Alkylating agents are the most widely used anticancer drugs whose main target is the DNA, although how exactly the DNA lesions cause cell death is still not clear. The emergence of resistance to this class of drugs as well as to other antitumor agents is one of the major causes of failure of cancer treatment. This paper reviews some of the best characterized mechanisms of resistance to alkylating agents. Pre- and post-target mechanisms are recognized, the former able to limit the formation of lethal DNA adducts, and the latter enabling the cell to repair or tolerate the damage. The role in the pre-target mechanisms of reduced drug accumulation and the increased detoxification or activation systems (such as DT-diaphorase, metallothionein, GST/GSH system, etc...) are discussed. In the post-target mechanisms the different DNA repair pathways, tolerance to alkylation damage and the ‘downstream’ effects (cell cycle arrest and/or apoptosis) are examined.
机构:
Mayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
Mayo Clin, Dept Pathol, Rochester, MN 55905 USAMayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
Sarkaria, Jann N.
Kitange, Gaspar J.
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Mayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
Mayo Clin, Dept Pathol, Rochester, MN 55905 USAMayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
Kitange, Gaspar J.
James, C. David
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Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
Univ Calif San Francisco, Brain Tumor Res Ctr, San Francisco, CA 94143 USAMayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
James, C. David
Plummer, Ruth
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Univ Newcastle Upon Tyne, No Inst Canc Res, Newcastle, EnglandMayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA
Plummer, Ruth
Calvert, Hilary
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Univ Newcastle Upon Tyne, No Inst Canc Res, Newcastle, EnglandMayo Clin, Dept Radiat Oncol, Rochester, MN 55905 USA