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PMID: 12429734 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cisplatin sensitivity in Hmbg1-/- and Hmbg1+/+ mouse cells.

The Journal of biological chemistry ·Vol. 278 ·No. 3 ·2003-01-17 ·Pages 1769-73

Wei M, Burenkova O, Lippard SJ

Abstract

The study presented here investigates the effect of HMGB1 knockout on the sensitivity of mouse embryonic fibroblasts treated with the anticancer drug cisplatin. We evaluated both the growth inhibition by cisplatin and cisplatin-induced cell death in the Hmgb1(-/-) cells and its wild-type counterpart. No significant differences were observed in the responses of these cells to cisplatin, indicating that HMGB1 does not play a significant role in modulating the cellular responses to cisplatin in this context. Since HMGB1 significantly enhances the cytotoxicity of cisplatin in other cells, these results illustrate the importance of cell type in determining the ability of this and probably other cisplatin-DNA-binding proteins to influence the efficacy of the drug.

MeSH Terms
Animals Antineoplastic Agents/pharmacology Cell Line Cisplatin/pharmacology HMGB1 Protein/genetics Mice Mice, Knockout
Chemicals
Antineoplastic Agents HMGB1 Protein Cisplatin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wei Min
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Burenkova Olga
Lippard Stephen J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2003-01-17
Epub
2002-00-11
Pages
1769-73
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA34992 · United States
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