Egyszerű nézet

dc.contributor.author Speer, Gábor
dc.contributor.author Cseh, Károly
dc.contributor.author Winkler, Gábor
dc.contributor.author Takács, István
dc.contributor.author Barna, István
dc.contributor.author Nagy, Zsolt
dc.contributor.author Lakatos, Péter
dc.date.accessioned 2016-07-21T13:16:39Z
dc.date.available 2016-07-21T13:16:39Z
dc.date.issued 2001
dc.identifier 0034884947
dc.identifier.citation pagination=1463-1468; journalVolume=37; journalIssueNumber=12; journalTitle=EUROPEAN JOURNAL OF CANCER;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3389
dc.identifier.uri doi:10.1016/S0959-8049(01)00139-3
dc.description.abstract Oestrogen/oestrogen receptor (ER) and vitamin D/vitamin D receptor (VDR) systems have been implicated in the pathogenesis of colorectal cancers. The expression of erbB-2 and epidermal growth factor receptor (EGFR) in colorectal cancers has been suggested to have diagnostic and prognostic significance. In our study, XbaI and PvuII polymorphisms of the ER gene and the BsmI polymorphism of the VDR gene were studied in 56 Caucasian patients with rectal cancer. The relationship between the ER and VDR genotypes and the expression of oncogenes was also investigated. The presence of the x allele of ER gene significantly correlated with the overexpression of the erbB-2 and EGFR oncogenes. Significantly increased erbB-2 expression was observed in patients with the VDR B allele. The XXbb allelic combination of the ER/VDR genes was associated with a significantly lower erbB-2 expression, whereas in the other genotypes significantly higher oncogene expression was seen. Our data raise the possibility that ER/VDR gene polymorphisms accompanied by variable oncogene expression might influence the pathogenetic processes of colorectal cancers.
dc.relation.ispartof urn:issn:0959-8049
dc.title Oestrogen and vitamin D receptor (VDR) genotypes and the expression of ErbB-2 and EGF receptor in human rectal cancers.
dc.type Journal Article
dc.date.updated 2016-04-28T07:10:21Z
dc.language.rfc3066 en
dc.identifier.mtmt 1335568
dc.identifier.wos 000170407200008
dc.identifier.pubmed 11506951
dc.contributor.department SE/AOK/K/I. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote EIN: Eur J Cancer 2001 Oct;37(15):1963


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