Abstract
MCF-7/AdrVp is a multidrug-resistant human breast cancer subline that displays an ATP-dependent reduction in the intracellular accumulation of anthracycline anticancer drugs in the absence of overexpression of known multidrug resistance transporters such as P glycoprotein or the multidrug resistance protein. RNA fingerprinting led to the identification of a 2.4-kb mRNA that is overexpressed in MCF-7/AdrVp cells relative to parental MCF-7 cells. The mRNA encodes a 655-aa [corrected] member of the ATP-binding cassette superfamily of transporters that we term breast cancer resistance protein (BCRP). Enforced expression of the full-length BCRP cDNA in MCF-7 breast cancer cells confers resistance to mitoxantrone, doxorubicin, and daunorubicin, reduces daunorubicin accumulation and retention, and causes an ATP-dependent enhancement of the efflux of rhodamine 123 in the cloned transfected cells. BCRP is a xenobiotic transporter that appears to play a major role in the multidrug resistance phenotype of MCF-7/AdrVp human breast cancer cells.
MeSH Terms
ATP Binding Cassette Transporter, Subfamily G, Member 2
ATP-Binding Cassette Transporters/biosynthesis,chemistry,genetics
Adenosine Triphosphate/metabolism
Amino Acid Sequence
Animals
Antineoplastic Agents/toxicity
Breast Neoplasms
Cell Survival/drug effects
Cloning, Molecular
DNA Primers
Daunorubicin/pharmacokinetics
Drug Resistance, Multiple
Female
Gene Library
Humans
Molecular Sequence Data
Neoplasm Proteins
Phylogeny
RNA, Messenger/genetics
Recombinant Proteins/biosynthesis,chemistry
Reverse Transcriptase Polymerase Chain Reaction
Software
Transcription, Genetic
Transfection
Tumor Cells, Cultured
Chemicals
ABCG2 protein, human
ATP Binding Cassette Transporter, Subfamily G, Member 2
ATP-Binding Cassette Transporters
Antineoplastic Agents
DNA Primers
Neoplasm Proteins
RNA, Messenger
Recombinant Proteins
Adenosine Triphosphate
Daunorubicin
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Doyle L A
Greenebaum Cancer Center of the University of Maryland, Baltimore MD 21201, USA.
Yang W
Abruzzo L V
Krogmann T
Gao Y
Rishi A K
Ross D D
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