Advances in the Molecular Detection of ABC Transporters Involved in Multidrug Resistance in Cancer

被引:65
作者
Gillet, Jean-Pierre [1 ]
Gottesman, Michael M. [1 ]
机构
[1] NCI, Cell Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
ABC transporters; clinical diagnosis; personalized medicine; TaqMan-based qRT-PCR; BINDING CASSETTE TRANSPORTERS; GENE-EXPRESSION ANALYSIS; DRUG TRANSPORTERS; MYELOID-LEUKEMIA; P-GLYCOPROTEIN; CELL-LINES; PROTEINS; MICROARRAY; PREDICTION; CHEMOSENSITIVITY;
D O I
10.2174/138920111795163931
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ATP-Binding Cassette (ABC) transporters are important mediators of multidrug resistance (MDR) in patients with cancer. Although their role in MDR has been extensively studied in vitro, their value in predicting response to chemotherapy has yet to be fully determined. Establishing a molecular diagnostic assay dedicated to the quantitation of ABC transporter genes is therefore critical to investigate their involvement in clinical MDR. In this article, we provide an overview of the methodologies that have been applied to analyze the mRNA expression levels of ABC transporters, by describing the technology, its pros and cons, and the experimental protocols that have been followed. We also discuss recent studies performed in our laboratory that assess the ability of the currently available high-throughput gene expression profiling platforms to discriminate between highly homologous genes. This work led to the conclusion that high-throughput TaqMan-based qRT-PCR platforms provide standardized clinical assays for the molecular detection of ABC transporters and other families of highly homologous MDR-linked genes encoding, for example, the uptake transporters (solute carriers-SLCs) and the phase I and II metabolism enzymes.
引用
收藏
页码:686 / 692
页数:7
相关论文
共 52 条
[1]   Analysis of ATP-binding cassette transporter expression in drug-selected cell lines by a microarray dedicated to multidrug resistance [J].
Annereau, JP ;
Szakacs, G ;
Tucker, CJ ;
Arciello, A ;
Cardarelli, C ;
Collins, J ;
Grissom, S ;
Zeeberg, BR ;
Reinhold, W ;
Weinstein, JN ;
Pommier, Y ;
Paules, RS ;
Gottesman, MM .
MOLECULAR PHARMACOLOGY, 2004, 66 (06) :1397-1405
[2]   Transport of lipids by ABC proteins: Interactions and implications for cellular toxicity, viability and function [J].
Aye, Irving L. M. H. ;
Singh, Ambika T. ;
Keelan, Jeffrey A. .
CHEMICO-BIOLOGICAL INTERACTIONS, 2009, 180 (03) :327-339
[3]  
Calcagno Anna Maria, 2007, Current Drug Delivery, V4, P324, DOI 10.2174/156720107782151241
[4]  
Cascorbi I, 2010, METHODS MOL BIOL, V596, P95, DOI 10.1007/978-1-60761-416-6_6
[5]   Intracellular ABC transporter A3 confers multidrug resistance in leukemia cells by lysosomal drug sequestration [J].
Chapuy, B. ;
Koch, R. ;
Radunski, U. ;
Corsham, S. ;
Cheong, N. ;
Inagaki, N. ;
Ban, N. ;
Wenzel, D. ;
Reinhardt, D. ;
Zapf, A. ;
Schweyer, S. ;
Kosari, F. ;
Klapper, W. ;
Truemper, L. ;
Wulf, G. G. .
LEUKEMIA, 2008, 22 (08) :1576-1586
[6]   ABC transporter A3 facilitates lysosomal sequestration of imatinib and modulates susceptibility of chronic myeloid leukemia cell lines to this drug [J].
Chapuy, Bjoern ;
Panse, Melanie ;
Radunski, Ulf ;
Koch, Raphael ;
Wenzel, Dirk ;
lnagaki, Nobuya ;
Haase, Detlef ;
Truemper, Lorenz ;
Wulf, Gerald G. .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 (11) :1528-1536
[7]   Genetics of ATP-binding cassette transporters [J].
Dean, M .
PHASE II CONJUGATION ENZYMES AND TRANSPORT SYSTEMS, 2005, 400 :409-429
[8]   Transmembrane transport of endo- and xenobiotics by mammalian ATP-binding cassette multidrug resistance proteins [J].
Deeley, Roger G. ;
Westlake, Christopher ;
Cole, Susan P. C. .
PHYSIOLOGICAL REVIEWS, 2006, 86 (03) :849-899
[9]  
Ding CM, 2009, METHODS MOL BIOL, V578, P245, DOI 10.1007/978-1-60327-411-1_16
[10]   The essential ATP-binding cassette protein RLI1 functions in translation by promoting preinitiation complex assembly [J].
Dong, JS ;
Lai, R ;
Nielsen, K ;
Fekete, CA ;
Qiu, HF ;
Hinnebusch, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (40) :42157-42168