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http://purl.uniprot.org/citations/21098094http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21098094http://www.w3.org/2000/01/rdf-schema#comment"Whereas the inhibition of vascular endothelial growth factor (VEGF) has shown promising results in sporadic colon cancer, the role of VEGF signaling in colitis-associated cancer (CAC) has not been addressed. We found that, unlike sporadic colorectal cancer and control patients, patients with CAC show activated VEGFR2 on intestinal epithelial cells (IECs). We then explored the function of VEGFR2 in a murine model of colitis-associated colon cancer characterized by increased VEGFR2 expression. Epithelial cells in tumor tissue expressed VEGFR2 and responded to VEGF stimulation with augmented VEGFR2-mediated proliferation. Blockade of VEGF function via soluble decoy receptors suppressed tumor development, inhibited tumor angiogenesis, and blocked tumor cell proliferation. Functional studies revealed that chronic inflammation leads to an up-regulation of VEGFR2 on IECs. Studies in conditional STAT3 mutant mice showed that VEGFR signaling requires STAT3 to promote epithelial cell proliferation and tumor growth in vivo. Thus, VEGFR-signaling acts as a direct growth factor for tumor cells in CAC, providing a molecular link between inflammation and the development of colon cancer."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.org/dc/terms/identifier"doi:10.1084/jem.20100438"xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Becker C."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Rose-John S."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Neurath M.F."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Wirtz S."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Weigmann B."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Neufert C."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Atreya R."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Vieth M."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Warntjen M."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Waldner M.J."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/author"Jefremow A."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/name"J Exp Med"xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/pages"2855-2868"xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/title"VEGF receptor signaling links inflammation and tumorigenesis in colitis-associated cancer."xsd:string
http://purl.uniprot.org/citations/21098094http://purl.uniprot.org/core/volume"207"xsd:string
http://purl.uniprot.org/citations/21098094http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21098094
http://purl.uniprot.org/citations/21098094http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/21098094
http://purl.uniprot.org/uniprot/#_A0A0G2JGF4-mappedCitation-21098094http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21098094
http://purl.uniprot.org/uniprot/#_A0A0U2WZU8-mappedCitation-21098094http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21098094
http://purl.uniprot.org/uniprot/#_A0A0U2X4C8-mappedCitation-21098094http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21098094
http://purl.uniprot.org/uniprot/#_A0A0H4A777-mappedCitation-21098094http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21098094