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Bacteroides fragilis subverts mucosal biology: from symbiont to colon carcinogenesis
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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.200526321openalex-snapshot
Mitogen‐activated protein kinase and activator protein‐1 dependent signals are essential for Bacteroides fragilis enterotoxin‐induced enteritis
inferredcites →https://doi.org/10.1002/eji.200535808openalex-snapshot
Bacteroides fragilisenterotoxin induces cyclooxygenase‐2 and fluid secretion in intestinal epithelial cells through NF‐κB activation
inferredcites →https://doi.org/10.1002/eji.200838191openalex-snapshot
Inhibition of apoptosis in Bacteroides fragilis enterotoxin‐stimulated intestinal epithelial cells through the induction of c‐IAP‐2
inferredcites →https://doi.org/10.1002/ibd.20265openalex-snapshot
Enterotoxigenic Bacteroides fragilis: A potential instigator of colitis
inferredcites →https://doi.org/10.1016/j.cell.2005.05.007openalex-snapshot
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
inferredcites →https://doi.org/10.1016/j.cellsig.2009.01.006openalex-snapshot
The role of cell adhesion molecules in the progression of colorectal cancer and the development of liver metastasis
inferredcites →https://doi.org/10.1016/j.chom.2012.08.004openalex-snapshot
Outer Membrane Vesicles of a Human Commensal Mediate Immune Regulation and Disease Protection
inferredcites →https://doi.org/10.1016/j.chom.2014.02.007openalex-snapshot
Microbes, Microbiota, and Colon Cancer
inferredcites →https://doi.org/10.1023/b:ddas.0000042241.13489.88openalex-snapshot
Are Helicobacter Species and Enterotoxigenic Bacteroides fragilis Involved in Inflammatory Bowel Disease?
inferredcites →https://doi.org/10.1038/35107092openalex-snapshot
Extensive surface diversity of a commensal microorganism by multiple DNA inversions
inferredcites →https://doi.org/10.1038/nature02285openalex-snapshot
The strict anaerobe Bacteroides fragilis grows in and benefits from nanomolar concentrations of oxygen
inferredcites →https://doi.org/10.1038/nature07008openalex-snapshot
A microbial symbiosis factor prevents intestinal inflammatory disease
inferredcites →https://doi.org/10.1038/nature11234openalex-snapshot
Structure, function and diversity of the healthy human microbiome
inferredcites →https://doi.org/10.1038/nature11412openalex-snapshot
Comprehensive molecular portraits of human breast tumours
inferredcites →https://doi.org/10.1038/nature11465openalex-snapshot
Adenoma-linked barrier defects and microbial products drive IL-23/IL-17-mediated tumour growth
inferredcites →https://doi.org/10.1038/nature12447openalex-snapshot
Bacterial colonization factors control specificity and stability of the gut microbiota
inferredcites →https://doi.org/10.1038/ni.2060openalex-snapshot
Inflammation meets cancer, with NF-κB as the matchmaker
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/10.1046/j.1365-2249.2002.01921.xopenalex-snapshot
Nuclear factor-kappa B activation pathway in intestinal epithelial cells is a major regulator of chemokine gene expression and neutrophil migration induced byBacteroides fragilisenterotoxin
inferredcites →https://doi.org/10.1053/gast.2003.50047openalex-snapshot
Bacteroides fragilis enterotoxin induces c-Myc expression and cellular proliferation
inferredcites →https://doi.org/10.1053/j.gastro.2011.01.057openalex-snapshot
Intestinal Inflammation and Cancer
inferredcites →https://doi.org/10.1056/nejmoa1109400openalex-snapshot
Intestinal Microbial Metabolism of Phosphatidylcholine and Cardiovascular Risk
inferredcites →https://doi.org/10.1073/pnas.0909122107openalex-snapshot
Inducible Foxp3 + regulatory T-cell development by a commensal bacterium of the intestinal microbiota
inferredcites →https://doi.org/10.1073/pnas.1010203108openalex-snapshot
Polyamine catabolism contributes to enterotoxigenic Bacteroides fragilis -induced colon tumorigenesis
inferredcites →https://doi.org/10.1073/pnas.95.25.14979openalex-snapshot
Bacteroides fragilis enterotoxin cleaves the zonula adherens protein, E-cadherin
inferredcites →https://doi.org/10.1086/591130openalex-snapshot
Association of EnterotoxigenicBacteroides fragilisInfection with Inflammatory Diarrhea
inferredcites →https://doi.org/10.1086/598639openalex-snapshot
Prevalence of Enterotoxigenic Bacteroides fragilis in Adult Patients with Diarrhea and Healthy Controls
inferredcites →https://doi.org/10.1093/carcin/20.8.1425openalex-snapshot
Increased tight junctional permeability is associated with the development of colon cancer
inferredcites →https://doi.org/10.1093/infdis/136.1.82openalex-snapshot
The Capsular Polysaccharide of Bacteroides fragilis as a Virulence Factor: Comparison of the Pathogenic Potential of Encapsulated and Unencapsulated Strains
inferredcites →https://doi.org/10.1093/infdis/140.5.724openalex-snapshot
Protective Efficacy of Immunization with Capsular Antigen against Experimental Infection with Bacteroides fragilis
inferredcites →https://doi.org/10.1093/jinfdis/jiq061openalex-snapshot
Perspective: Alpha-Bugs, Their Microbial Partners, and the Link to Colon Cancer
inferredcites →https://doi.org/10.1097/mib.0000000000000019openalex-snapshot
Stat3 Activation in Murine Colitis Induced by Enterotoxigenic Bacteroides fragilis
inferredcites →https://doi.org/10.1097/mib.0b013e318297d884openalex-snapshot
Relevance of Commensal Microbiota in the Treatment and Prevention of Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1099/00222615-29-3-171openalex-snapshot
Epidemiology of the Bacteroides fragilis group in the colonic flora in 10 patients with colonic 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/10.1126/science.1094291openalex-snapshot
Convergence of Wnt, ß-Catenin, and Cadherin Pathways
inferredcites →https://doi.org/10.1126/science.1106469openalex-snapshot
Human Symbionts Use a Host-Like Pathway for Surface Fucosylation
inferredcites →https://doi.org/10.1126/science.1241214openalex-snapshot
Gut Microbiota from Twins Discordant for Obesity Modulate Metabolism in Mice
inferredcites →https://doi.org/10.1126/science.275.5307.1787openalex-snapshot
Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC
inferredcites →https://doi.org/10.1126/science.281.5382.1509openalex-snapshot
Identification of c- MYC as a Target of the APC Pathway
inferredcites →https://doi.org/10.1126/science.8211161openalex-snapshot
Structural Features of Polysaccharides That Induce Intra-Abdominal Abscesses
inferredcites →https://doi.org/10.1128/cmr.00053-08openalex-snapshot
Enterotoxigenic Bacteroides fragilis : a Rogue among Symbiotes
inferredcites →https://doi.org/10.1128/iai.00060-06openalex-snapshot
The Bacteroides fragilis Toxin Binds to a Specific Intestinal Epithelial Cell Receptor
inferredcites →https://doi.org/10.1128/iai.00814-08openalex-snapshot
Induction of Persistent Colitis by a Human Commensal, EnterotoxigenicBacteroides fragilis, in Wild-Type C57BL/6 Mice
inferredcites →https://doi.org/10.1128/iai.01348-10openalex-snapshot
Longitudinal Analysis of the Prevalence, Maintenance, and IgA Response to Species of the Order Bacteroidales in the Human Gut
inferredcites →https://doi.org/10.1128/iai.44.2.241-244.1984openalex-snapshot
Bacteroides fragilis: a possible cause of acute diarrheal disease in newborn lambs
inferredcites →https://doi.org/10.1128/iai.63.1.175-181.1995openalex-snapshot
The enterotoxin of Bacteroides fragilis is a metalloprotease
inferredcites →https://doi.org/10.1128/iai.63.10.3820-3826.1995openalex-snapshot
Proteolytic activity of the Bacteroides fragilis enterotoxin causes fluid secretion and intestinal damage in vivo
inferredcites →https://doi.org/10.1128/iai.64.11.4480-4487.1996openalex-snapshot
Attachment of a noninvasive enteric pathogen, enteropathogenic Escherichia coli, to cultured human intestinal epithelial monolayers induces transmigration of neutrophils
inferredcites →https://doi.org/10.1128/iai.64.12.5029-5034.1996openalex-snapshot
Bacteroides fragilis toxin rapidly intoxicates human intestinal epithelial cells (HT29/C1) in vitro
inferredcites →https://doi.org/10.1128/iai.65.4.1431-1439.1997openalex-snapshot
The Bacteroides fragilis toxin fragilysin disrupts the paracellular barrier of epithelial cells
inferredcites →https://doi.org/10.1128/iai.65.9.3561-3570.1997openalex-snapshot
Bacteroides fragilis toxin exhibits polar activity on monolayers of human intestinal epithelial cells (T84 cells) in vitro
inferredcites →https://doi.org/10.1128/iai.66.4.1735-1739.1998openalex-snapshot
Molecular Characterization of the Fragilysin Pathogenicity Islet of Enterotoxigenic Bacteroides fragilis
inferredcites →https://doi.org/10.1128/iai.67.9.4945-4949.1999openalex-snapshot
Identification of a Third Metalloprotease Toxin Gene in Extraintestinal Isolates of Bacteroides fragilis
inferredcites →https://doi.org/10.1128/iai.70.5.2463-2471.2002openalex-snapshot
Diversity of the Metalloprotease Toxin Produced by Enterotoxigenic Bacteroides fragilis
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/10.1128/jcm.21.3.472-473.1985openalex-snapshot
Isolation of Bacteroides fragilis from the feces of diarrheic calves and lambs
inferredcites →https://doi.org/10.1128/jcm.25.12.2330-2333.1987openalex-snapshot
Isolation of enterotoxigenic Bacteroides fragilis from humans with diarrhea
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-12-4607openalex-snapshot
Understanding Phenotypic Variation in Rodent Models with Germline Apc Mutations
inferredcites →https://doi.org/10.1177/104063878900100413openalex-snapshot
Exfoliating Colitis Associated with Enterotoxigenic Bacteroides Fragilis in a Piglet
inferredcites →https://doi.org/10.1242/jcs.03455openalex-snapshot
Bacteroides fragilis toxin stimulates intestinal epithelial cell shedding and γ-secretase-dependent E-cadherin cleavage
inferredcites →https://doi.org/10.1371/journal.pone.0039743openalex-snapshot
Human Intestinal Lumen and Mucosa-Associated Microbiota in Patients with Colorectal Cancer
inferredcites →https://doi.org/10.2460/ajvr.1987.48.11.1565openalex-snapshot
Diarrhea associated with enterotoxigenic Bacteroides fragilis in foals
inferredcites →https://doi.org/10.3201/eid0602.000210openalex-snapshot
Bacteroides fragilis Enterotoxin Gene Sequences in Patients with Inflammatory Bowel Disease
inferredcites →https://doi.org/10.7326/0003-4819-86-5-569openalex-snapshot
Bacteroides fragilis Subspecies in Clinical Isolates
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Breaking resistance: in silico subtractive and comparative genomics approaches for drug targeting in Bacteroides fragilis
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To resist and persist: Important factors in the pathogenesis of Bacteroides fragilis
inferred← citeshttps://doi.org/10.1016/j.molmed.2015.02.006openalex-snapshot
Autoimmune host–microbiota interactions at barrier sites and beyond
inferred← citeshttps://doi.org/10.1016/j.semcancer.2022.07.006openalex-snapshot
Microbiota and lung cancer
inferred← citeshttps://doi.org/10.1016/j.tim.2016.02.010openalex-snapshot
Dancing with the Stars: How Choreographed Bacterial Interactions Dictate Nososymbiocity and Give Rise to Keystone Pathogens, Accessory Pathogens, and Pathobionts
inferred← citeshttps://doi.org/10.1016/j.trecan.2019.12.007openalex-snapshot
The Influence of Lung Microbiota on Lung Carcinogenesis, Immunity, and Immunotherapy
inferred← citeshttps://doi.org/10.1017/s0007114519000011openalex-snapshot
Maternal dyslipidaemic diet induces sex-specific alterations in intestinal function and lipid metabolism in rat offspring
inferred← citeshttps://doi.org/10.1021/acsestwater.3c00016openalex-snapshot
Differential Characteristics of Waterborne Bacterial Pathogens and Virulence Factors between Suspended Particulate Matters and Aqueous Phase in the Pearl River and Pearl River Estuary
inferred← citeshttps://doi.org/10.1038/mi.2016.53openalex-snapshot
The myeloid immune signature of enterotoxigenic Bacteroides fragilis-induced murine colon tumorigenesis
inferred← citeshttps://doi.org/10.1038/nrmicro.2016.171openalex-snapshot
Collateral damage: insights into bacterial mechanisms that predispose host cells to cancer
inferred← citeshttps://doi.org/10.1038/s12276-019-0313-4openalex-snapshot
Development of a colorectal cancer diagnostic model and dietary risk assessment through gut microbiome analysis
inferred← citeshttps://doi.org/10.1038/s41366-021-00866-7openalex-snapshot
Spot-light on microbiota in obesity and cancer
inferred← citeshttps://doi.org/10.1038/s41417-024-00862-9openalex-snapshot
LRP11-AS1 mediates enterotoxigenic Bacteroides fragilis-related carcinogenesis in colorectal Cancer via the miR-149-3p/CDK4 pathway
inferred← citeshttps://doi.org/10.1038/s41419-019-1925-2openalex-snapshot
Long noncoding RNA BFAL1 mediates enterotoxigenic Bacteroides fragilis-related carcinogenesis in colorectal cancer via the RHEB/mTOR pathway
inferred← citeshttps://doi.org/10.1038/s41467-020-15342-5openalex-snapshot
Colonic microbiota is associated with inflammation and host epigenomic alterations in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1038/s41467-024-48662-xopenalex-snapshot
Long-term relapse-free survival enabled by integrating targeted antibacteria in antitumor treatment
inferred← citeshttps://doi.org/10.1038/s41522-017-0040-3openalex-snapshot
High-resolution bacterial 16S rRNA gene profile meta-analysis and biofilm status reveal common colorectal cancer consortia
inferred← citeshttps://doi.org/10.1038/s41564-023-01559-9openalex-snapshot
Bacteroides fragilis toxin expression enables lamina propria niche acquisition in the developing mouse gut
inferred← citeshttps://doi.org/10.1038/s41564-023-01569-7openalex-snapshot
Bacteroides fragilis uses toxins for gut success
inferred← citeshttps://doi.org/10.1038/s41564-024-01736-4openalex-snapshot
Interactions between diet and gut microbiota in cancer
inferred← citeshttps://doi.org/10.1038/s41568-023-00594-2openalex-snapshot
Bacteria in cancer initiation, promotion and progression
inferred← citeshttps://doi.org/10.1038/s41575-019-0209-8openalex-snapshot
Gut microbiota in colorectal cancer: mechanisms of action and clinical applications
inferred← citeshttps://doi.org/10.1038/s41598-017-05264-6openalex-snapshot
Outer membrane vesicles secreted by pathogenic and nonpathogenic Bacteroides fragilis represent different metabolic activities
inferred← citeshttps://doi.org/10.1038/s41598-019-55613-wopenalex-snapshot
Designing a multi-epitopic vaccine against the enterotoxigenic Bacteroides fragilis based on immunoinformatics approach
inferred← citeshttps://doi.org/10.1038/s41598-020-67843-4openalex-snapshot
The colonic mucosa-associated microbiome in SIV infection: shift towards Bacteroidetes coincides with mucosal CD4+ T cell depletion and enterocyte damage
inferred← citeshttps://doi.org/10.1038/s41598-023-42481-8openalex-snapshot
Protective effects of a new generation of probiotic Bacteroides fragilis against colitis in vivo and in vitro
inferred← citeshttps://doi.org/10.1038/s41598-025-20976-wopenalex-snapshot
The impact of Streptococcus thermophilus IDCC 2201 on gut microbiota and its potential as a prophylactic agent for colorectal cancer
inferred← citeshttps://doi.org/10.1038/s42003-021-02014-3openalex-snapshot
G-protein coupled receptor 35 (GPR35) regulates the colonic epithelial cell response to enterotoxigenic Bacteroides fragilis
inferred← citeshttps://doi.org/10.1039/9781788016506-00261openalex-snapshot
Nutrition, the Gastrointestinal Microbiota and Cancer Prevention
inferred← citeshttps://doi.org/10.1039/d3mo00021dopenalex-snapshot
Meta-analyses of host metagenomes from colorectal cancer patients reveal strong relationship between colorectal cancer-associated species
inferred← citeshttps://doi.org/10.1039/d5sc09900eopenalex-snapshot
The hidden language of gut-derived lipopolysaccharides: fine chemistry, huge immunological consequences
inferred← citeshttps://doi.org/10.1053/j.gastro.2017.10.030openalex-snapshot
Human Intestinal Microbiota and Colorectal Cancer: Moving Beyond Associative Studies
inferred← citeshttps://doi.org/10.1053/j.gastro.2018.10.011openalex-snapshot
The Unfolding Story of ATF6, Microbial Dysbiosis, and Colorectal Cancer
inferred← citeshttps://doi.org/10.1053/j.gastro.2021.08.003openalex-snapshot
Enterotoxigenic Bacteroides fragilis Promotes Intestinal Inflammation and Malignancy by Inhibiting Exosome-Packaged miR-149-3p
inferred← citeshttps://doi.org/10.1053/j.scrs.2017.09.003openalex-snapshot
How the microbiome is shaping our understanding of cancer biology and its treatment
inferred← citeshttps://doi.org/10.1053/j.seminoncol.2015.09.001openalex-snapshot
The microbiome and its potential as a cancer preventive intervention
inferred← citeshttps://doi.org/10.1055/a-2435-2659openalex-snapshot
Effect of Bacteroides on Crohn’s disease
inferred← citeshttps://doi.org/10.1074/jbc.tm118.003337openalex-snapshot
Polyamine catabolism and oxidative damage
inferred← citeshttps://doi.org/10.1080/19490976.2016.1150414openalex-snapshot
Taurocholic acid metabolism by gut microbes and colon cancer
inferred← citeshttps://doi.org/10.1080/19490976.2016.1155020openalex-snapshot
Targeting colorectal cancer-associated bacteria: A new area of research for personalized treatments
inferred← citeshttps://doi.org/10.1080/19490976.2020.1788900openalex-snapshot
Enterotoxigenic Bacteroides fragilis induces the stemness in colorectal cancer via upregulating histone demethylase JMJD2B
inferred← citeshttps://doi.org/10.1080/19490976.2026.2664684openalex-snapshot
Gut microbiota and diet in colorectal cancer: Converging determinants of carcinogenesis
inferred← citeshttps://doi.org/10.1080/2162402x.2015.1118601openalex-snapshot
Procarcinogenic regulatory T cells in microbial-induced colon cancer
inferred← citeshttps://doi.org/10.1080/2162402x.2020.1868122openalex-snapshot
Oral administration of Bifidobacterium breve promotes antitumor efficacy via dendritic cells-derived interleukin 12
inferred← citeshttps://doi.org/10.1093/ecco-jcc/jjae179openalex-snapshot
Bacteroides fragilis Toxin Suppresses METTL3-Mediated m6A Modification in Macrophage to Promote Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1093/ecco-jcc/jjag099openalex-snapshot
Rapid resolution of colon inflammation and microbiome remodeling with vancomycin therapy in a patient with primary sclerosing cholangitis
inferred← citeshttps://doi.org/10.1093/femsml/uqaf039openalex-snapshot
Exploring Bacteroidota strains from human stool and animal feces: phenotyping and functional diversity
inferred← citeshttps://doi.org/10.1093/femspd/ftv105openalex-snapshot
Bacterial protein toxins in human cancers
inferred← citeshttps://doi.org/10.1093/gastro/gox031openalex-snapshot
Dysbiosis of gut microbiota in promoting the development of colorectal cancer
inferred← citeshttps://doi.org/10.1093/gigascience/giy121openalex-snapshot
MetaPGN: a pipeline for construction and graphical visualization of annotated pangenome networks
inferred← citeshttps://doi.org/10.1093/ibd/izab291openalex-snapshot
Bringing to Light the Risk of Colorectal Cancer in Inflammatory Bowel Disease: Mucosal Glycosylation as a Key Player
inferred← citeshttps://doi.org/10.1093/infdis/jiw069openalex-snapshot
Reduction of Murine Colon Tumorigenesis Driven by EnterotoxigenicBacteroides fragilisUsing Cefoxitin Treatment
inferred← citeshttps://doi.org/10.1093/procel/pwae067openalex-snapshot
Oncomicrobial vaccines mitigate tumor progression via precisely targeting oncomicrobes in mice
inferred← citeshttps://doi.org/10.1097/cm9.0000000000003617openalex-snapshot
Intestinal dysbiosis and colorectal cancer
inferred← citeshttps://doi.org/10.1097/qco.0000000000000196openalex-snapshot
The intestinal microbiome and health
inferred← citeshttps://doi.org/10.1099/jmm.0.001903openalex-snapshot
Robust prediction of colorectal cancer via gut microbiome 16S rRNA sequencing data
inferred← citeshttps://doi.org/10.1099/mic.0.000565openalex-snapshot
Complementation of a metK-deficient E. coli strain with heterologous AdoMet synthetase genes
inferred← citeshttps://doi.org/10.1101/2024.12.18.628894openalex-snapshot
Exploring new Bacteroidota strains: Functional Diversity and Probiotic Characteristics
inferred← citeshttps://doi.org/10.1101/273524openalex-snapshot
Microbiome-TP53 Gene Interaction in Human Lung Cancer
inferred← citeshttps://doi.org/10.1111/1750-3841.16772openalex-snapshot
The preventive effects of inulin, cellulose, and their mixture on colorectal cancer liver metastasis in mice by regulating gut microbiota
inferred← citeshttps://doi.org/10.1111/1753-0407.13593openalex-snapshot
Probiotic treatment with viable α‐galactosylceramide ‐producing Bacteroides fragilis reduces diabetes incidence in female nonobese diabetic mice
inferred← citeshttps://doi.org/10.1111/bjh.18574openalex-snapshot
Prolonged gut microbial alterations in post‐transplant survivors of allogeneic haematopoietic stem cell transplantation
inferred← citeshttps://doi.org/10.1111/dom.16129openalex-snapshot
The impact of novel probiotics isolated from the human gut on the gut microbiota and health
inferred← citeshttps://doi.org/10.1111/jgh.14516openalex-snapshot
Single probiotic supplement suppresses colitis‐associated colorectal tumorigenesis by modulating inflammatory development and microbial homeostasis
inferred← citeshttps://doi.org/10.1111/jgh.15716openalex-snapshot
What is unknown in using microbiota as a therapeutic?
inferred← citeshttps://doi.org/10.1111/mmi.14616openalex-snapshot
A clostripain‐like protease plays a major role in generating the secretome of enterotoxigenic Bacteroides fragilis
inferred← citeshttps://doi.org/10.1111/nyas.70255openalex-snapshot
Repurposing Drugs as Bacteroides fragilis BFT‐3 Inhibitors in the Animal Infection Model Galleria mellonella
inferred← citeshttps://doi.org/10.1111/prd.12371openalex-snapshot
Polymicrobial communities in periodontal disease: Their quasi‐organismal nature and dialogue with the host
inferred← citeshttps://doi.org/10.1126/scitranslmed.aah4669openalex-snapshot
Effects of a gut pathobiont in a gnotobiotic mouse model of childhood undernutrition
inferred← citeshttps://doi.org/10.1128/iai.00129-26openalex-snapshot
Outer membrane vesicles secreted by Bacteroides fragilis inhibit CFTR chloride secretion by human colon organoids
inferred← citeshttps://doi.org/10.1128/iai.00191-16openalex-snapshot
Bacteroides fragilis Enterotoxin Upregulates Heme Oxygenase-1 in Intestinal Epithelial Cells via a Mitogen-Activated Protein Kinase- and NF-κB-Dependent Pathway, Leading to Modulation of Apoptosis
inferred← citeshttps://doi.org/10.1128/iai.00312-19openalex-snapshot
Intestinal Epithelial Cells Exposed to Bacteroides fragilis Enterotoxin Regulate NF-κB Activation and Inflammatory Responses through β-Catenin Expression
inferred← citeshttps://doi.org/10.1128/jb.00342-15openalex-snapshot
Dps and DpsL Mediate SurvivalIn VitroandIn Vivoduring the Prolonged Oxidative Stress Response in Bacteroides fragilis
inferred← citeshttps://doi.org/10.1128/mbio.01232-16openalex-snapshot
Identification of a New Lipoprotein Export Signal in Gram-Negative Bacteria
inferred← citeshttps://doi.org/10.1128/mmbr.00225-25openalex-snapshot
Gene regulation in Bacteroides fragilis : adaptive control in a dynamic host environment
inferred← citeshttps://doi.org/10.1128/msystems.00653-23openalex-snapshot
Rocket-miR, a translational launchpad for miRNA-based antimicrobial drug development
inferred← citeshttps://doi.org/10.1128/spectrum.00013-22openalex-snapshot
Meta-Analysis of Altered Gut Microbiota Reveals Microbial and Metabolic Biomarkers for Colorectal Cancer
inferred← citeshttps://doi.org/10.1128/spectrum.01055-22openalex-snapshot
Colon Tumors in Enterotoxigenic Bacteroides fragilis (ETBF)-Colonized Mice Do Not Display a Unique Mutational Signature but Instead Possess Host-Dependent Alterations in the APC Gene
inferred← citeshttps://doi.org/10.1128/spectrum.03393-23openalex-snapshot
Bacteroides fragilis aggravates high-fat diet-induced non-alcoholic fatty liver disease by regulating lipid metabolism and remodeling gut microbiota
inferred← citeshttps://doi.org/10.1134/s0026893325700335openalex-snapshot
Gut Microbiota in Colorectal Cancer Carcinogenesis: The Evolution of Hypotheses
inferred← citeshttps://doi.org/10.1136/jitc-2024-008831openalex-snapshot
Inhibition of the NF-κB/HIF-1α signaling pathway in colorectal cancer by tyrosol: a gut microbiota-derived metabolite
inferred← citeshttps://doi.org/10.1146/annurev-cancerbio-030617-050240openalex-snapshot
The Impact of the Gut Microbiome on Colorectal Cancer
inferred← citeshttps://doi.org/10.1146/annurev-cancerbio-070120-095211openalex-snapshot
Gut Microbiota in Colorectal Cancer: Associations, Mechanisms, and Clinical Approaches
inferred← citeshttps://doi.org/10.1146/annurev-immunol-070119-115104openalex-snapshot
Interaction Between the Microbiota, Epithelia, and Immune Cells in the Intestine
inferred← citeshttps://doi.org/10.1146/annurev-med-080719-091604openalex-snapshot
Microbiota Effects on Carcinogenesis: Initiation, Promotion, and Progression
inferred← citeshttps://doi.org/10.1146/annurev-physiol-021014-071720openalex-snapshot
ADAM Proteases and Gastrointestinal Function
inferred← citeshttps://doi.org/10.1146/annurev-physiol-042022-025619openalex-snapshot
The Role of the Microbiome in the Etiopathogenesis of Colon Cancer
inferred← citeshttps://doi.org/10.1155/2016/2353560openalex-snapshot
The Dysregulation of Polyamine Metabolism in Colorectal Cancer Is Associated with Overexpression of c‐Myc and C/EBPβ rather than Enterotoxigenic Bacteroides fragilis Infection
inferred← citeshttps://doi.org/10.1155/2019/3405278openalex-snapshot
A Reasonable Diet Promotes Balance of Intestinal Microbiota: Prevention of Precolorectal Cancer
inferred← citeshttps://doi.org/10.1155/2019/5636272openalex-snapshot
The Four Horsemen in Colon Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-15-0749openalex-snapshot
Redundant Innate and Adaptive Sources of IL17 Production Drive Colon Tumorigenesis
inferred← citeshttps://doi.org/10.1158/0008-5472.can-17-0056openalex-snapshot
Mismatch Repair Proteins Initiate Epigenetic Alterations during Inflammation-Driven Tumorigenesis
inferred← citeshttps://doi.org/10.1158/1940-6207.capr-19-0286openalex-snapshot
Toll-like Receptor-6 Signaling Prevents Inflammation and Impacts Composition of the Microbiota During Inflammation-Induced Colorectal Cancer
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-15-0447openalex-snapshot
Regulatory T-cell Response to Enterotoxigenic Bacteroides fragilis Colonization Triggers IL17-Dependent Colon Carcinogenesis
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-15-0987openalex-snapshot
T Regulatory Cells Gone Bad: An Oncogenic Immune Response against Enterotoxigenic B. fragilis Infection Leads to Colon Cancer
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-20-0537openalex-snapshot
A Procarcinogenic Colon Microbe Promotes Breast Tumorigenesis and Metastatic Progression and Concomitantly Activates Notch and β-Catenin Axes
inferred← citeshttps://doi.org/10.1158/2326-6066.cir-17-0375openalex-snapshot
A Blueprint to Advance Colorectal Cancer Immunotherapies
inferred← citeshttps://doi.org/10.1159/000494052openalex-snapshot
Role of Gut Microbiota in the Development and Treatment of Colorectal Cancer
inferred← citeshttps://doi.org/10.1159/000508328openalex-snapshot
Gut Microbiota Dysbiosis Drives the Development of Colorectal Cancer
inferred← citeshttps://doi.org/10.11606/t.42.2020.tde-13012022-153608openalex-snapshot
Possível associação da presença de bactérias anaeróbias do trato gastrointestinal com a neoplasia retal: ocorrência e caracterização molecular bacteriana.
inferred← citeshttps://doi.org/10.11606/t.95.2019.tde-07022019-134344openalex-snapshot
Microbial community profiling of human gastrointestinal cancers
inferred← citeshttps://doi.org/10.1172/jci155101openalex-snapshot
Colorectal cancer: the facts in the case of the microbiota
inferred← citeshttps://doi.org/10.1172/jci160194openalex-snapshot
Gastrointestinal neoplasia: carcinogenic interaction between bile acids and Helicobacter pylori in the stomach
inferred← citeshttps://doi.org/10.1177/1534735419843178openalex-snapshot
Regulation of Shaoyao Ruangan Mixture on Intestinal Flora in Mice With Primary Liver Cancer
inferred← citeshttps://doi.org/10.1186/s12859-023-05197-0openalex-snapshot
Designing multi-epitope vaccine against important colorectal cancer (CRC) associated pathogens based on immunoinformatics approach
inferred← citeshttps://doi.org/10.1186/s12866-022-02465-6openalex-snapshot
The impact of the human microbiome in tumorigenesis, cancer progression, and biotherapeutic development
inferred← citeshttps://doi.org/10.1186/s12866-024-03354-wopenalex-snapshot
Detection of the antibiotic resistance genes content of intestinal Bacteroides, Parabacteroides and Phocaeicola isolates from healthy and carbapenem-treated patients from European countries
inferred← citeshttps://doi.org/10.1186/s12879-025-11624-9openalex-snapshot
Gut microbiota profiles associated with persistent anal HPV infection in men who have sex with men
inferred← citeshttps://doi.org/10.1186/s12885-020-6654-5openalex-snapshot
Temporal changes in gut microbiota profile in children with acute lymphoblastic leukemia prior to commencement-, during-, and post-cessation of chemotherapy
inferred← citeshttps://doi.org/10.1186/s12916-020-01584-zopenalex-snapshot
The impact of maternal and early life malnutrition on health: a diet-microbe perspective
inferred← citeshttps://doi.org/10.1186/s12929-018-0495-4openalex-snapshot
Pathobiont release from dysbiotic gut microbiota biofilms in intestinal inflammatory diseases: a role for iron?
inferred← citeshttps://doi.org/10.1186/s12943-021-01461-0openalex-snapshot
Crosstalk between autophagy and microbiota in cancer progression
inferred← citeshttps://doi.org/10.1186/s12943-025-02403-wopenalex-snapshot
The tumor microbiome in cancer progression: mechanisms and therapeutic potential
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