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Association of Fusobacterium nucleatum with clinical and molecular features in colorectal serrated pathway

https://doi.org/10.1002/ijc.29488
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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/ijc.10635openalex-snapshot
Are there two sides to colorectal cancer?
inferredcites →https://doi.org/10.1002/ijc.27674openalex-snapshot
Expression profiling shows differential molecular pathways and provides potential new diagnostic biomarkers for colorectal serrated adenocarcinoma
inferredcites →https://doi.org/10.1002/ijc.27869openalex-snapshot
Molecular patterns in the evolution of serrated lesion of the colorectum
inferredcites →https://doi.org/10.1002/ijc.28522openalex-snapshot
High miR-21 expression from FFPE tissues is associated with poor survival and response to adjuvant chemotherapy in colon cancer
inferredcites →https://doi.org/10.1002/ijc.28564openalex-snapshot
Possible role of Cdx2 in the serrated pathway of colorectal cancer characterized by BRAF mutation, high-level CpG Island methylator phenotype and mismatch repair-deficiency
inferredcites →https://doi.org/10.1002/ijc.28920openalex-snapshot
MicroRNA‐31 expression in relation to BRAF mutation, CpG island methylation and colorectal continuum in serrated lesions
inferredcites →https://doi.org/10.1007/s00535-012-0720-yopenalex-snapshot
Serrated polyps of the large intestine: current understanding of diagnosis, pathogenesis, and clinical management
inferredcites →https://doi.org/10.1007/s10096-014-2081-3openalex-snapshot
Fusobacterium nucleatum associates with stages of colorectal neoplasia development, colorectal cancer and disease outcome
inferredcites →https://doi.org/10.1007/s10552-011-9884-7openalex-snapshot
Aberrant crypt foci as predictors of colorectal neoplasia on repeat colonoscopy
inferredcites →https://doi.org/10.1016/j.anaerobe.2008.12.003openalex-snapshot
Phenotypic and genotypic analyses of clinical Fusobacterium nucleatum and Fusobacterium periodonticum isolates from the human gut
inferredcites →https://doi.org/10.1016/j.bbrc.2012.03.102openalex-snapshot
Porphyromonas gingivalis lipopolysaccharide induces miR-146a without altering the production of inflammatory cytokines
inferredcites →https://doi.org/10.1016/j.cell.2012.01.035openalex-snapshot
The Impact of the Gut Microbiota on Human Health: An Integrative View
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.2013.07.012openalex-snapshot
Fusobacterium nucleatum Promotes Colorectal Carcinogenesis by Modulating E-Cadherin/β-Catenin Signaling via its FadA Adhesin
inferredcites →https://doi.org/10.1016/j.chom.2014.02.007openalex-snapshot
Microbes, Microbiota, and Colon Cancer
inferredcites →https://doi.org/10.1016/j.femsim.2005.03.011openalex-snapshot
Periodontal pathogens: A quantitative comparison of anaerobic culture and real-time PCR
inferredcites →https://doi.org/10.1016/s0002-9270(02)03969-2openalex-snapshot
Changes in the bacterial flora of the neoterminal ileum after ileocolonic resection for Crohn's disease
inferredcites →https://doi.org/10.1034/j.1600-051x.2000.027010758.xopenalex-snapshot
Cytokine, elastase and oxygen radical release by Fusobacterium nucleatum‐activated leukocytes: a possible pathogenic factor in periodontitis
inferredcites →https://doi.org/10.1038/ajg.2012.161openalex-snapshot
Serrated Lesions of the Colorectum: Review and Recommendations From an Expert Panel
inferredcites →https://doi.org/10.1038/modpathol.2011.43openalex-snapshot
Up and downregulation of p16Ink4a expression in BRAF-mutated polyps/adenomas indicates a senescence barrier in the serrated route to colon cancer
inferredcites →https://doi.org/10.1038/nrc3610openalex-snapshot
The microbiome and cancer
inferredcites →https://doi.org/10.1038/nrc3611openalex-snapshot
Inflammation-induced cancer: crosstalk between tumours, immune cells and microorganisms
inferredcites →https://doi.org/10.1038/nrg3182openalex-snapshot
The human microbiome: at the interface of health and disease
inferredcites →https://doi.org/10.1053/j.gastro.2009.08.002openalex-snapshot
A Prospective Cohort Study Shows Unique Epigenetic, Genetic, and Prognostic Features of Synchronous Colorectal Cancers
inferredcites →https://doi.org/10.1053/j.gastro.2009.12.066openalex-snapshot
Role of the Serrated Pathway in Colorectal Cancer Pathogenesis
inferredcites →https://doi.org/10.1053/j.gastro.2013.10.060openalex-snapshot
Colorectal Carcinomas With CpG Island Methylator Phenotype 1 Frequently Contain Mutations in Chromatin Regulators
inferredcites →https://doi.org/10.1053/j.gastro.2014.01.001openalex-snapshot
Gastrointestinal Malignancy and the Microbiome
inferredcites →https://doi.org/10.1053/j.gastro.2014.03.001openalex-snapshot
The Intestinal Metabolome: An Intersection Between Microbiota and Host
inferredcites →https://doi.org/10.1093/carcin/bgp272openalex-snapshot
Inflammation and cancer: interweaving microRNA, free radical, cytokine and p53 pathways
inferredcites →https://doi.org/10.1093/carcin/bgt374openalex-snapshot
Association of microRNA-31 with BRAF mutation, colorectal cancer survival and serrated pathway
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a112652openalex-snapshot
DIET AND COLON CANCER
inferredcites →https://doi.org/10.1097/pas.0b013e3181e4f256openalex-snapshot
Longitudinal Outcome Study of Sessile Serrated Adenomas of the Colorectum: An Increased Risk for Subsequent Right-sided Colorectal Carcinoma
inferredcites →https://doi.org/10.1097/pas.0b013e318205df36openalex-snapshot
Sessile Serrated Adenoma With Early Neoplastic Progression
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/his.12055openalex-snapshot
The serrated pathway to colorectal carcinoma: current concepts and challenges
inferredcites →https://doi.org/10.1128/iai.01226-13openalex-snapshot
Diverse Toll-Like Receptors Mediate Cytokine Production by Fusobacterium nucleatum and Aggregatibacter actinomycetemcomitans in Macrophages
inferredcites →https://doi.org/10.1136/gut.2009.191320openalex-snapshot
Acute appendicitis is characterised by local invasion with Fusobacterium nucleatum / necrophorum
inferredcites →https://doi.org/10.1136/gut.2010.217182openalex-snapshot
Molecular pathological epidemiology of colorectal neoplasia: an emerging transdisciplinary and interdisciplinary field
inferredcites →https://doi.org/10.1136/gutjnl-2011-300865openalex-snapshot
Assessment of colorectal cancer molecular features along bowel subsites challenges the conception of distinct dichotomy of proximal versus distal colorectum
inferredcites →https://doi.org/10.1136/gutjnl-2012-302014openalex-snapshot
Colorectal cancer: a tale of two sides or a continuum?: Figure 1
inferredcites →https://doi.org/10.1136/gutjnl-2013-305209openalex-snapshot
Colorectal cancer: dichotomous or continuum model? Perhaps, a combination of both
inferredcites →https://doi.org/10.1158/0008-5472.can-13-1865openalex-snapshot
Fusobacterium in Colonic Flora and Molecular Features of Colorectal Carcinoma
inferredcites →https://doi.org/10.1186/1756-8722-5-66openalex-snapshot
MicroRNAs and Toll-like Receptor/Interleukin-1 Receptor Signaling
inferredcites →https://doi.org/10.1309/v8q9-kdd5-aj9l-nbagopenalex-snapshot
Small Colonic Microsatellite Unstable Adenocarcinomas and High-Grade Epithelial Dysplasias in Sessile Serrated Adenoma Polypectomy Specimens
inferredcites →https://doi.org/10.1371/journal.pone.0053653openalex-snapshot
Fusobacterium Is Associated with Colorectal Adenomas
inferredcites →https://doi.org/10.18632/oncotarget.3109openalex-snapshot
Association ofFusobacteriumspecies in pancreatic cancer tissues with molecular features and prognosis
inferredcites →https://doi.org/10.21775/cimb.013.025openalex-snapshot
Fusobacterium nucleatumin Periodontal Health and Disease
inferredcites →https://doi.org/10.2353/jmoldx.2006.050135openalex-snapshot
Precision and Performance Characteristics of Bisulfite Conversion and Real-Time PCR (MethyLight) for Quantitative DNA Methylation Analysis
inferredcites →https://doi.org/10.3748/wjg.v20.i29.10050openalex-snapshot
IGF2differentially methylated region hypomethylation in relation to pathological and molecular features of serrated lesions

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Association of Dietary Patterns With Risk of Colorectal Cancer Subtypes Classified by Fusobacterium nucleatum in Tumor Tissue
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Fusobacterium nucleatum Abundance is Associated with Cachexia in Colorectal Cancer Patients: The ColoCare Study
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Fusobacterium nucleatum impairs DNA mismatch repair and stability in patients with squamous cell carcinoma of the head and neck
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Fusobacterium nucleatum in cancer: Interactions with microbiota, tumour colonisation and cancer progression
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Invasive Fusobacterium nucleatum may play a role in the carcinogenesis of proximal colon cancer through the serrated neoplasia pathway
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Cancer‐associated fecal microbial markers in colorectal cancer detection
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Fusobacterium nucleatum and colorectal cancer: A mechanistic overview
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Intratumoral Fusobacterium nucleatum abundance correlates with macrophage infiltration and CDKN2A methylation in microsatellite-unstable colorectal carcinoma
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Fusobacterium Nucleatum Is a Risk Factor for Metastatic Colorectal Cancer
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Insights Into the Relationship Between Gut Microbiota and Colorectal Cancer
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Fusobacterium nucleatum and the Immune System in Colorectal Cancer
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Micro and nanoemulsions in colorectal cancer
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Metabolomics and proteomics in microbiome-cancer analysis
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Biosynthesis of meso-lanthionine in Fusobacterium nucleatum
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Fap2 Mediates Fusobacterium nucleatum Colorectal Adenocarcinoma Enrichment by Binding to Tumor-Expressed Gal-GalNAc
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FadA-positive Fusobacterium nucleatum is prevalent in biopsy specimens of Iranian patients with colorectal cancer
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A Fold Type II PLP-Dependent Enzyme from Fusobacterium nucleatum Functions as a Serine Synthase and Cysteine Synthase
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Fusobacterium nucleatum in Colorectal Carcinoma Tissue According to Tumor Location
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Potential influence of the microbiome environment in patients with biliary tract cancer and implications for therapy
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Structural basis of Fusobacterium nucleatum adhesin Fap2 interaction with receptors on cancer and immune cells
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Fusobacterium nucleatum is enriched in invasive biofilms in colorectal cancer
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Gut microbiota in colorectal cancer: mechanisms of action and clinical applications
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Fusobacterium nucleatum — symbiont, opportunist and oncobacterium
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Fusobacterium nucleatum: ecology, pathogenesis and clinical implications
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Metagenomic and metabolomic analyses reveal distinct stage-specific phenotypes of the gut microbiota in colorectal cancer
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Periodontitis is associated with an increased risk for proximal colorectal neoplasms
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Colorectal cancer-associated anaerobic bacteria proliferate in tumor spheroids and alter the microenvironment
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Association between Fusobacterium nucleatum and patient prognosis in metastatic colon cancer
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Fusobacterium nucleatum infection modulates the transcriptome and epigenome of HCT116 colorectal cancer cells in an oxygen-dependent manner
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Role of Fusobacteria in the serrated pathway of colorectal carcinogenesis
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Inhibition of the MurA enzyme in Fusobacterium nucleatum by potential inhibitors identified through computational and in vitro approaches
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WGCNA reveals key gene modules regulated by the combined treatment of colon cancer with PHY906 and CPT11
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Fusobacterium nucleatum Increases Proliferation of Colorectal Cancer Cells and Tumor Development in Mice by Activating Toll-Like Receptor 4 Signaling to Nuclear Factor−κB, and Up-regulating Expression of MicroRNA-21
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Tumor Potentiating Mechanisms of Fusobacterium nucleatum , A Multifaceted Microbe
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Association Between Risk Factors for Colorectal Cancer and Risk of Serrated Polyps and Conventional Adenomas
inferred← citeshttps://doi.org/10.1053/j.gastro.2019.06.048openalex-snapshot
Influence of the Gut Microbiome, Diet, and Environment on Risk of Colorectal Cancer
inferred← citeshttps://doi.org/10.1053/j.seminoncol.2019.08.003openalex-snapshot
An updated review of microsatellite instability in the era of next-generation sequencing and precision medicine
inferred← citeshttps://doi.org/10.1055/s-0042-110193openalex-snapshot
Mikrobielle Biomarker zur Krebsfrüherkennung
inferred← citeshttps://doi.org/10.1055/s-0043-124940openalex-snapshot
Mikrobielle Biomarker zur Krebsfrüherkennung
inferred← citeshttps://doi.org/10.1080/14737159.2017.1337511openalex-snapshot
Genetic and epigenetic markers in colorectal cancer screening: recent advances
inferred← citeshttps://doi.org/10.1080/19490976.2018.1445957openalex-snapshot
Systematic review: Gut microbiota in fecal samples and detection of colorectal neoplasms
inferred← citeshttps://doi.org/10.1080/19490976.2020.1854641openalex-snapshot
Microbiome distinctions between the CRC carcinogenic pathways
inferred← citeshttps://doi.org/10.1080/19490976.2020.1863135openalex-snapshot
Serrated neoplasia in the colorectum: gut microbiota and molecular pathways
inferred← citeshttps://doi.org/10.1080/19490976.2023.2185028openalex-snapshot
Intestinal bacteria and colorectal cancer: etiology and treatment
inferred← citeshttps://doi.org/10.1080/19490976.2023.2263934openalex-snapshot
Colorectal cancer–associated T cell receptor repertoire abnormalities are linked to gut microbiome shifts and somatic cell mutations
inferred← citeshttps://doi.org/10.1080/19490976.2023.2295384openalex-snapshot
Fusobacterium nucleatum promotes inflammatory and anti-apoptotic responses in colorectal cancer cells via ADP-heptose release and ALPK1/TIFA axis activation
inferred← citeshttps://doi.org/10.1080/19490976.2024.2310215openalex-snapshot
Colibactin-producing Escherichia coli enhance resistance to chemotherapeutic drugs by promoting epithelial to mesenchymal transition and cancer stem cell emergence
inferred← citeshttps://doi.org/10.1080/20002297.2022.2145729openalex-snapshot
Fusobacterium nucleatum and its associated systemic diseases: epidemiologic studies and possible mechanisms
inferred← citeshttps://doi.org/10.1093/carcin/bgx013openalex-snapshot
MicroRNA-196b is an independent prognostic biomarker in patients with pancreatic cancer
inferred← citeshttps://doi.org/10.1093/carcin/bgx053openalex-snapshot
Fusobacterium and colorectal cancer: causal factor or passenger? Results from a large colorectal cancer screening study
inferred← citeshttps://doi.org/10.1093/carcin/bgx092openalex-snapshot
Fusobacterium and colorectal carcinogenesis
inferred← citeshttps://doi.org/10.1093/jb/mvx080openalex-snapshot
Crosstalk between the microbiome and epigenome: messages from bugs
inferred← citeshttps://doi.org/10.1093/jncics/pkab037openalex-snapshot
Two-Sample Mendelian Randomization Analysis of Associations Between Periodontal Disease and Risk of Cancer
inferred← citeshttps://doi.org/10.1097/cco.0000000000000927openalex-snapshot
The role of Fusobacteria in oral cancer and immune evasion
inferred← citeshttps://doi.org/10.1097/md.0000000000017221openalex-snapshot
Prognostic impact of the Fusobacterium nucleatum status in colorectal cancers
inferred← citeshttps://doi.org/10.1097/md.0000000000035336openalex-snapshot
Factors influencing age at onset of colorectal polyps and benefit-finding after polypectomy
inferred← citeshttps://doi.org/10.1097/ppo.0000000000000744openalex-snapshot
Advancements in Understanding and Preventing Obesity-Related Colon Cancer
inferred← citeshttps://doi.org/10.1099/mgen.0.000300openalex-snapshot
A survey of Fusobacterium nucleatum genes modulated by host cell infection
inferred← citeshttps://doi.org/10.1101/2020.12.21.423755openalex-snapshot
Fusobacterium nucleatum facilitates cetuximab resistance in colorectal cancer via the PI3K/AKT and JAK/STAT3 pathways
inferred← citeshttps://doi.org/10.1101/2024.02.28.582045openalex-snapshot
Structural basis of Fusobacterium nucleatum adhesin Fap2 interaction with receptors on cancer and immune cells
inferred← citeshttps://doi.org/10.1109/tmag.2022.3161508openalex-snapshot
A Detection and Analysis of Fusobacterium Utilizing Changes in the Magnetic Properties of Magnetic Nanoparticles-Antibody–Antigen Aggregates
inferred← citeshttps://doi.org/10.1111/jgh.15559openalex-snapshot
Fecal Fusobacterium nucleatum as a predictor for metachronous colorectal adenoma after endoscopic polypectomy
inferred← citeshttps://doi.org/10.1111/jre.70165openalex-snapshot
The Dual Face of Fusobacterium nucleatum in Cancer: Foe, Friend or Both?
inferred← citeshttps://doi.org/10.11134/btp.1.2024.3openalex-snapshot
MOLECULAR DETECTION OF FUSOBACTERIUM NUCLEATUM IN IN KAZAKHSTANY PATIENTS WITH COLORECTAL CANCER
inferred← citeshttps://doi.org/10.1126/science.aal5240openalex-snapshot
Analysis of Fusobacterium persistence and antibiotic response in colorectal cancer
inferred← citeshttps://doi.org/10.1128/mbio.02706-20openalex-snapshot
Fusobacterium nucleatum Secretes Outer Membrane Vesicles and Promotes Intestinal Inflammation
inferred← citeshttps://doi.org/10.1128/msystems.00622-26openalex-snapshot
Integrative microbiome–methylome analysis links bacterial taxa to colorectal cancer histological subtypes
inferred← citeshttps://doi.org/10.1128/spectrum.05123-22openalex-snapshot
Strain-level detection of Fusobacterium nucleatum in colorectal cancer specimens by targeting the CRISPR–Cas region
inferred← citeshttps://doi.org/10.1136/gutjnl-2015-310101openalex-snapshot
Fusobacterium nucleatum in colorectal carcinoma tissue and patient prognosis
inferred← citeshttps://doi.org/10.1136/gutjnl-2017-315537openalex-snapshot
Integrative analysis of exogenous, endogenous, tumour and immune factors for precision medicine
inferred← citeshttps://doi.org/10.1136/gutjnl-2021-325193openalex-snapshot
Patients with mesenchymal tumours and high Fusobacteriales prevalence have worse prognosis in colorectal cancer (CRC)
inferred← citeshttps://doi.org/10.11405/nisshoshi.113.1878openalex-snapshot
Association of colorectal carcinogenesis pathway with life style and intestinal microbiome based on the genome and epigenome abnormalities.
inferred← citeshttps://doi.org/10.1146/annurev-micro-102215-095513openalex-snapshot
Gut Microbiota, Inflammation, and Colorectal Cancer
inferred← citeshttps://doi.org/10.1146/annurev-pathmechdis-012418-012818openalex-snapshot
Insights into Pathogenic Interactions Among Environment, Host, and Tumor at the Crossroads of Molecular Pathology and Epidemiology
inferred← citeshttps://doi.org/10.1155/2019/5636272openalex-snapshot
The Four Horsemen in Colon Cancer
inferred← citeshttps://doi.org/10.1155/2023/7429949openalex-snapshot
An Insight on Gut Flora, Colorectal Cancer Mechanism, and Treatment Strategies
inferred← citeshttps://doi.org/10.1155/cjgh/2782582openalex-snapshot
Navigating the Terrain of Post‐Polypectomy Surveillance: Charting the Complex Landscape of Guidelines and Recurrence Risks
inferred← citeshttps://doi.org/10.1158/1055-9965.epi-18-1295openalex-snapshot
Fusobacterium nucleatum in the Colorectum and Its Association with Cancer Risk and Survival: A Systematic Review and Meta-analysis
inferred← citeshttps://doi.org/10.1158/1055-9965.epi-24-1020openalex-snapshot
Highly Sensitive DNA Testing of Fusobacterium nucleatum in Colorectal Tumors
inferred← citeshttps://doi.org/10.1158/1055-9965.epi-25-1580openalex-snapshot
The Phylum Fusobacteriota Is Associated with Colorectal Cancer–Specific Mortality: Results from the Translational Research Program in Cancer Differences across Populations
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-16-1786openalex-snapshot
Human Microbiome Fusobacterium Nucleatum in Esophageal Cancer Tissue Is Associated with Prognosis
inferred← citeshttps://doi.org/10.1158/1940-6207.capr-16-0178openalex-snapshot
Fusobacterium Nucleatum Subspecies Animalis Influences Proinflammatory Cytokine Expression and Monocyte Activation in Human Colorectal Tumors
inferred← citeshttps://doi.org/10.1158/1940-6207.capr-16-0264openalex-snapshot
Sessile Serrated Polyps and Colon Cancer Prevention
inferred← citeshttps://doi.org/10.1158/2767-9764.crc-22-0248openalex-snapshot
Circulating IgA Antibodies Against Fusobacterium nucleatum Amyloid Adhesin FadA are a Potential Biomarker for Colorectal Neoplasia
inferred← citeshttps://doi.org/10.1158/2767-9764.crc-23-0179openalex-snapshot
Fusobacterium nucleatum Load Correlates with KRAS Mutation and Sessile Serrated Pathogenesis in Colorectal Adenocarcinoma
inferred← citeshttps://doi.org/10.1159/000496102openalex-snapshot
Mucosa-Associated Microbiota in the Gastrointestinal Tract of Healthy Japanese Subjects
inferred← citeshttps://doi.org/10.1159/000512175openalex-snapshot
The Role of Fusobacterium nucleatum in Colorectal Carcinogenesis
inferred← citeshttps://doi.org/10.1177/1724600818781301openalex-snapshot
Fecal fusobacterium nucleatum for detecting colorectal cancer: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1177/2050640619890732openalex-snapshot
First steps towards combining faecal immunochemical testing with the gut microbiome in colorectal cancer screening
inferred← citeshttps://doi.org/10.1186/s12866-021-02352-6openalex-snapshot
Fusobacterium nucleatum predicts a high risk of metastasis for esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1186/s12885-021-08903-4openalex-snapshot
Fusobacterium nucleatum and oral cancer: a critical review
inferred← citeshttps://doi.org/10.1186/s12935-021-01886-zopenalex-snapshot
The dysbiosis signature of Fusobacterium nucleatum in colorectal cancer-cause or consequences? A systematic review
inferred← citeshttps://doi.org/10.1186/s12967-024-05720-8openalex-snapshot
Parvimonas micra forms a distinct bacterial network with oral pathobionts in colorectal cancer patients
inferred← citeshttps://doi.org/10.1186/s13027-021-00381-4openalex-snapshot
Association between colorectal cancer and Fusobacterium nucleatum and Bacteroides fragilis bacteria in Iranian patients: a preliminary study
inferred← citeshttps://doi.org/10.1186/s13027-021-00410-2openalex-snapshot
Evaluating the presence of Mycoplasma hyorhinis, Fusobacterium nucleatum, and Helicobacter pylori in biopsies of patients with gastric cancer
inferred← citeshttps://doi.org/10.1186/s13046-020-01801-wopenalex-snapshot
BRAFV600E mutation impinges on gut microbial markers defining novel biomarkers for serrated colorectal cancer effective therapies
inferred← citeshttps://doi.org/10.1186/s13643-019-1031-7openalex-snapshot
Is a fusobacterium nucleatum infection in the colon a risk factor for colorectal cancer?: a systematic review and meta-analysis protocol
inferred← citeshttps://doi.org/10.1186/s13643-020-01526-zopenalex-snapshot
Detection of Fusobacterium nucleatum in feces and colorectal mucosa as a risk factor for colorectal cancer: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1186/s40168-016-0218-6openalex-snapshot
The gut microbiota in conventional and serrated precursors of colorectal cancer
inferred← citeshttps://doi.org/10.1245/s10434-018-6681-5openalex-snapshot
Association Between Fusobacterium nucleatum, Pathway Mutation, and Patient Prognosis in Colorectal Cancer
inferred← citeshttps://doi.org/10.12865/chsj.44.02.08openalex-snapshot
Colorectal Cancer Biomarkers - A New Trend in Early Diagnosis.
inferred← citeshttps://doi.org/10.1371/journal.pone.0262416openalex-snapshot
Fusobacterium nucleatum and Bacteroides fragilis detection in colorectal tumours: Optimal target site and correlation with total bacterial load
inferred← citeshttps://doi.org/10.1371/journal.pone.0269541openalex-snapshot
Detection of Fusobacterium nucleatum DNA in primary care patient stool samples does not predict progression of colorectal neoplasia
inferred← citeshttps://doi.org/10.1515/cclm-2017-1163openalex-snapshot
Exploring the microbiota to better understand gastrointestinal cancers physiology
inferred← citeshttps://doi.org/10.1515/med-2020-0226openalex-snapshot
Serrated lesions of the colon and rectum: Emergent epidemiological data and molecular pathways
inferred← citeshttps://doi.org/10.15403/jgld-507openalex-snapshot
Correlation of Metabolic Risk Factors with Sessile Serrated Lesions
inferred← citeshttps://doi.org/10.15430/jcp.2017.22.2.108openalex-snapshot
Comparisons of Gut Microbiota Among Healthy Control, Patients With Conventional Adenoma, Sessile Serrated Adenoma, and Colorectal Cancer
inferred← citeshttps://doi.org/10.1586/14737159.2016.1115346openalex-snapshot
Integration of molecular pathology, epidemiology and social science for global precision medicine
inferred← citeshttps://doi.org/10.17709/2410-1893-2024-11-3-7openalex-snapshot
Features of the microbiota for various malignant neoplasms
inferred← citeshttps://doi.org/10.18027/2224-5057-2019-9-2-5-11openalex-snapshot
The Role of the Intestinal Microbiome in the Immunotherapy of Colon Cancer
inferred← citeshttps://doi.org/10.18027/2224-5057-2020-10-3s1-60-62openalex-snapshot
Роль кишечной микробиоты в патогенезе колоректального рака. Обзор литературных данных
inferred← citeshttps://doi.org/10.18632/oncotarget.13628openalex-snapshot
What influences preneoplastic colorectal lesion recurrence?
inferred← citeshttps://doi.org/10.18632/oncotarget.18716openalex-snapshot
Potential link between Fusobacterium enrichment and DNA methylation accumulation in the inflammatory colonic mucosa in ulcerative colitis
inferred← citeshttps://doi.org/10.20517/cdr.2021.144openalex-snapshot
Fusobacterium nucleatum: a new player in regulation of cancer development and therapeutic response
inferred← citeshttps://doi.org/10.21037/jgo.2020.02.03openalex-snapshot
The role of oral health in gastrointestinal malignancies
inferred← citeshttps://doi.org/10.21037/tgh.2017.01.05openalex-snapshot
Post-colonoscopy colorectal cancer: the key role of molecular pathological epidemiology
inferred← citeshttps://doi.org/10.21037/tlcr.2019.10.03openalex-snapshot
Optimizing selection of candidates for lung cancer screening: role of comorbidity, frailty and life expectancy
inferred← citeshttps://doi.org/10.21203/rs.3.rs-101163/v1openalex-snapshot
Fusobacterium Nucleatum Predicts a Risk for Esophageal Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1077771/v1openalex-snapshot
Diet, microbes, and cancer across the tree of life: a systematic review
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2553053/v1openalex-snapshot
Lifestyle factors and the risk associated with conventional adenomas and serrated polyps among healthy people undergoing a medical checkup
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7874624/v1openalex-snapshot
PIK3CA-Mutated Colorectal Cancer Exhibits a Unique Gut Dysbiosis Profile: Insights from a Nationwide Pan-Cancer Screen in Japan
inferred← citeshttps://doi.org/10.2139/ssrn.3520024openalex-snapshot
Integrative Analysis of Fecal Metagenomics and Metabolomics in Colorectal Cancer
inferred← citeshttps://doi.org/10.2147/cmar.s382464openalex-snapshot
Clinical Significance of Fusobacterium nucleatum and Microsatellite Instability in Evaluating Colorectal Cancer Prognosis
inferred← citeshttps://doi.org/10.2147/idr.s357922openalex-snapshot
Fusobacterium nucleatum and Colorectal Cancer
inferred← citeshttps://doi.org/10.2147/ott.s145949openalex-snapshot
Clinical significance of Fusobacterium nucleatum, epithelial–mesenchymal transition, and cancer stem cell markers in stage III/IV colorectal cancer patients
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.s194153openalex-snapshot
Oral microbiota and gastrointestinal cancer
inferred← citeshttps://doi.org/10.2174/0113892010338997241216053634openalex-snapshot
Potential Pathogens Associated with Colorectal Cancer
inferred← citeshttps://doi.org/10.2174/0115733947270529231116114913openalex-snapshot
Alterations of the Gut Microbiome and Metabolome Following: A Opportunity for Early Detection of Colorectal Cancer
inferred← citeshttps://doi.org/10.2174/1871526520666200720113004openalex-snapshot
Proliferative Effect of FadA Recombinant Protein from Fusobacterium nucleatum on SW480 Colorectal Cancer Cell Line
inferred← citeshttps://doi.org/10.2196/89422openalex-snapshot
Development of an Interpretable Triage Tool for Colorectal Polyp Risk Stratification Within a Population-Based Screening Program: Machine Learning Approach
inferred← citeshttps://doi.org/10.2217/bmm-2019-0020openalex-snapshot
Analysis of FUSOBACTERIUM NUCLEATUM and Streptococcus Gallolyticus in Saliva of Colorectal Cancer Patients
inferred← citeshttps://doi.org/10.2217/pgs-2020-0044openalex-snapshot
Predictive Values of Colon Microbiota in the Treatment Response to Colorectal Cancer
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