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Breast cancer resistance protein (BCRP/ABCG2).

Abstract
Breast cancer resistance protein (BCRP) was identified 7 years ago as the most recent member of ABC drug efflux membrane transporters. It is a 655 amino acid peptide with an ability to extrude a wide variety of chemical compounds from the cells. Today, it is considered as one of three major transporters causing drug resistance in mammalian cells. It is also distributed in epithelia involved in drug disposition with major role in the placenta, liver and intestine. In addition, BCRP is responsible for the "side population" phenotype of stem cells and seems to play a significant role in protection against hypoxia. BCRP inhibitors are currently searched for to overcome drug resistance and to improve the pharmacokinetics, mainly intestinal absorption, of substrate drugs. Mutant BCRP has also been used as a selectable marker in stem cell gene therapy applications.
AuthorsFrantisek Staud, Petr Pavek
JournalThe international journal of biochemistry & cell biology (Int J Biochem Cell Biol) Vol. 37 Issue 4 Pg. 720-5 (Apr 2005) ISSN: 1357-2725 [Print] Netherlands
PMID15694832 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • ABCG2 protein, human
  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters
  • Neoplasm Proteins
Topics
  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters (chemistry, metabolism, physiology)
  • Humans
  • Mutation
  • Neoplasm Proteins (chemistry, metabolism, physiology)
  • Polymorphism, Single Nucleotide

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