Egyszerű nézet

dc.contributor.author Oehme, F
dc.contributor.author Krahl, S
dc.contributor.author Győrffy, Balázs
dc.contributor.author Muessle, B
dc.contributor.author Rao, V
dc.contributor.author Greif, H
dc.contributor.author Ziegler, N
dc.contributor.author Lin, K
dc.contributor.author Thepkaysone, M-L
dc.contributor.author Polster, H
dc.contributor.author Tonn, T
dc.contributor.author Schneider, M
dc.contributor.author Weitz, J
dc.contributor.author Baenke, F
dc.contributor.author Kahlert, C
dc.date.accessioned 2021-09-15T11:35:41Z
dc.date.available 2021-09-15T11:35:41Z
dc.date.issued 2019
dc.identifier 85068585762
dc.identifier.citation journalVolume=16;journalIssueNumber=10;journalTitle=RNA BIOLOGY;pagerange=1339-1345;journalAbbreviatedTitle=RNA BIOL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8035
dc.identifier.uri doi:10.1080/15476286.2019.1637697
dc.description.abstract Molecular risk stratification of colorectal cancer can improve patient outcome. A panel of lncRNAs (H19, HOTTIP, HULC and MALAT1) derived from serum exosomes of patients with non-metastatic CRC and healthy donors was analyzed. Exosomes from healthy donors carried significantly more H19, HULC and HOTTIP transcripts in comparison to CRC patients. Correlation analysis between lncRNAs and clinical data revealed a statistical significance between low levels of exosomal HOTTIP and poor overall survival. This was confirmed by multivariate analysis that HOTTIP is an independent prognostic marker for overall survival (HR: 4.5, CI: 1.69–11.98, p = 0.0027). Here, HOTTIP poses to be a valid biomarker for patients with a CRC to predict post-surgical survival time. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
dc.format.extent 1339-1345
dc.relation.ispartof urn:issn:1547-6286
dc.title Low level of exosomal long non-coding RNA HOTTIP is a prognostic biomarker in colorectal cancer
dc.type Journal Article
dc.date.updated 2019-11-28T13:40:00Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 30816152
dc.identifier.wos 000474688500001
dc.identifier.pubmed 31251124
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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