P-glycloprotein: So many ways to turn it on

被引:99
作者
Callaghan, Richard [1 ]
Crowley, Emily [1 ]
Potter, Simon [2 ]
Kerr, Ian D. [2 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Lab Sci, Oxford OX3 9DU, England
[2] Univ Nottingham, Sch Biomed Sci, Queens Med Ctr, Nottingham NG7 2RD, England
基金
英国医学研究理事会;
关键词
P-glycoprotem; ABCB1; drug resistance; chemotherapy; drug elimination; drug absoiption;
D O I
10.1177/0091270007311568
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Expression of the ABC transporter P-glycoprotein (P-gp or ABCB1) is associated with resistance to chemotherapy in cancer. However, early investigations into the regulation of ABCB1 expression revealed that the process is not a classical induction as observed for certain metabolizing enzymes. The process involves the cellular stress response pathway initiated by either inflicted (eg, chemotherapy damage) or endogenous (eg, hypoxia) factors, However, ABCB1 is also expressed in a number of noncancerous tissues. In particular, the protein is found at tissues providing a barrier or secretory function. The localization of ABCB1 in normal tissues will impact significantly on drug pharmacokinetics, in particular the absorption and elimination processes. This review also describes the mechanism underlying ABCB1 expression in noncancerous tissue, a process that does not involve the stress response.
引用
收藏
页码:365 / 378
页数:14
相关论文
共 158 条
[11]  
Brown NS, 2000, CANCER RES, V60, P6298
[12]   COINDUCTION OF MDR-1 MULTIDRUG-RESISTANCE AND CYTOCHROME-P-450 GENES IN RAT-LIVER BY XENOBIOTICS [J].
BURT, RK ;
THORGEIRSSON, SS .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (17) :1383-1386
[13]   The translocation mechanism of P-glycoprotein [J].
Callaghan, R ;
Ford, RC ;
Kerr, ID .
FEBS LETTERS, 2006, 580 (04) :1056-1063
[14]   INDUCTION OF MULTIDRUG RESISTANCE IN HUMAN-CELLS BY TRANSIENT EXPOSURE TO DIFFERENT CHEMOTHERAPEUTIC DRUGS [J].
CHAUDHARY, PM ;
RONINSON, IB .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (08) :632-639
[15]  
Chen WL, 2001, J LIPID RES, V42, P1402
[16]   Organ distribution of multidrug resistance proteins 1, 2, and 3 (Mrp1, 2, and 3) rnRNA and hepatic induction of mrp3 by constitutive androstane receptor activators in rats [J].
Cherrington, NJ ;
Hartley, DP ;
Li, N ;
Johnson, DR ;
Klaassen, CD .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 300 (01) :97-104
[17]  
CHIN KV, 1990, J BIOL CHEM, V265, P221
[18]   OVEREXPRESSION OF A TRANSPORTER GENE IN A MULTIDRUG-RESISTANT HUMAN LUNG-CANCER CELL-LINE [J].
COLE, SPC ;
BHARDWAJ, G ;
GERLACH, JH ;
MACKIE, JE ;
GRANT, CE ;
ALMQUIST, KC ;
STEWART, AJ ;
KURZ, EU ;
DUNCAN, AMV ;
DEELEY, RG .
SCIENCE, 1992, 258 (5088) :1650-1654
[19]   c-Jun NH2-terminal kinase activation contributes to hypoxia-inducible factor 1α-dependent P-glycoprotein expression in hypoxia [J].
Comerford, KM ;
Cummins, EP ;
Taylor, CT .
CANCER RESEARCH, 2004, 64 (24) :9057-9061
[20]  
Comerford KM, 2002, CANCER RES, V62, P3387