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dc.contributor.author Kirschner, Gyöngyi
dc.contributor.author Balla, Bernadett
dc.contributor.author Kósa, János
dc.contributor.author Horváth, Péter
dc.contributor.author Kovesdi A
dc.contributor.author Lakatos, Gergely
dc.contributor.author Takács, István
dc.contributor.author Nagy, Zsolt
dc.contributor.author Tóbiás, Bálint
dc.contributor.author Árvai, Kristóf
dc.contributor.author Lakatos, Péter
dc.date.accessioned 2018-09-24T07:47:06Z
dc.date.available 2018-09-24T07:47:06Z
dc.date.issued 2016
dc.identifier 84986253504
dc.identifier.citation pagination=1429-1437; journalVolume=157; journalIssueNumber=36; journalTitle=ORVOSI HETILAP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5872
dc.identifier.uri doi:10.1556/650.2016.30525
dc.description.abstract Tyrosine kinase inhibitors are widely used for treatment of certain oncohematological diseases. Several clinical studies have confirmed that specific BCR-ABL tyrosine kinase inhibitors alter the physiological process of bone tissue in a complex and unclearly identified manner. Since these treatments are being given to more and more patients, and the therapy takes decades or lasts even lifelong, it is justifiable to obtain more detailed knowledge of the molecular background of these mechanisms. In this article the authors summarize preliminary research results and human clinical observations on imatinib and nilotinib which are related to bone metabolism, and present the results of their own experiments in in vitro osteoblast cultures. Based on the presented results, the effects of imatinib and nilotinib on bone cells depend on the concentration of imatinib and nilotinib, the maturation stage of the cells and the distribution ratio of receptor tyrosine kinase signaling pathways. In this study the authors firstly prepared a stop-gap, comprehensive review in the Hungarian literature, regarding the effects of tyrosine kinase inhibitors on bone metabolism. In addition they firstly performed whole transcriptome analysis on osteoblasts in order to obtain a better understanding of the cellular molecular mechanisms. Orv. Hetil., 2016, 157(36), 1429-1437.
dc.relation.ispartof urn:issn:0030-6002
dc.title Az onkohematológiai betegségek kezelésében használt tirozinkináz-gátló imatinib és nilotinib csonthatásainak irodalmi áttekintése és a saját kutatási eredmények bemutatása
dc.type Journal Article
dc.date.updated 2018-07-17T10:17:59Z
dc.language.rfc3066 hu
dc.identifier.mtmt 3135008
dc.identifier.wos 000382796900002
dc.identifier.pubmed 27596510
dc.contributor.department SE/AOK/K/I. Sz. Belgyógyászati Klinika
dc.contributor.department SE/AOK/K/II. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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