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dc.contributor.author Bozóky Benedek
dc.contributor.author Savchenko Andrii
dc.contributor.author Csermely Péter
dc.contributor.author Korcsmáros Tamás
dc.contributor.author Dúl Zoltán
dc.contributor.author Pontén Fredrik
dc.contributor.author Székely László
dc.contributor.author Klein George
dc.date.accessioned 2017-01-20T11:23:20Z
dc.date.available 2017-01-20T11:23:20Z
dc.date.issued 2013
dc.identifier 84877815243
dc.identifier.citation pagination=286-293; journalVolume=133; journalIssueNumber=2; journalTitle=INTERNATIONAL JOURNAL OF CANCER;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2395
dc.identifier.uri doi:10.1002/ijc.28035
dc.description.abstract Increasing evidence indicates the importance of the tumor microenvironment, in particular cancer associated fibroblasts, in cancer development and progression. In this study we developed a novel, visually based method to identify new immunohistochemical signatures of these fibroblasts. The method employed a protein list based on 759 protein products of genes identified by RNA profiling from our previous study, comparing fibroblasts with differential growth modulating effect on human cancers cells, and their first neighbors in the human protein interactome. These 2,654 proteins were analyzed in the Human Protein Atlas online database by comparing their immunohistochemical expression patterns in normal vs. tumor associated fibroblasts. Twelve new proteins differentially expressed in cancer associated fibroblasts were identified (DLG1, BHLHE40, ROCK2, RAB31, AZI2, PKM2, ARHGAP31, ARHGAP26, ITCH, EGLN1, RNF19A, PLOD2), four of them can be connected to the Rho kinase signaling pathway. They were further analyzed in several additional tumor stromata and revealed that the majority showed congruence amongst the different tumors. Many of them were also positive in normal myofibroblast like cells. The new signatures can be useful in immunohistochemical analysis of different tumor stromata and may also give us an insight into the pathways activated in them in their true in vivo context. The method itself could be used for other similar analysis to identify proteins expressed in other cell types in tumors and their surrounding microenvironment. (c) 2013 Wiley Periodicals, Inc.
dc.relation.ispartof urn:issn:0020-7136
dc.title Novel signatures of cancer-associated fibroblasts.
dc.type Journal Article
dc.date.updated 2015-11-20T09:56:13Z
dc.language.rfc3066 en
dc.identifier.mtmt 2177176
dc.identifier.wos 000318951900004
dc.identifier.pubmed 23319410
dc.contributor.department SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.institution Semmelweis Egyetem


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