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PMID: 8275468 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Overexpression of multidrug resistance-associated protein (MRP) increases resistance to natural product drugs.

Cancer research ·Vol. 54 ·No. 2 ·1994-01-15 ·Pages 357-61

Grant CE, Valdimarsson G, Hipfner DR, Almquist KC, Cole SP, Deeley RG

Abstract

Amplification of the gene encoding multidrug resistance-associated protein (MRP) and overexpression of its cognate mRNA have been detected in multidrug-resistant cell lines derived from several different tumor types. To establish whether or not the increase in MRP is responsible for drug resistance in these cell lines, we have transfected HeLa cells with MRP expression vectors. The transfectants display an increase in resistance to doxorubicin that is proportional to the levels of a M(r) 190,000, integral membrane protein recognized by anti-MRP antibodies. The transfectants are also resistant to vincristine and VP-16 but not to cisplatin. The results demonstrate that MRP overexpression confers a multidrug resistance phenotype similar to that formerly associated exclusively with elevated levels of P-glycoprotein.

MeSH Terms
Carcinoma, Small Cell/genetics,metabolism Doxorubicin/pharmacology Drug Resistance/genetics,physiology Gene Amplification/genetics HeLa Cells Humans Lung Neoplasms/genetics,metabolism Neoplasm Proteins/chemistry,genetics Phenotype RNA, Messenger/analysis RNA, Neoplasm/analysis Transfection Tumor Cells, Cultured
Chemicals
Neoplasm Proteins RNA, Messenger RNA, Neoplasm Doxorubicin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Grant C E
Cancer Research Laboratories, Queen's University, Kingston, Ontario, Canada.
Valdimarsson G
Hipfner D R
Almquist K C
Cole S P
Deeley R G
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1994-01-15
Pages
357-61
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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