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Colorectal cancer-inflammatory bowel disease nexus and felony of Escherichia coli
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archinte.166.6.629openalex-snapshot
Associations Between the Age at Diagnosis and Location of Colorectal Cancer and the Use of Alcohol and Tobacco
inferredcites →https://doi.org/10.1002/ibd.22971openalex-snapshot
Multidrug Resistance Is Common in Escherichia coli Associated with Ileal Crohnʼs Disease
inferredcites →https://doi.org/10.1002/ijc.22314openalex-snapshot
Streptococcus bovis: Causal or incidental involvement in cancer of the colon?
inferredcites →https://doi.org/10.1002/ijc.25516openalex-snapshot
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
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Toxin-Induced Activation of Rho GTP-Binding Protein Increases Bcl-2 Expression and Influences Mitochondrial Homeostasis
inferredcites →https://doi.org/10.1007/978-3-319-35153-7_21openalex-snapshot
Epidemiology of Colorectal Cancer
inferredcites →https://doi.org/10.1007/s00384-004-0583-7openalex-snapshot
Activation of NF-?B in intestinal epithelial cells by E. coli strains isolated from the colonic mucosa of IBD patients
inferredcites →https://doi.org/10.1007/s10552-006-0072-0openalex-snapshot
Projecting the number of patients with colorectal carcinoma by phases of care in the US: 2000–2020
inferredcites →https://doi.org/10.1007/s10555-010-9217-4openalex-snapshot
Bacterial infections associated with cancer: possible implication in etiology with special reference to lateral gene transfer
inferredcites →https://doi.org/10.1007/s11882-015-0562-9openalex-snapshot
Immune Responses to Intestinal Microbes in Inflammatory Bowel Diseases
inferredcites →https://doi.org/10.1007/s12307-015-0177-7openalex-snapshot
IL-1 in Colon Inflammation, Colon Carcinogenesis and Invasiveness of Colon Cancer
inferredcites →https://doi.org/10.1016/j.amepre.2011.04.008openalex-snapshot
Productivity Savings from Colorectal Cancer Prevention and Control Strategies
inferredcites →https://doi.org/10.1016/j.canlet.2013.08.003openalex-snapshot
E. coli and colon cancer: Is mutY a culprit?
inferredcites →https://doi.org/10.1016/j.canlet.2015.04.024openalex-snapshot
Computational prediction of Escherichia coli proteins host subcellular targeting and their implications in colorectal cancer etiology
inferredcites →https://doi.org/10.1016/j.cell.2010.05.002openalex-snapshot
SnapShot: DNA Mismatch Repair
inferredcites →https://doi.org/10.1016/j.ddmec.2008.05.004openalex-snapshot
Inheritance of colorectal cancer
inferredcites →https://doi.org/10.1016/j.maturitas.2014.12.017openalex-snapshot
Diet and colorectal cancer
inferredcites →https://doi.org/10.1016/j.micpath.2013.02.002openalex-snapshot
Evaluation of the impact of quorum sensing transcriptional regulator SdiA on long-term persistence and fecal shedding of Escherichia coli O157:H7 in weaned calves
inferredcites →https://doi.org/10.1016/s0016-5085(03)00672-3openalex-snapshot
Bacteroides vulgatus protects against escherichia coli-induced colitis in gnotobiotic interleukin-2-deficient mice
inferredcites →https://doi.org/10.1016/s0016-5085(98)70019-8openalex-snapshot
Presence of adherent Escherichia coli strains in ileal mucosa of patients with Crohn's disease
inferredcites →https://doi.org/10.1021/acs.biomac.5b00413openalex-snapshot
Glycopolymers as Antiadhesives of E. coli Strains Inducing Inflammatory Bowel Diseases
inferredcites →https://doi.org/10.1038/ajgsup.2012.4openalex-snapshot
Intestinal Microbes in Inflammatory Bowel Diseases
inferredcites →https://doi.org/10.1038/ismej.2015.127openalex-snapshot
Microorganisms linked to inflammatory bowel disease-associated dysbiosis differentially impact host physiology in gnotobiotic mice
inferredcites →https://doi.org/10.1038/labinvest.2014.161openalex-snapshot
Intracellular colon cancer-associated Escherichia coli promote protumoral activities of human macrophages by inducing sustained COX-2 expression
inferredcites →https://doi.org/10.1038/ncomms8113openalex-snapshot
Interplay between enterobactin, myeloperoxidase and lipocalin 2 regulates E. coli survival in the inflamed gut
inferredcites →https://doi.org/10.1038/nri3896openalex-snapshot
Emerging cytokine networks in colorectal cancer
inferredcites →https://doi.org/10.1038/sj.onc.1209594openalex-snapshot
Succinate dehydrogenase and fumarate hydratase: linking mitochondrial dysfunction and cancer
inferredcites →https://doi.org/10.1053/gast.2002.30294openalex-snapshot
Mucosal flora in inflammatory bowel disease
inferredcites →https://doi.org/10.1053/j.gastro.2004.03.054openalex-snapshot
Enhanced Escherichia coli adherence and invasion in Crohn’s disease and colon cancer 1 1The authors thank Professor T. K. Korhonen (Division of General Microbiology, University of Helsinki, Finland), who kindly donated Escherichia coli IH11165; Professor J.-F. Colombel (Laboratoire de Recherche…
inferredcites →https://doi.org/10.1053/j.gastro.2004.04.061openalex-snapshot
High prevalence of adherent-invasive Escherichia coli associated with ileal mucosa in Crohn’s disease
inferredcites →https://doi.org/10.1053/j.gastro.2007.09.008openalex-snapshot
Toll-Like Receptor-4 Promotes the Development of Colitis-Associated Colorectal Tumors
inferredcites →https://doi.org/10.1053/j.gastro.2010.01.054openalex-snapshot
Hereditary and Familial Colon Cancer
inferredcites →https://doi.org/10.1053/j.gastro.2010.01.058openalex-snapshot
Inflammation and Colon Cancer
inferredcites →https://doi.org/10.1055/s-0029-1242458openalex-snapshot
Colorectal Cancer Epidemiology: Incidence, Mortality, Survival, and Risk Factors
inferredcites →https://doi.org/10.1080/10408360802485792openalex-snapshot
Intestinal bacteria and inflammatory bowel disease
inferredcites →https://doi.org/10.1089/cmb.2014.0001openalex-snapshot
In Silico Prediction of Escherichia coli Proteins Targeting the Host Cell Nucleus, with Special Reference to Their Role in Colon Cancer Etiology
inferredcites →https://doi.org/10.1093/bib/bbw093openalex-snapshot
Inter-kingdom prediction certainty evaluation of protein subcellular localization tools: microbial pathogenesis approach for deciphering host microbe interaction
inferredcites →https://doi.org/10.1093/jnci/djs354openalex-snapshot
Physical Activity and Risks of Proximal and Distal Colon Cancers: A Systematic Review and Meta-analysis
inferredcites →https://doi.org/10.1093/oxfordjournals.qjmed.a067890openalex-snapshot
Streptococcus bovis Bacteraemia Requires Rigorous Exclusion of Colonic Neoplasia and Endocarditis
inferredcites →https://doi.org/10.1097/01.mib.0000159663.62651.4fopenalex-snapshot
Molecular Characterization of Rectal Mucosa-Associated Bacterial Flora in Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1097/cji.0b013e3181d32e74openalex-snapshot
Cancer and Inflammation: Promise for Biologic Therapy
inferredcites →https://doi.org/10.1097/mib.0000000000000477openalex-snapshot
Immunoregulatory Pathways Involved in Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1101/cshperspect.a001651openalex-snapshot
The Nuclear Factor NF- B Pathway in Inflammation
inferredcites →https://doi.org/10.1101/gr.126516.111openalex-snapshot
Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00757.xopenalex-snapshot
Escherichia coli cyclomodulin Cif induces G2arrest of the host cell cycle without activation of the DNA-damage checkpoint-signalling pathway
inferredcites →https://doi.org/10.1111/j.1572-0241.2005.40237.xopenalex-snapshot
The Hamartomatous Polyposis Syndromes: A Clinical and Molecular Review
inferredcites →https://doi.org/10.1111/j.1572-0241.2005.41000.xopenalex-snapshot
Prevalence of Adenomas among Young Individuals at Average Risk for Colorectal Cancer
inferredcites →https://doi.org/10.1126/science.1224820openalex-snapshot
Intestinal Inflammation Targets Cancer-Inducing Activity of the Microbiota
inferredcites →https://doi.org/10.1128/iai.00067-06openalex-snapshot
Adherent and InvasiveEscherichia coliIs Associated with Granulomatous Colitis in Boxer Dogs
inferredcites →https://doi.org/10.1128/iai.00970-15openalex-snapshot
Campylobacter jejuni Increases Flagellar Expression and Adhesion of Noninvasive Escherichia coli: Effects on Enterocytic Toll-Like Receptor 4 and CXCL-8 Expression
inferredcites →https://doi.org/10.1128/iai.67.9.4499-4509.1999openalex-snapshot
Invasive Ability of an Escherichia coli Strain Isolated from the Ileal Mucosa of a Patient with Crohn’s Disease
inferredcites →https://doi.org/10.1128/mbio.00152-13openalex-snapshot
An Escherichia coli Effector Protein Promotes Host Mutation via Depletion of DNA Mismatch Repair Proteins
inferredcites →https://doi.org/10.1136/flgastro-2013-100329openalex-snapshot
The molecular genetics of colorectal cancer
inferredcites →https://doi.org/10.1136/gut.2006.099796openalex-snapshot
High prevalence of Escherichia coli belonging to the B2+D phylogenetic group in inflammatory bowel disease
inferredcites →https://doi.org/10.1136/gut.2006.111872openalex-snapshot
The role of Escherichia coli in inflammatory bowel disease
inferredcites →https://doi.org/10.1152/ajpcell.1997.273.4.c1160openalex-snapshot
Activation of NF-κB in intestinal epithelial cells by enteropathogenic Escherichia coli
inferredcites →https://doi.org/10.1158/2326-6066.cir-13-0101openalex-snapshot
Microbes and Inflammation in Colorectal Cancer
inferredcites →https://doi.org/10.1177/1756283x12473674openalex-snapshot
Microbial dysbiosis and colon carcinogenesis: could colon cancer be considered a bacteria-related disease?
inferredcites →https://doi.org/10.1186/gb-2012-13-9-r79openalex-snapshot
Dysfunction of the intestinal microbiome in inflammatory bowel disease and treatment
inferredcites →https://doi.org/10.1186/s13099-015-0050-8openalex-snapshot
Escherichia coli from Crohn’s disease patient displays virulence features of enteroinvasive (EIEC), enterohemorragic (EHEC), and enteroaggregative (EAEC) pathotypes
inferredcites →https://doi.org/10.1371/journal.pcbi.1003107openalex-snapshot
Bacteria-Human Somatic Cell Lateral Gene Transfer Is Enriched in Cancer Samples
inferredcites →https://doi.org/10.1371/journal.pone.0056964openalex-snapshot
High Prevalence of Mucosa-Associated E. coli Producing Cyclomodulin and Genotoxin in Colon Cancer
inferredcites →https://doi.org/10.18632/oncotarget.624openalex-snapshot
Infection, inflammation and colon carcinogenesis
inferredcites →https://doi.org/10.2174/156800911795538066openalex-snapshot
Cytokines, Inflammation and Colon Cancer
inferredcites →https://doi.org/10.2174/157339470903140220144227openalex-snapshot
Is it Possible to Reduce the Incident of Colorectal Cancer by Modifying Diet and Lifestyle?
inferredcites →https://doi.org/10.3389/fmicb.2015.00020openalex-snapshot
Microbiota disbiosis is associated with colorectal cancer
inferredcites →https://doi.org/10.3390/nu7031769openalex-snapshot
Macro- and Micronutrients Consumption and the Risk for Colorectal Cancer among Jordanians
inferredcites →https://doi.org/10.3390/toxins5081462openalex-snapshot
The Cytotoxic Necrotizing Factor 1 from E. Coli: A Janus Toxin Playing with Cancer Regulators
inferredcites →https://doi.org/10.3748/wjg.v20.i21.6560openalex-snapshot
Colon cancer-associated B2Escherichia colicolonize gut mucosa and promote cell proliferation
inferredcites →https://doi.org/10.4103/0971-5916.162091openalex-snapshot
Alterations of mucosal microbiota in the colon of patients with inflammatory bowel disease revealed by real time polymerase chain reaction amplification of 16S ribosomal ribonucleic acid
inferredcites →https://doi.org/10.4291/wjgp.v5.i3.213openalex-snapshot
Escherichia coli in chronic inflammatory bowel diseases: An update on adherent invasive Escherichia coli pathogenicity
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Lactobacillus johnsonii GLJ001 prevents DSS-induced colitis in mice by inhibiting M1 macrophage polarization via gut microbiota-SCFAs axis
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Physicochemical properties and antibacterial mechanism of theabrownins prepared from different catechins catalyzed by polyphenol oxidase and peroxidase
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Microbiome and colorectal cancer: Roles in carcinogenesis and clinical potential
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Colonic adenoma-associated Escherichia coli express specific phenotypes
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Atuação da equipe multiprofissional no cuidado ao paciente oncológico: um relato de experiência
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/24openalex-snapshot
Promoção da saúde no contexto da pandemia de COVID-19: relato de experiência
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/25openalex-snapshot
Análise de biomarcadores utilizados no diagnóstico, terapêutica e prognóstico do hepatoblastoma
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/26openalex-snapshot
Telessaúde e Atenção Primária à Saúde na pandemia: uma revisão narrativa
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/27openalex-snapshot
O enfrentamento emocional de profissionais da saúde cuidadores de pacientes oncológicos: revisão narrativa
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/28openalex-snapshot
Incidência dos casos de dengue na Região Oeste do Mato Grosso de 2015 a 2020
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/29openalex-snapshot
Mortalidade por Infarto Agudo do Miocárdio no Brasil de 2016 a 2020
inferred← citeshttps://doi.org/10.53524/lit.edt.978-65-84528-12-3/30openalex-snapshot
Taxa de internação por pneumonia na Região Centro-Oeste de 2017 a 2021
inferred← citeshttps://doi.org/10.70675/378e5eb7zd921z4f49z849cz258dce58c0a9openalex-snapshot
Loss of cyclin A2 contributes to colorectal carcinogenesis by disrupting colonic homeostasis and inducing inflammation in mice
inferred← citeshttps://doi.org/10.7150/ijbs.46405openalex-snapshot
The Gut-liver Axis in Immune Remodeling: New insight into Liver Diseases
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