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dc.contributor.author Szász, Attila Marcell
dc.contributor.author Németh, Zsuzsanna
dc.contributor.author Győrffy, Balázs
dc.contributor.author Micsinai M
dc.contributor.author Krenács, Tibor
dc.contributor.author Baranyai, Zsolt
dc.contributor.author Harsányi, László
dc.contributor.author Kiss, András
dc.contributor.author Schaff, Zsuzsa
dc.contributor.author Tőkés, Anna-Mária
dc.contributor.author Kulka, Janina
dc.date.accessioned 2016-09-29T08:59:46Z
dc.date.available 2016-09-29T08:59:46Z
dc.date.issued 2011
dc.identifier 81855194325
dc.identifier.citation pagination=2248-2254; journalVolume=102; journalIssueNumber=12; journalTitle=CANCER SCIENCE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3071
dc.identifier.uri doi:10.1111/j.1349-7006.2011.02085.x
dc.description.abstract The elevated expression of claudins (CLDN) and E-cadherin (CDH-1) was found to correlate with poor prognostic features. Our aim was to perform a comprehensive analysis to assess their potential to predict prognosis in breast cancer. The expression of CLDN-1, -3-5, -7, -8, -10, -15, -18, and E-cadherin at the mRNA level was evaluated in correlation with survival in datasets containing expression measurements of 1809 breast cancer patients. The breast cancer tissues of 197 patients were evaluated with tissue microarray technique and immunohistochemical method for CLDN-1-5, -7, and E-cadherin protein expression. An additional validation set of 387 patients was used to test the accuracy of the resulting prognostic score. Based on the bioinformatic screening of publicly-available datasets, the metagene of CLDN-3, -4, -7, and E-cadherin was shown to have the most powerful predictive power in the survival analyses. An immunohistochemical protein profile consisting of CLDN-2, -4, and E-cadherin was able to predict outcome in the most effective manner in the training set. Combining the overlapping members of the above two methods resulted in the claudin-4 and E-cadherin score (CURIO), which was able to accurately predict relapse-free survival in the validation cohort (P=0.029). The multivariate analysis, including clinicopathological variables and the CURIO, showed that the latter kept its predictive power (P=0.040). Furthermore, the CURIO was able to further refine prognosis, separating good versus poor prognosis subgroups in luminal A, luminal B, and triple-negative breast cancer intrinsic subtypes. In breast cancer, the CURIO provides additional prognostic information besides the routinely utilized diagnostic approaches and factors. © 2011 Japanese Cancer Association.
dc.relation.ispartof urn:issn:1347-9032
dc.title Identification of a claudin-4 and E-cadherin score to predict prognosis in breast cancer
dc.type Journal Article
dc.date.updated 2016-02-03T08:18:23Z
dc.language.rfc3066 en
dc.identifier.mtmt 1816909
dc.identifier.wos 000297202800019
dc.identifier.pubmed 21883696
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.department SE/AOK/K/I. Sz. Sebészeti Klinika
dc.contributor.department SE/AOK/K/ISZGYK/MTA-SE Gyermekgyógyászati és Nephrológiai Kutatócsoport
dc.contributor.department SE/AOK/I/II. Sz. Patológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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