Abstract
The overexpression of a plasma membrane glycoprotein, P-glycoprotein, is strongly correlated with the expression of multidrug resistance. This phenotype (frequently observed in cell lines selected for resistance to a single drug) is characterized by cross resistance to many drugs, some of which are used in cancer chemotherapy. In the present study we showed that DNA-mediated transformants of mouse LTA cells with DNA from multidrug-resistant hamster cells acquired the multidrug resistance phenotype, that the transformants contained hamster P-glycoprotein DNA sequences, that these sequences were amplified whereas the recipient mouse P-glycoprotein sequences remained at wild-type levels, and that the overexpressed P-glycoprotein in these cells was of hamster origin. Furthermore, we showed that the hamster P-glycoprotein sequences were transfected independently of a group of genes that were originally coamplified and linked within a 1-megabase-pair region in the donor hamster genome. These data indicate that the high expression of P-glycoprotein is the only alteration required to mediate multidrug resistance.
MeSH Terms
ATP Binding Cassette Transporter, Subfamily B, Member 1
Animals
Carrier Proteins/genetics
Cricetinae
Drug Resistance
Gene Amplification
Gene Expression Regulation
Glycoproteins/genetics,metabolism
Immunosorbent Techniques
Membrane Proteins/genetics
Mice
Transformation, Genetic
Chemicals
ATP Binding Cassette Transporter, Subfamily B, Member 1
Carrier Proteins
Glycoproteins
Membrane Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Deuchars K L
Du R P
Naik M
Evernden-Porelle D
Kartner N
van der Bliek A M
Ling V
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