
From pathogenesis to treatment: the impact of bacteria on cancer
inferred← citeshttps://doi.org/10.3389/fmolb.2023.1140325openalex-snapshot
Interaction of gut microbiota with the tumor microenvironment: A new strategy for antitumor treatment and traditional Chinese medicine in colorectal cancer
inferred← citeshttps://doi.org/10.3389/fonc.2021.661048openalex-snapshot
Fecal Enterotoxigenic Bacteroides fragilis–Peptostreptococcus stomatis–Parvimonas micra Biomarker for Noninvasive Diagnosis and Prognosis of Colorectal Laterally Spreading Tumor
inferred← citeshttps://doi.org/10.3389/fonc.2022.781233openalex-snapshot
Functional and Therapeutic Significance of Tumor-Associated Macrophages in Colorectal Cancer
inferred← citeshttps://doi.org/10.3389/fonc.2023.1344328openalex-snapshot
The role of microbiomes in gastrointestinal cancers: new insights
inferred← citeshttps://doi.org/10.3389/fphar.2022.964793openalex-snapshot
New insights into natural products that target the gut microbiota: Effects on the prevention and treatment of colorectal cancer
inferred← citeshttps://doi.org/10.3389/fphar.2023.1208044openalex-snapshot
The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
inferred← citeshttps://doi.org/10.3390/biomedicines12122776openalex-snapshot
Microbiota and Cytokine Modulation: Innovations in Enhancing Anticancer Immunity and Personalized Cancer Therapies
inferred← citeshttps://doi.org/10.3390/cancers13164054openalex-snapshot
Microbiota-Associated Metabolites and Related Immunoregulation in Colorectal Cancer
inferred← citeshttps://doi.org/10.3390/cancers14041019openalex-snapshot
Bacterial Involvement in Progression and Metastasis of Colorectal Neoplasia
inferred← citeshttps://doi.org/10.3390/cancers14153563openalex-snapshot
The Effect of the Gut Microbiota on Systemic and Anti-Tumor Immunity and Response to Systemic Therapy against Cancer
inferred← citeshttps://doi.org/10.3390/cancers15030866openalex-snapshot
Gut Microbiota in Colorectal Cancer: Biological Role and Therapeutic Opportunities
inferred← citeshttps://doi.org/10.3390/cells11223684openalex-snapshot
The Species of Gut Bacteria Associated with Antitumor Immunity in Cancer Therapy
inferred← citeshttps://doi.org/10.3390/cimb47020106openalex-snapshot
Advancements in the Pathogenesis, Diagnosis, and Therapeutic Implications of Intestinal Bacteria
inferred← citeshttps://doi.org/10.3390/diagnostics16111582openalex-snapshot
Microbiomics: Novel Biomarkers of Colorectal Cancer Diagnosis and Prognosis
inferred← citeshttps://doi.org/10.3390/ijms20184560openalex-snapshot
Zerumbone Suppresses Enterotoxigenic Bacteroides fragilis Infection-Induced Colonic Inflammation through Inhibition of NF-κΒ
inferred← citeshttps://doi.org/10.3390/ijms21176201openalex-snapshot
Gut Microbiota and Colon Cancer: A Role for Bacterial Protein Toxins?
inferred← citeshttps://doi.org/10.3390/ijms21176207openalex-snapshot
Involvement of Fusobacterium Species in Oral Cancer Progression: A Literature Review Including Other Types of Cancer
inferred← citeshttps://doi.org/10.3390/ijms21218034openalex-snapshot
Dietary Salt Administration Decreases Enterotoxigenic Bacteroides fragilis (ETBF)-Promoted Tumorigenesis via Inhibition of Colonic Inflammation
inferred← citeshttps://doi.org/10.3390/ijms24044060openalex-snapshot
The Anti-Tumorigenic Role of Cannabinoid Receptor 2 in Colon Cancer: A Study in Mice and Humans
inferred← citeshttps://doi.org/10.3390/ijms25010364openalex-snapshot
Promotion of Colitis in B Cell-Deficient C57BL/6 Mice Infected with Enterotoxigenic Bacteroides fragilis
inferred← citeshttps://doi.org/10.3390/ijms252413308openalex-snapshot
Study of Microbiota Associated to Early Tumors Can Shed Light on Colon Carcinogenesis
inferred← citeshttps://doi.org/10.3390/ijms26104818openalex-snapshot
Microbiome Markers in Gastrointestinal Disorders: Inflammatory Bowel Disease, Colorectal Cancer, and Celiac Disease
inferred← citeshttps://doi.org/10.3390/ijms26136218openalex-snapshot
Modeling ETBF-Mediated Colorectal Tumorigenesis Using AOM/DSS in Wild-Type Mice
inferred← citeshttps://doi.org/10.3390/jcm8101669openalex-snapshot
Chronic Stress, Inflammation, and Colon Cancer: A CRH System-Driven Molecular Crosstalk
inferred← citeshttps://doi.org/10.3390/medsci14060669openalex-snapshot
From Dysbiosis to Symbiosis: Using the Gut Microbiome to Improve Cancer Outcomes
inferred← citeshttps://doi.org/10.3390/microorganisms10112129openalex-snapshot
Host Genetics and Microbiota Interactions in Colorectal Cancer: Shared or Independent Risk?
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