4.4 Review

Multidrug Resistance Through the Spectacle of P-Glycoprotein

期刊

CURRENT CANCER DRUG TARGETS
卷 9, 期 3, 页码 281-297

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/156800909788166493

关键词

P-glycoprotein; multidrug resistance; hydrophobicity; membrane microdomains

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资金

  1. OTKA [TO46945, TO48742, K72762, PD 75994]
  2. Ministry of Public Health [ETT 067/2006]

向作者/读者索取更多资源

P-glycoprotein (Pgp), coded for by the mdr1 gene, is one of the ABC transporters held responsible for the phenomenon of multidrug resistance (mdr), which is reflected by a rapidly escalating failure of chemotherapy with different classes of cytotoxic agents: anthracyclins, vinca alkaloids, taxanes, epipodophylotoxins. Although overcoming resistance conveyed by Pgp alone may not be sufficient for reaching effective treatment, the abundance of observations available for this paradigmatic multidrug transporter at both in vitro and in vivo setting is a tempting ground for an updated assessment of the main currents of mdr research. In this review we attempt to help keep track of the features of Pgp-mediated drug transport that serve as the major starting points for ongoing efforts of mdr reversal. We will analyze the slowly narrowing gaps that prevail between our ever increasing understanding at the protein, cell and organism level, focusing on the molecular interactions involving Pgp.

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