Role of thioredoxin in cell growth through interactions with signaling molecules

被引:92
作者
Yoshioka, Jun [1 ]
Schreiter, Eric R. [1 ]
Lee, Richard T. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Cardiovasc Div, Boston, MA 02115 USA
关键词
D O I
10.1089/ars.2006.8.2143
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
The thioredoxin system helps maintain a reducing environment in cells, but thioredoxin functions as more than simply an antioxidant. Thioredoxin functions depend on the protein's redox state, as determined by two conserved cysteines. Key biologic activities of thioredoxin include antioxidant, growth control, and antiapoptotic properties, resulting from interaction with target molecules including transcription factors. Mechanisms by which thioredoxin regulates cell growth include binding to signaling molecules such as apoptosis signal-regulating kinase-1 (ASK-1) and thioredoxin-interacting protein (Txnip). The molecular interplay between thioredoxin, ASK-1, and Txnip potentially influences cell growth and survival in diverse human diseases such as cancer, diabetes, and heart disease. In this review, we focus on the structure of thioredoxin and its functional regulation of cell growth through the interactions with signaling molecules.
引用
收藏
页码:2143 / 2151
页数:9
相关论文
共 88 条
[11]  
ERICSON ML, 1992, LYMPHOKINE CYTOK RES, V11, P201
[12]  
FILBY CE, 2005, AM J PHYSL LUNG CELL
[13]  
FUJII S, 1991, CANCER, V68, P1583, DOI 10.1002/1097-0142(19911001)68:7<1583::AID-CNCR2820680720>3.0.CO
[14]  
2-N
[15]  
Gallegos A, 1996, CANCER RES, V56, P5765
[16]  
GASDASKA JR, 1995, CELL GROWTH DIFFER, V6, P1643
[17]   Oxidative inactivation of thioredoxin as a cellular growth factor and protection by a Cys(73)->Ser mutation [J].
Gasdaska, JR ;
Kirkpatrick, DL ;
Montfort, W ;
Kuperus, M ;
Hill, SR ;
Berggren, M ;
Powis, G .
BIOCHEMICAL PHARMACOLOGY, 1996, 52 (11) :1741-1747
[18]  
Goldberg SF, 2003, CANCER RES, V63, P432
[19]   Reactive oxygen species- and dimerization-induced activation of apoptosis signal-regulating kinase 1 in tumor necrosis factor-α signal transduction [J].
Gotoh, Y ;
Cooper, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) :17477-17482
[20]   ESPript:: analysis of multiple sequence alignments in PostScript [J].
Gouet, P ;
Courcelle, E ;
Stuart, DI ;
Métoz, F .
BIOINFORMATICS, 1999, 15 (04) :305-308