Role of MGMT,p53 and DSB Repair in Alkylating Drug-induced Apoptosis:Implications for Glioma Therapy

来源 :BIT Life Sciences' 1st Annual World Cancer Congess-2008( | 被引量 : 0次 | 上传用户:dingzhiyoulan
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  An important group of anticancer drugs are methylating and chloroethylating agents that are being used in first line therapy of gliomas and malignant melanomas.These agents induce a dozen of DNA lesions, some of them have been identified to be carcinogenic, genotoxic and cytotoxic.In MGMT lacking cells O6-methylguanine (O6MeG) and O6-chloroethylguanine (O6ChlG) are the major trigger of genotoxicity and apoptosis.In the case of O6MeG lesions, this requires MSH2/MSH6 dependent mismatch repair.O6MeG triggered cell death is regulated in a cell type specific manner, utilizing both the mitochondrial and the death receptor pathway.
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