| Literature DB >> 20046924 |
Ryan C Todd1, Stephen J Lippard.
Abstract
Cisplatin, carboplatin, and oxaliplatin are three FDA-approved members of the platinum anticancer drug family. These compounds induce apoptosis in tumor cells by binding to nuclear DNA, forming a variety of structural adducts and triggering cellular responses, one of which is the inhibition of transcription. In this report we present (i) a detailed review of the structural investigations of various Pt-DNA adducts and the effects of these lesions on global DNA geometry; (ii) research detailing inhibition of cellular transcription by Pt-DNA adducts; and (iii) a mechanistic analysis of how DNA structural distortions induced by platinum damage may inhibit RNA synthesis in vivo. A thorough understanding of the molecular mechanism of action of platinum antitumor agents will aid in the development of new compounds in the family.Entities:
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Year: 2009 PMID: 20046924 PMCID: PMC2752884 DOI: 10.1039/b907567d
Source DB: PubMed Journal: Metallomics ISSN: 1756-5901 Impact factor: 4.526