Small molecule inhibitors of mammalian thioredoxin reductase

被引:146
作者
Cai, Wenqing [1 ]
Zhang, Liangwei [1 ]
Song, Yanlin [1 ]
Wang, Baolin [1 ]
Zhang, Baoxin [1 ]
Cui, Xuemei [1 ]
Hu, Guanming [1 ]
Liu, Yaping [1 ]
Wu, Jincai [1 ]
Fang, Jianguo [1 ]
机构
[1] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China
关键词
Thioredoxin; Redox; Cancer; Selenocysteine; CANCER-CELL GROWTH; IN-VITRO; RIBONUCLEOTIDE REDUCTASE; ANTICANCER ACTIVITY; CURCUMIN ANALOGS; ORGANOTELLURIUM COMPOUNDS; ORGANOGOLD(III) COMPOUNDS; GLUTATHIONE-REDUCTASE; GOLD(I) COMPLEXES; REDOX REGULATION;
D O I
10.1016/j.freeradbiomed.2011.10.447
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
Mammalian thioredoxin reductases (TrxRs) are a family of NADPH-dependent flavoproteins with a penultimate selenocysteine residue at the carboxy-terminus. Besides their native substrate thioredoxins (Trx), the enzymes show a broad substrate specificity, at least partially, because of the C-terminal redox-active site that is easily accessible in the reduced form. TrxRs are ubiquitous in all kinds of cells and have a critical role in regulating intracellular redox signaling. In recent years, a wealth of evidence has revealed that overactivation/dysfunction of TrxRs is closely related to various diseases, especially in tumor development, and thus the past decades have witnessed an expanding interest in finding TrxRs inhibitors, which might be promising agents for cancer chemotherapy. Herein we reviewed the small molecule inhibitors of mammalian TrxRs, with an emphasis on those that have potential anticancer activity. This review includes the nonpatent references up to 2010 that deal with mammalian TrxR inhibitors. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:257 / 265
页数:9
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