Egyszerű nézet

dc.contributor.author Széky, Balázs
dc.contributor.author Sillo P
dc.contributor.author Fábián, Melinda
dc.contributor.author Mayer, Balázs
dc.contributor.author Kárpáti, Sarolta
dc.contributor.author Németh, Krisztián
dc.date.accessioned 2018-09-24T06:44:16Z
dc.date.available 2018-09-24T06:44:16Z
dc.date.issued 2016
dc.identifier 84983316454
dc.identifier.citation pagination=1339-1348; journalVolume=157; journalIssueNumber=34; journalTitle=ORVOSI HETILAP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5886
dc.identifier.uri doi:10.1556/650.2016.30487
dc.description.abstract Over the past decade a rare cell population called cancer stem cells has been identified in both solid tumors and hematologic cancers. These cells are reminiscent of somatic and embryonic stem cells and play a critical role in the initiation and progression of malignancies. As all stem cells, they are able to undergo asymmetric cell division and hence renew themselves and create various other progenies with heterogenous phenotypes. A growing body of literature suggested that stem cell subpopulations contribute significantly to the growth and metastatic properties of melanoma. This review gives a comprehensive overview of the current literature on melanoma stem cells, with a special emphasis on the signaling pathways responsible for the homeostatic growth of melanocytes and the uncontrolled proliferation of melanoma cells. The importance of the local microenvironment are demonstrated through summarizing the role of various cell types, soluble factors and cell adhesion molecules in the progression of melanoma and the creation of treatment resistant cancer cell clones. Last but not least, the models of melanoma progression will be introduced and a variety of cellular markers will be presented that may be used to identify and therapeutically target melanoma. Orv. Hetil., 2016, 157(34), 1339-1348.
dc.relation.ispartof urn:issn:0030-6002
dc.title Tumorőssejtek szerepe a melanoma progressziójában és heterogenitásában
dc.type Journal Article
dc.date.updated 2018-07-17T11:15:50Z
dc.language.rfc3066 hu
dc.identifier.mtmt 3122282
dc.identifier.wos 000382796700001
dc.identifier.pubmed 27546799
dc.contributor.department SE/AOK/K/Bőr-, Nemikórtani és Bőronkológiai Klinika
dc.contributor.institution Semmelweis Egyetem


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