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Cited by 539

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Inhibition of transcription by platinum antitumor compounds

Open access
Todd, Ryan C., Lippard, Stephen J.·2009·Metallomics

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. Platinum anticancer compounds bind to nuclear DNA, inhibit transcription, and induce apoptosis. Insight into the molecular mechanism of this process will aid researchers in the design of new metal-based chemotherapeutic agents.

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Crossref · 10.1039/b907567d

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Metadata

Authors
Todd, R. C., & Lippard, S. J.
Venue
Metallomics
Published
2009
Volume
1
Issue
4
Pages
280
ISSN
  • 1756-5901 (ISSN-L)
  • 1756-591X
OpenAlex
W2006826463
Cited by
539
References
3
FWCI
14.17
Type
journal article
Language
en
Open access
bronze

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