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dc.contributor.author Bugyik, Edina
dc.contributor.author Dezső, Katalin
dc.contributor.author Reiniger, Lilla
dc.contributor.author Laszlo, Viktoria
dc.contributor.author Tóvári, József
dc.contributor.author Tímár, József
dc.contributor.author Nagy, Péter
dc.contributor.author Klepetko W
dc.contributor.author Döme, Balázs
dc.contributor.author Paku, Sándor
dc.date.accessioned 2016-08-25T15:35:01Z
dc.date.available 2016-08-25T15:35:01Z
dc.date.issued 2011
dc.identifier 80054928981
dc.identifier.citation pagination=979-991; journalVolume=70; journalIssueNumber=11; journalTitle=JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3585
dc.identifier.uri doi:10.1097/NEN.0b013e318233afd7
dc.description.abstract Angiogenesis is believed to be essential for the growth of metastatic tumors in the brain. We analyzed the vascularization of tumors formed by 4 epithelial cell lines (C38, ZR75, HT25, and H1650) and a fibrosarcoma (HT1080) cell line injected into the brains of mice. No peritumoral angiogenesis was observed. Tumors apparently acquired their vasculature by incorporation of native vessels. Vessel density was lower, but vessel diameter and vascular cell proliferation were higher within all tumors versus those in the peritumoral tissue. There was an inverse correlation between the number of incorporated vessels and vascular cell proliferation. Epithelial tumors with pushing growth patterns had lower vessel density and elevated vascular cell proliferation compared with invasive tumors. The incorporated vessels retained their normal structure, with the exception of astrocyte foot processes that were replaced by tumor cells. Attachment to the vascular basement membrane led to the differentiation of the ZR75 breast cancer cells. In the HT1080 metastases, there was intussusceptive angiogenesis, that is, the fibrosarcoma cells that were attached to the vessel caused lumen splitting and filled the developing pillars. Branching angiogenesis was not observed either in the tumors or in control cerebral wounds. These data suggest that sprouting angiogenesis is not needed for the incipient growth of cerebral metastases and that tumor growth in this model is a result of incorporation of host vessels.
dc.relation.ispartof urn:issn:0022-3069
dc.title Lack of Angiogenesis in Experimental Brain Metastases
dc.type Journal Article
dc.date.updated 2016-06-16T11:17:54Z
dc.language.rfc3066 en
dc.identifier.mtmt 1756235
dc.identifier.wos 000296567800004
dc.identifier.pubmed 22002424
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.department SE/AOK/I/II. Sz. Patológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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