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pubmed-article:11949826pubmed:abstractTextRadiotherapy is the standard treatment for glioblastoma. Here, we assessed the radiosensitivity of 12 human malignant glioma cell lines in vitro and correlated these data with irradiation-induced cell cycle changes, chemosensitivity profiles and BCL-2 family protein expression. Irradiation at 3 Gy failed to cause major cell cycle perturbations. Radioresistance was associated with collateral sensitivity to the topoisomerase II inhibitors, teniposide and doxorubicin. High levels of BCL-XL and low levels of BAX were independently linked to radioresistance. Ectopic expression of a BAX transgene induced radiosensitization in the LN-18 cell line. Thus, BCL-2 family protein expression modulates radiosensitivity in human glioma cells and targeted alterations in BCL-2 family protein expression are a promising strategy to improve the therapeutic efficacy of radiotherapy for gliomas.lld:pubmed
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pubmed-article:11949826pubmed:pagination43-9lld:pubmed
pubmed-article:11949826pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11949826pubmed:articleTitleBCL-2 family proteins modulate radiosensitivity in human malignant glioma cells.lld:pubmed
pubmed-article:11949826pubmed:affiliationDepartment of Neurology, University of Tübingen, Germany.lld:pubmed
pubmed-article:11949826pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11949826pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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