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PMID: 3022150 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Isolation and expression of a complementary DNA that confers multidrug resistance.

Nature ·Vol. 323 ·No. 6090 ·1986-00-00 ·Pages 728-31

Gros P, Ben Neriah YB, Croop JM, Housman DE

Abstract

The emergence and outgrowth of a population of tumour cells resistant to multiple drugs is a major problem in the chemotherapeutic treatment of cancer. We have used highly drug-resistant cell lines developed in vitro to study the molecular basis of multidrug resistance. In these cell lines high levels of resistance are frequently associated with amplification and overexpression of a small group of genes termed mdr or gp170. Direct evaluation of the role of these genes in multidrug resistance has awaited the isolation of a member of this gene family in a biologically active form. Here we report the isolation of DNA clones complementary to the cellular messenger RNA transcripts of mdr genes and show that high-level expression of a full-length complementary DNA clone in an otherwise drug-sensitive cell confers a complete multidrug-resistant phenotype. Our results demonstrate that overexpression of a single member of the mdr group is sufficient to confer drug resistance. Furthermore, because the cDNA was isolated from a drug-sensitive cell, mutations in the primary sequence of mdr are not required to produce a multidrug-resistance phenotype.

MeSH Terms
Animals Base Sequence Cell Line Cricetinae DNA/isolation & purification DNA Restriction Enzymes/metabolism Drug Resistance/genetics Gene Expression Regulation Globins/genetics Phenotype RNA, Messenger/metabolism Transfection
Chemicals
RNA, Messenger Globins DNA DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Gros P
Ben Neriah Y B
Croop J M
Housman D E
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1986-00-00
Pages
728-31
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NHLBI NIH HHS · 5T 32HL07574 · United States
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