Multidrug Resistance Through the Spectacle of P-Glycoprotein

被引:100
作者
Goda, Katalin [1 ]
Bacso, Zsolt [1 ]
Szabo, Gabor [1 ]
机构
[1] Univ Debrecen, Dept Biophys & Cell Biol, Med & Hlth Sci Ctr, H-4012 Debrecen, Hungary
关键词
P-glycoprotein; multidrug resistance; hydrophobicity; membrane microdomains; BINDING CASSETTE TRANSPORTERS; REFRACTORY MULTIPLE-MYELOMA; MEDIATED DRUG-RESISTANCE; HIGH-AFFINITY BINDING; BLOOD-BRAIN-BARRIER; LIPID RAFTS; CANCER-CELLS; ATPASE ACTIVITY; ABC TRANSPORTERS; PLASMA-MEMBRANE;
D O I
10.2174/156800909788166493
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:281 / 297
页数:17
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