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pubmed-article:18814044pubmed:abstractTextDevelopment of new therapies for glioblastoma requires animal models that mimic the biological characteristics of human brain tumors. On the other hand, potential antitumoral effects of a new therapeutic strategy are often established by evaluation of tumor cells apoptosis. Caspases are key mediators in the regulation and execution of apoptosis. Caspase-9 is activated during the intrinsic pathway downstream of mitochondria while caspase-3 is an effector caspase that initiates degradation of the cell in the final stages of apoptosis. Bax is a pro-apoptotic member of the Bcl-2 family that play key roles in the regulation of intrinsic apoptotic signaling. In the present study we investigated the immunohistochemical distribution of caspase 3, 9 and Bax in intracranial U87 glioblastoma xenograft. Immunohistochemistry showed that the glioblastoma xenografts contain cells positive for caspase-3, caspase-9, and Bax.lld:pubmed
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pubmed-article:18814044pubmed:articleTitleImmunohistochemical localization of caspase-3, caspase-9 and Bax in U87 glioblastoma xenografts.lld:pubmed
pubmed-article:18814044pubmed:affiliationDepartment of Animal Biology, Faculty of Biology, University of Bucharest, Splaiul Independentei 91-95, R-050095 Bucharest, Romania. otilia@bio.unibuc.rolld:pubmed
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