Transcriptional regulators of the human multidrug resistance 1 gene: recent views

被引:141
作者
Labialle, S
Gayet, L
Marthinet, E
Rigal, D
Baggetto, LG
机构
[1] UCBL, CNRS, UMR 5086, IBCP, F-69367 Lyon 07, France
[2] EFS Lyon, F-69007 Lyon, France
关键词
hMDR1; gene; multidrug resistance; P-glycoprotein; transcriptional regulation;
D O I
10.1016/S0006-2952(02)01156-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The multidrug resistance (MDR) phenotype is the major cause of failure of cancer chemotherapy. This phenotype is mainly due to the overexpression of the human MDR1 (hMDR1) gene. Several studies have shown that transcriptional regulation of this gene is unexpectedly complex and is far from being completely understood. Current work is aimed mainly at defining unclear and new control regions in the hMDR1 gene promoter as well as clarifying corresponding signaling pathways. Such studies provide new insights into the mechanisms by which xenobiotic molecules might modify the physiological hMDR1 expression as well as the possible role of oncogenes in the pathological dysregulation of the gene. Here we report recent findings on the regulation of hMDR1 which may help define specific targets aimed at modulating its transcription. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:943 / 948
页数:6
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