Egyszerű nézet

dc.contributor.author Kovalszky, Ilona
dc.contributor.author Hjerpe A
dc.contributor.author Dobra K
dc.date.accessioned 2017-06-08T12:00:25Z
dc.date.available 2017-06-08T12:00:25Z
dc.date.issued 2014
dc.identifier.citation pagination=2491-2497; journalVolume=1840; journalIssueNumber=8; journalTitle=BIOCHIMICA ET BIOPHYSICA ACTA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2954
dc.identifier.uri doi:10.1016/j.bbagen.2014.04.015
dc.description.abstract BACKGROUND: Heparan sulfate proteoglycans (HSPGs) are important constituents of the cell membrane and they act as co-receptors for cellular signaling. Syndecan-1, glypican and perlecan also translocate to the nucleus in a regulated manner. Similar nuclear transport of growth factors and heparanase indicate a possible co-regulation and functional significance. SCOPE OF REVIEW: In this review we dissect the structural requirement for the nuclear translocation of HSPGs and their functional implications.s MAJOR CONCLUSIONS: The functions of the nuclear HSPGs are still incompletely understood. Evidence point to possible functions in hampering cell proliferation, inhibition of DNA topoisomerase I activity and inhibition of gene transcription. GENERAL SIGNIFICANCE: HSPGs influence the behavior of malignant tumors in many different ways. Modulating their functions may offer powerful tools to control fundamental biological processes and provide the basis for subsequent targeted therapies in cancer. This article is part of a Special Issue entitled Matrix-mediated cell behaviour and properties.
dc.relation.ispartof urn:issn:0006-3002
dc.title Nuclear translocation of heparan sulfate proteoglycans and their functional significance.
dc.type Journal Article
dc.date.updated 2015-12-07T13:29:31Z
dc.language.rfc3066 en
dc.identifier.mtmt 2708780
dc.identifier.wos 000339035400011
dc.identifier.pubmed 24780644
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.institution Semmelweis Egyetem


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