Glutathione transferases and development of new principles to overcome drug resistance

被引:239
作者
Sau, Andrea [1 ]
Tregno, Francesca Pellizzari [1 ]
Valentino, Francesco [1 ]
Federici, Giorgio [2 ,3 ]
Caccuri, Anna Maria [1 ]
机构
[1] Univ Roma Tor Vergata, Dept Chem Sci & Technol, I-00133 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Internal Med, Rome, Italy
[3] Childrens Hosp, Ist Ricovero & Cura Carattere Sci Bambin Gesua, Rome, Italy
关键词
GST; MDR; MAPK; Pro-drug; Inhibitor; S-TRANSFERASE; MULTIDRUG-RESISTANCE; PROTEIN-1; MRP1; 6-(7-NITRO-2,1,3-BENZOXADIAZOL-4-YLTHIO)HEXANOL NBDHEX; CELL-LINE; IN-VITRO; C-JUN; CONJUGATION; SENSITIVITY; EXPRESSION;
D O I
10.1016/j.abb.2010.05.012
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
Chemoresistance is a multifactorial phenomenon and many studies clearly show that a coordinated expression of efflux transporter proteins and phase II conjugating enzymes in tumor cells is linked to the development of the multidrug resistance phenotype. In particular, the overexpression of glutathione S-transferases and efflux pumps in tumors may reduce the reactivity of various anticancer drugs. In recent years it has become evident that glutathione S-transferases are also involved in the control of apoptosis through the inhibition of the JNK signaling pathway. As such, the glutathione S-transferase superfamily has become the focus of extensive pharmaceutical research in attempt to generate more efficient anticancer agents. Here we present an overview of the GST inhibitors and the GST-activated pro-drugs utilized to date to overcome drug resistance. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:116 / 122
页数:7
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