[Advances in the study of expression and regulation of P-glycoprotein]

Yao Xue Xue Bao. 2007 Sep;42(9):911-6.
[Article in Chinese]

Abstract

Resistance to the cytotoxic actions of antineoplastic drugs remains a barrier to the establishment of curative chemotherapy regimens for cancer. Over-expression of P-glycoprotein (P-gp), encoded by the MDR1 gene is the major molecular mechanism enhancing efflux pump for various anticancer agents, hence caused MDR. Transcription factor, DNA methylation, histone acetylation/deacetylation, phosphorylation and glycosylation and MDR1 gene polymorphisms play pivotal role in regulation of P-glycoprotein, and may become new therapeutic targets. This paper summarized the advances of studies on expression and regulation of P-glycoprotein.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Acetylation
  • DNA Methylation
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Gene Expression Regulation, Neoplastic
  • Genes, MDR*
  • Glycosylation
  • Humans
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Phosphorylation
  • Polymorphism, Genetic*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Transcription Factors