Journal
CANCER TREATMENT REVIEWS
Volume 32, Issue 4, Pages 261-276Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.ctrv.2006.03.004
Keywords
O-6-benzylguanine; chemotherapy; DNA repair; alkyltransferase; alkylation; platination
Categories
Funding
- NCI NIH HHS [CA81485] Funding Source: Medline
- NIGMS NIH HHS [5 T32 GM07281] Funding Source: Medline
- NATIONAL CANCER INSTITUTE [R01CA081485] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007281] Funding Source: NIH RePORTER
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DNA adducts at the O-6-position of guanine are a result of the carcinogenic, mutagenic and cytotoxic actions of methylating and chloroethylating agents. The presence of the DNA repair protein O-6-alkylguanine-DNA alkyltransferase (AGT) renders cells resistant to the biological effects induced by agents that attack at this position. O-6-Benzylguanine (O-6-BG) is a low molecular weight substrate of AGT and therefore, results in sensitizing cells and tumors to alkylating agent-induced cytotoxicity and antitumor activity. Presently, chemotherapy regimens of O-6-BG in combination with BCNU, temozolomide and Gliadel are in clinical development. Other ongoing clinical trials include expression of mutant AGT proteins that confer resistance to O-6-BG in bone marrow stem cells, in an effort to reduce the potential enhanced toxicity and mutagenicity of alkylating agents in the bone marrow. O-6-BG has also been found to enhance the cytotoxicity of agents that do not form adducts at the O-6-position of DNA, including platinating agents. O-6-BG's mechanism of action with these agents is not fully understood; however, it is independent of AGT activity or AGT inactivation. A better understanding of the effects of this agent will contribute to its clinical usefulness and the design of better analogs to further improve cancer chemotherapy. (c) 2006 Elsevier Ltd. All rights reserved.
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