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pubmed-article:9623977pubmed:abstractTextThe transfer of apoptosis genes to tumors is one of the most promising strategies for cancer gene therapy. We have shown that massive apoptosis occurs when wild-type p53 expression is induced in glioma cells carrying a p53 gene mutation. However, adenovirus-mediated p53 gene transfer is ineffective in causing apoptosis in glioma cells that retain a wild-type p53 genotype. We evaluated the effect of E2F-1 overexpression on the growth of gliomas in vitro and in vivo. In the in vitro study, the adenovirus-mediated transfer of exogenous E2F-1 protein precipitated generalized apoptosis in gliomas. The treatment with Ad5CMV-E2F-1 of nude mice carrying subcutaneous gliomas arrested tumor growth. Our results indicate that E2F-1 has anti-glioma activity in vitro and in vivo.lld:pubmed
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pubmed-article:9623977pubmed:articleTitleOverexpression of E2F-1 in glioma triggers apoptosis and suppresses tumor growth in vitro and in vivo.lld:pubmed
pubmed-article:9623977pubmed:affiliationDepartment of Neuro-Oncology, The University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.lld:pubmed
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