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PMID: 9657519 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Proteins that specifically recognize cisplatin-damaged DNA: a clue to anticancer activity of cisplatin.

Zlatanova J, Yaneva J, Leuba SH

Abstract

Cisplatin, but not its trans geometric isomer, is a potent anticancer drug whose biological activity is a consequence of the formation of covalent adducts between the platinum compound and certain bases in DNA. Two classes of proteins have recently been identified that bind preferentially to damaged sites: proteins that specifically recognize those sites as a first step in their repair, and those that bind to such sites by virtue of structural similarity between the modified DNA and their own natural binding sites. Both classes of proteins may be involved, perhaps in opposing ways, in the cytotoxic effect of the drug.

MeSH Terms
Antineoplastic Agents/pharmacology Binding Sites Cisplatin/pharmacology DNA/drug effects DNA Adducts DNA Damage DNA Ligases/metabolism DNA Repair/drug effects DNA Replication/drug effects High Mobility Group Proteins/metabolism Humans
Chemicals
Antineoplastic Agents DNA Adducts High Mobility Group Proteins cisplatin-DNA adduct transplatin DNA DNA Ligases Cisplatin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Zlatanova J
Department of Biochemistry and Biophysics, Oregon State University, Corvallis 97331-7305, USA.
Yaneva J
Leuba S H
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
0892-6638
Published
1998-07-00
Pages
791-9
Language
English
Region
United States
NLM ID
8804484
Subset
IM
Grants
NIGMS NIH HHS · GM50276 · United States
FIC NIH HHS · TW00568-02 · United States
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