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Expression of tight and adherens junction proteins in ulcerative colitis associated colorectal carcinoma: upregulation of claudin-1, claudin-3, claudin-4, and β-catenin

https://doi.org/10.1007/s00384-009-0653-y
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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/(sici)1097-010x(19971201)279:5<484::aid-jez11>3.0.co;2-8openalex-snapshot
Potential interplay between luminal growth factors and increased tight junction permeability in epithelial carcinogenesis
inferredcites →https://doi.org/10.1002/path.1201openalex-snapshot
Polarized distribution of carcinoembryonic antigen is associated with a tight junction molecule in human colorectal adenocarcinoma
inferredcites →https://doi.org/10.1007/s00384-006-0197-3openalex-snapshot
Differential expression of genes encoding tight junction proteins in colorectal cancer: frequent dysregulation of claudin-1, -8 and -12
inferredcites →https://doi.org/10.1007/s004390000375openalex-snapshot
Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancer
inferredcites →https://doi.org/10.1016/0016-5085(88)90541-0openalex-snapshot
Colorectal cancer in patients with ulcerative colitis
inferredcites →https://doi.org/10.1016/j.acthis.2007.02.007openalex-snapshot
Wnt pathway-related gene expression during malignant progression in ulcerative colitis
inferredcites →https://doi.org/10.1016/j.febslet.2005.09.091openalex-snapshot
Claudins upregulation in human colorectal cancer
inferredcites →https://doi.org/10.1016/j.humpath.2004.09.015openalex-snapshot
Claudins 2, 3, 4, and 5 in Paget’s disease and breast carcinoma
inferredcites →https://doi.org/10.1016/j.humpath.2005.05.019openalex-snapshot
Claudin expression in gastric adenocarcinomas: a tissue microarray study with prognostic correlation
inferredcites →https://doi.org/10.1016/s0002-9440(10)63051-9openalex-snapshot
Neutrophil Transmigration in Inflammatory Bowel Disease Is Associated with Differential Expression of Epithelial Intercellular Junction Proteins
inferredcites →https://doi.org/10.1016/s0016-5085(76)80465-9openalex-snapshot
On Calculating Cancer Risk and Survival of Ulcerative Colitis Patients with the Life Table Method
inferredcites →https://doi.org/10.1016/s0065-230x(08)60543-6openalex-snapshot
The Structure and Function of Intercellular Junctions in Cancer
inferredcites →https://doi.org/10.1016/s0079-6107(02)00037-8openalex-snapshot
Tight junction proteins
inferredcites →https://doi.org/10.1016/s0955-0674(00)00257-xopenalex-snapshot
Molecular architecture of adherens junctions
inferredcites →https://doi.org/10.1016/s0960-9822(00)00658-8openalex-snapshot
Tumor suppressors: Linking cell polarity and growth control
inferredcites →https://doi.org/10.1038/labinvest.2008.78openalex-snapshot
Claudin-1 and claudin-2 expression is elevated in inflammatory bowel disease and may contribute to early neoplastic transformation
inferredcites →https://doi.org/10.1038/modpathol.3800301openalex-snapshot
Claudin-1 is a strong prognostic indicator in stage II colonic cancer: a tissue microarray study
inferredcites →https://doi.org/10.1038/sj.onc.1206199openalex-snapshot
Loss of the tight junction protein claudin-7 correlates with histological grade in both ductal carcinoma in situ and invasive ductal carcinoma of the breast
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/emboj/19.9.2024openalex-snapshot
The tight junction protein ZO‐1 and an interacting transcription factor regulate ErbB‐2 expression
inferredcites →https://doi.org/10.1093/jnci/65.1.53openalex-snapshot
Tight Junctions in Epithelial Cells of Human Fetal Hindgut, Normal Colon, and Colon Adenocarcinoma 2
inferredcites →https://doi.org/10.1096/fj.04-3260comopenalex-snapshot
Interferon‐γ induces internalization of epithelial tight junction proteins via a macropinocytosis‐like process
inferredcites →https://doi.org/10.1097/00000658-197812000-00018openalex-snapshot
Cancer Risk in Extensive Ulcerative Colitis
inferredcites →https://doi.org/10.1111/j.1349-7006.2003.tb01485.xopenalex-snapshot
Cell adhesion system and human cancer morphogenesis
inferredcites →https://doi.org/10.1111/j.1600-0463.2008.00894.xopenalex-snapshot
Disturbed expression of E‐cadherin, beta‐catenin and tight junction proteins in colon carcinoma is unrelated to growth pattern and genetic polymorphisms
inferredcites →https://doi.org/10.1111/j.1749-6632.2000.tb05246.xopenalex-snapshot
Increased Tight Junction Permeability Can Result from Protein Kinase C Activation/Translocation and Act as a Tumor Promotional Event in Epithelial Cancers
inferredcites →https://doi.org/10.1126/stke.2162004pe2openalex-snapshot
Epithelial Barriers, Compartmentation, and Cancer
inferredcites →https://doi.org/10.1136/gut.31.7.800openalex-snapshot
Precancer and cancer in extensive ulcerative colitis: findings among 401 patients over 22 years.
inferredcites →https://doi.org/10.1146/annurev.ph.51.030189.004033openalex-snapshot
Development And Alteration Of Polarity
inferredcites →https://doi.org/10.1146/annurev.physiol.60.1.121openalex-snapshot
MOLECULAR ARCHITECTURE OF TIGHT JUNCTIONS
inferredcites →https://doi.org/10.1152/ajpcell.00038.2002openalex-snapshot
Claudins create charge-selective channels in the paracellular pathway between epithelial cells
inferredcites →https://doi.org/10.1152/ajpgi.1995.269.4.g467openalex-snapshot
Tight junctions and the molecular basis for regulation of paracellular permeability
inferredcites →https://doi.org/10.1158/0008-5472.can-07-5805openalex-snapshot
Defective Claudin-7 Regulation by Tcf-4 and Sox-9 Disrupts the Polarity and Increases the Tumorigenicity of Colorectal Cancer Cells
inferredcites →https://doi.org/10.1158/1541-7786.mcr-06-0384openalex-snapshot
A Complex of EpCAM, Claudin-7, CD44 Variant Isoforms, and Tetraspanins Promotes Colorectal Cancer Progression
inferredcites →https://doi.org/10.1159/000124978openalex-snapshot
Hypermethylation-Modulated Downregulation of Claudin-7 Expression Promotes the Progression of Colorectal Carcinoma
inferredcites →https://doi.org/10.1172/jci24543openalex-snapshot
Claudin-1 regulates cellular transformation and metastatic behavior in colon cancer
inferredcites →https://doi.org/10.14670/hh-16.1183openalex-snapshot
Tight junctions and their role in cancer metastasis.
inferredcites →https://doi.org/10.3727/096504001108747477openalex-snapshot
Involvement of Claudin-1 in the β-Catenin/Tcf Signaling Pathway and its Frequent Upregulation in Human Colorectal Cancers
inferredcites →https://doi.org/10.3892/or.19.4.953openalex-snapshot
Reduced expression of the claudin-7 gene correlates with venous invasion and liver metastasis in colorectal cancer
inferredcites →https://doi.org/10.4049/jimmunol.171.11.6164openalex-snapshot
Proinflammatory Cytokines Disrupt Epithelial Barrier Function by Apoptosis-Independent Mechanisms

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4513027openalex-extracted
inferred← citeshttps://doi.org/10.1002/ar.21163openalex-snapshot
Developmental Profile of Claudin‐3, ‐5, and ‐16 Proteins in the Epithelium of Chick Intestine
inferred← citeshttps://doi.org/10.1002/biof.138openalex-snapshot
Dysregulation of Claudin family genes in colorectal cancer in a Chinese population
inferred← citeshttps://doi.org/10.1002/btpr.2906openalex-snapshot
Evaluation of the preventive and therapeutic effects of a recombinant vector co‐expressing prostate‐specific stem cell antigen and Clostridium perfringens enterotoxin on prostate cancer in rats
inferred← citeshttps://doi.org/10.1002/cphy.c110045openalex-snapshot
Claudins and Other Tight Junction Proteins
inferred← citeshttps://doi.org/10.1002/ibd.21420openalex-snapshot
Role of different inflammatory and tumor biomarkers in the development of ulcerative colitis-associated carcinogenesis
inferred← citeshttps://doi.org/10.1002/iub.1347openalex-snapshot
Claudin clusters as determinants of epithelial barrier function
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2012.tb00450.xopenalex-snapshot
Claudins and Other Tight Junction Proteins
inferred← citeshttps://doi.org/10.1007/978-3-030-97204-2_6openalex-snapshot
Tight Junctions in the Inflamed Gut
inferred← citeshttps://doi.org/10.1007/978-3-319-94968-0_3openalex-snapshot
An Improved Particle Swarm Optimization with Dynamic Scale-Free Network for Detecting Multi-omics Features
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Tight Junctions in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-94-007-6028-8_9openalex-snapshot
Regulation of Tight Junctions for Therapeutic Advantages
inferred← citeshttps://doi.org/10.1007/s00424-014-1460-zopenalex-snapshot
Comparative analysis of theophylline and cholera toxin in rat colon reveals an induction of sealing tight junction proteins
inferred← citeshttps://doi.org/10.1007/s00424-016-1914-6openalex-snapshot
Active and passive involvement of claudins in the pathophysiology of intestinal inflammatory diseases
inferred← citeshttps://doi.org/10.1007/s00432-015-2011-5openalex-snapshot
CITED4 gene silencing in colorectal cancer cells modulates adherens/tight junction gene expression and reduces cell proliferation
inferred← citeshttps://doi.org/10.1007/s10330-020-0470-0openalex-snapshot
Future of targeted therapy for gastrointestinal cancer: Claudin 18.2
inferred← citeshttps://doi.org/10.1007/s10620-011-1688-9openalex-snapshot
Increase in the Tight Junction Protein Claudin-1 in Intestinal Inflammation
inferred← citeshttps://doi.org/10.1007/s10735-015-9610-yopenalex-snapshot
Claudin-3 and occludin tissue content in the glands of colonic mucosa with and without a fecal stream
inferred← citeshttps://doi.org/10.1007/s10787-024-01516-wopenalex-snapshot
Protective effects of ginsenosides on ulcerative colitis: a meta-analysis and systematic review to reveal the mechanisms of action
inferred← citeshttps://doi.org/10.1007/s12011-025-04819-3openalex-snapshot
Zinc Picolinate Mitigates Colonic Inflammation and Enhances Barrier Function in a Rat Model of Ulcerative Colitis
inferred← citeshttps://doi.org/10.1007/s12029-009-9070-2openalex-snapshot
β-Catenin Pathway in Ulcerative Colitis-Associated Colorectal Cancer and Therapeutic Implication
inferred← citeshttps://doi.org/10.1007/s12253-009-9217-2openalex-snapshot
Comparison of Beta-catenin with TGF-beta1, HIF-1alpha and Patients’ Disease-free Survival in Human Colorectal Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-382026-6.00038-5openalex-snapshot
Tight Junctions and the Intestinal Barrier
inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00025-6openalex-snapshot
Tight Junctions and the Intestinal Barrier
inferred← citeshttps://doi.org/10.1016/j.apjtm.2016.01.001openalex-snapshot
Effect of tight junction protein of intestinal epithelium and permeability of colonic mucosa in pathogenesis of injured colonic barrier during chronic recovery stage of rats with inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.bcp.2015.08.105openalex-snapshot
Resveratrol induces chemosensitization to 5-fluorouracil through up-regulation of intercellular junctions, Epithelial-to-mesenchymal transition and apoptosis in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.carbpol.2020.116958openalex-snapshot
Structural characteristics of a mannoglucan isolated from Chinese yam and its treatment effects against gut microbiota dysbiosis and DSS-induced colitis in mice
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.125599openalex-snapshot
Proteomic and transcriptomic changes in rat liver following oral feeding of formaldehyde
inferred← citeshttps://doi.org/10.1016/j.etap.2022.103833openalex-snapshot
Preventive empagliflozin activity on acute acetic acid-induced ulcerative colitis in rats via modulation of SIRT-1/PI3K/AKT pathway and improving colon barrier
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Single nucleotide variants c.-13G → C (rs17429833) and c.108C → T (rs72466472) in the CLDN1 gene and increased risk for familial colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.106645openalex-snapshot
Ginsenoside Rk3 alleviated DSS-induced ulcerative colitis by protecting colon barrier and inhibiting NLRP3 inflammasome pathway
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2015.12.001openalex-snapshot
Overexpressed Claudin-1 Can Be Visualized Endoscopically in Colonic Adenomas In Vivo
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Red lentil supplementation reduces the severity of dextran sodium sulfate-induced colitis in C57BL/6 male mice
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Attenuation of DSS induced colitis by Dictyophora indusiata polysaccharide (DIP) via modulation of gut microbiota and inflammatory related signaling pathways
inferred← citeshttps://doi.org/10.1016/j.neo.2023.100922openalex-snapshot
Medication adjustment of afatinib and combination therapy with sitagliptin for alleviating afatinib-induced diarrhea in rats
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Palmatine ameliorated murine colitis by suppressing tryptophan metabolism and regulating gut microbiota
inferred← citeshttps://doi.org/10.1016/j.stemcr.2020.03.021openalex-snapshot
The Snakeskin-Mesh Complex of Smooth Septate Junction Restricts Yorkie to Regulate Intestinal Homeostasis in Drosophila
inferred← citeshttps://doi.org/10.1016/s1063-5823(10)65013-2openalex-snapshot
Claudins in Cancer Biology
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c04433openalex-snapshot
Neohesperidin Attenuates DSS-Induced Ulcerative Colitis by Inhibiting Inflammation, Reducing Intestinal Barrier Damage, and Modulating Intestinal Flora Composition
inferred← citeshttps://doi.org/10.1021/acsptsci.4c00207openalex-snapshot
Cutaneous Application of Capsaicin Cream Reduces Clinical Signs of Experimental Colitis and Repairs Intestinal Barrier Integrity by Modulating the Gut Microbiota and Tight Junction Proteins
inferred← citeshttps://doi.org/10.1038/labinvest.2010.91openalex-snapshot
Enterohemorrhagic E. coli alters murine intestinal epithelial tight junction protein expression and barrier function in a Shiga toxin independent manner
inferred← citeshttps://doi.org/10.1038/mi.2015.142openalex-snapshot
AIM2 contributes to the maintenance of intestinal integrity via Akt and protects against Salmonella mucosal infection
inferred← citeshttps://doi.org/10.1038/mi.2016.128openalex-snapshot
Gut permeability and mucosal inflammation: bad, good or context dependent
inferred← citeshttps://doi.org/10.1039/d1fo02702fopenalex-snapshot
Anti-inflammatory and gut microbiota modulatory effects of polysaccharides from Fuzhuan brick tea on colitis in mice induced by dextran sulfate sodium
inferred← citeshttps://doi.org/10.1039/d3bm00591gopenalex-snapshot
Aloe-derived nanovesicles attenuate inflammation and enhance tight junction proteins for acute colitis treatment
inferred← citeshttps://doi.org/10.1042/bsr20181799openalex-snapshot
Maggot protein ameliorates dextran sulphate sodium-induced ulcerative colitis in mice
inferred← citeshttps://doi.org/10.1073/pnas.1017137108openalex-snapshot
Gain of chromosome band 7q11 in papillary thyroid carcinomas of young patients is associated with exposure to low-dose irradiation
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Anthocyanins/anthocyanidins and colorectal cancer: What is behind the scenes?
inferred← citeshttps://doi.org/10.1080/19336918.2018.1530933openalex-snapshot
Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
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Animal models for studying epithelial barriers in neonatal necrotizing enterocolitis, inflammatory bowel disease and colorectal cancer
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A transcriptomic score to classify the inflammation-dysplasia-cancer sequence lesions in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1097/mog.0b013e328354cc36openalex-snapshot
Cancer in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1099/acmi.0.000247openalex-snapshot
Microbiome in human cancers
inferred← citeshttps://doi.org/10.1100/tsw.2011.86openalex-snapshot
Epithelial Tight Junctional Changes in Colorectal Cancer Tissues
inferred← citeshttps://doi.org/10.1111/1440-1681.12321openalex-snapshot
Transplantation of human umbilical mesenchymal stem cells attenuates dextran sulfate sodium‐induced colitis in mice
inferred← citeshttps://doi.org/10.1111/j.1440-1827.2010.02587.xopenalex-snapshot
Immunohistochemical analysis of colorectal cancer with gastric phenotype: Claudin-18 is associated with poor prognosis
inferred← citeshttps://doi.org/10.1136/gutjnl-2018-316906openalex-snapshot
Tight junction proteins in gastrointestinal and liver disease
inferred← citeshttps://doi.org/10.1152/ajpgi.00002.2011openalex-snapshot
Lipid rafts are disrupted in mildly inflamed intestinal microenvironments without overt disruption of the epithelial barrier
inferred← citeshttps://doi.org/10.1152/ajpgi.00183.2012openalex-snapshot
Adalimumab prevents barrier dysfunction and antagonizes distinct effects of TNF-α on tight junction proteins and signaling pathways in intestinal epithelial cells
inferred← citeshttps://doi.org/10.1152/ajprenal.00058.2024openalex-snapshot
Intestinal barrier function declines during polycystic kidney disease progression
inferred← citeshttps://doi.org/10.1155/2021/2294942openalex-snapshot
The Role of lncRNAs in Regulating the Intestinal Mucosal Mechanical Barrier
inferred← citeshttps://doi.org/10.1159/000528084openalex-snapshot
Identification of Biomarkers Associated with the Prognoses of Colorectal Cancer Patients
inferred← citeshttps://doi.org/10.1186/s12885-017-3123-xopenalex-snapshot
Rapid eradication of colon carcinoma by Clostridium perfringens Enterotoxin suicidal gene therapy
inferred← citeshttps://doi.org/10.1258/ebm.2011.011269openalex-snapshot
Mucosal permeability is an intrinsic factor in susceptibility to dextran sulfate sodium-induced colitis in rats
inferred← citeshttps://doi.org/10.12998/wjcc.v10.i12.3647openalex-snapshot
Role of zonula occludens in gastrointestinal and liver cancers
inferred← citeshttps://doi.org/10.1369/0022155411418829openalex-snapshot
Expression of Claudins and Their Prognostic Significance in Noninvasive Urothelial Neoplasms of the Human Urinary Bladder
inferred← citeshttps://doi.org/10.1593/tlo.13412openalex-snapshot
Colon Macrophages Polarized by Commensal Bacteria Cause Colitis and Cancer through the Bystander Effect
inferred← citeshttps://doi.org/10.3109/08941939.2012.693334openalex-snapshot
E-Cadherin Expression in Colonic Mucosa with and Without Fecal Stream
inferred← citeshttps://doi.org/10.3382/ps.2012-02845openalex-snapshot
Effect of Saccharomyces boulardii and Bacillus subtilis B10 on intestinal ultrastructure modulation and mucosal immunity development mechanism in broiler chickens
inferred← citeshttps://doi.org/10.3389/fimmu.2019.01441openalex-snapshot
Claudin Family Participates in the Pathogenesis of Inflammatory Bowel Diseases and Colitis-Associated Colorectal Cancer
inferred← citeshttps://doi.org/10.3389/fmicb.2022.809086openalex-snapshot
Sodium Humate Alleviates Enterotoxigenic Escherichia coli-Induced Intestinal Dysfunction via Alteration of Intestinal Microbiota and Metabolites in Mice
inferred← citeshttps://doi.org/10.3390/cancers15164095openalex-snapshot
Expression of Claudins in Preneoplastic Conditions of the Gastrointestinal Tract: A Review
inferred← citeshttps://doi.org/10.3390/foods10061288openalex-snapshot
Natural Food Polysaccharides Ameliorate Inflammatory Bowel Disease and Its Mechanisms
inferred← citeshttps://doi.org/10.3390/foods14091514openalex-snapshot
Goat Milk-Derived Extracellular Vesicles Alleviate Colitis Potentially Through Improved Gut Microbiota in Mice
inferred← citeshttps://doi.org/10.3390/ijms140918407openalex-snapshot
Flavonoids from Orostachys japonicus A. Berger Inhibit the Invasion of LnCaP Prostate Carcinoma Cells by Inactivating Akt and Modulating Tight Junctions
inferred← citeshttps://doi.org/10.3390/ijms221910278openalex-snapshot
Effects of 1,2-Dimethylhydrazine on Barrier Properties of Rat Large Intestine and IPEC-J2 Cells
inferred← citeshttps://doi.org/10.3390/ijms25020703openalex-snapshot
Alkaline Phosphatase Relieves Colitis in Obese Mice Subjected to Forced Exercise via Its Anti-Inflammatory and Intestinal Microbiota-Shaping Properties
inferred← citeshttps://doi.org/10.3390/ijms26167968openalex-snapshot
Galactooligosaccharides Promote Gut Barrier Integrity and Exert Anti-Inflammatory Effects in DSS-Induced Colitis Through Microbiota Modulation
inferred← citeshttps://doi.org/10.3390/pharmaceutics16010029openalex-snapshot
Intestinal Membrane Function in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.3390/toxics10060296openalex-snapshot
The Effect of BPA-Treated Water on the Small Intestine via an In Vivo Study
inferred← citeshttps://doi.org/10.3390/toxins13030189openalex-snapshot
Assessing Mixture Effects of Cereulide and Deoxynivalenol on Intestinal Barrier Integrity and Uptake in Differentiated Human Caco-2 Cells
inferred← citeshttps://doi.org/10.3748/wjg.v22.i11.3117openalex-snapshot
Tight junctions in inflammatory bowel diseases and inflammatory bowel disease associated colorectal cancer
inferred← citeshttps://doi.org/10.3892/mmr.2013.1492openalex-snapshot
Inhibition of AGS human gastric cancer cell invasion and proliferation by Capsosiphon fulvescens glycoprotein
inferred← citeshttps://doi.org/10.3892/or.2012.1858openalex-snapshot
Anti-invasive effects of decitabine, a DNA methyltransferase inhibitor, through tightening of tight junctions and inhibition of matrix metalloproteinase activities in AGS human gastric carcinoma cells
inferred← citeshttps://doi.org/10.3969/j.issn.1673-4254.2017.01.11openalex-snapshot
[Claudin-3 expression in colorectal carcinoma and its significance].
inferred← citeshttps://doi.org/10.4103/egjp.egjp_29_21openalex-snapshot
Evaluation of the role of tight junction molecules
inferred← citeshttps://doi.org/10.4161/tisb.24978openalex-snapshot
Claudins in intestines
inferred← citeshttps://doi.org/10.4993/acrt.26.82openalex-snapshot
Relationship of the tight junction protein claudin-4 gene to outcomes in patients with colorectal cancer
inferred← citeshttps://doi.org/10.70675/7d878fb5z845dz4bd1z8dcaz40978f3a3e19openalex-snapshot
Étude des activités antioxydantes et anti-inflammatoires de métabolites secondaires bactériens produits directement dans l’eau, en modèles acellulaires, cellulaires et par la mise en place d’un modèle original de barrière intestinale
inferred← citeshttps://doi.org/10.70675/9002c99ez8e92z4779z9e11zb6d83f9bf057openalex-snapshot
Les claudines dans le cancer colorectal : ciblage thérapeutique de la claudine-1
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