Thioredoxin and thioredoxin-binding protein-2 in cancer and metabolic syndrome

被引:187
作者
Kaimul, Ahsan M.
Nakamura, Hajime
Masutani, Hiroshi
Yodoi, Junji
机构
[1] Kyoto Univ, Dept Biol Responses, Inst Virus Res, Lab Infect & Prevent,Sakyo Ku, Kyoto 6068507, Japan
[2] Kyoto Univ Hosp, Translat Res Ctr, Dept Expt Therapeut, Thioredoxin Project, Kyoto 6068507, Japan
基金
日本学术振兴会;
关键词
thioredoxin; redox; antioxidant; thioredoxin-binding protein-2; cancer; metabolism; free radicals;
D O I
10.1016/j.freeradbiomed.2007.05.032
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Thioredoxin (TRX), a small redox-active multifunctional protein, acts as a potent antioxidant and a redox regulator in signal transduction. TRX expression is elevated in various types of human cancer. Overexpression of TRX introduces resistance to anti-cancer drugs or radiation-induced apoptosis; however, there is no evidence that the incidence of cancer is frequent in TRX-transgenic mice or that the administration of recombinant human TRX enhances tumor growth. Plasma/serum level of TRX is a good marker for oxidative stress-induced various disorders, including metabolic syndrome. Thioredoxin-binding protem-2 (TBP-2), which was originally identified as a negative regulator of TRX, acts as a growth suppressor and a regulator in lipid metabolism. TBP-2 expression is downregulated in various types of human cancer. TBP-2 deficiency induces lipid dysfunction and a phenotype resembling Reye syndrome. Thus, TRX and TBP-2 play important roles in the pathophysiology of cancer and metabolic syndrome by direct interaction or by independent mechanisms. (c) 2007 Published by Elsevier Inc.
引用
收藏
页码:861 / 868
页数:8
相关论文
共 105 条
[1]
Loss of interleukin-2-dependency in HTLV-I-infected T cells on gene silencing of thioredoxin-binding protein-2 [J].
Ahsan, MK ;
Masutani, H ;
Yamaguchi, Y ;
Kim, YC ;
Nosaka, K ;
Matsuoka, M ;
Nishinaka, Y ;
Maeda, M ;
Yodoi, J .
ONCOGENE, 2006, 25 (15) :2181-2191
[2]
Thioredoxin-1 suppresses lung injury and apoptosis induced by diesel exhaust particles (DEP) by scavenging reactive oxygen species and by inhibiting DEP-induced downregulation of Akt [J].
Ahsan, MK ;
Nakamura, H ;
Tanito, M ;
Yamada, K ;
Utsumi, H ;
Yodoi, J .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 39 (12) :1549-1559
[3]
Human thioredoxin homodimers: Regulation by pH, role of aspartate 60, and crystal structure of the aspartate 60->asparagine mutant [J].
Andersen, JF ;
Sanders, DAR ;
Gasdaska, JR ;
Weichsel, A ;
Powis, G ;
Montfort, WR .
BIOCHEMISTRY, 1997, 36 (46) :13979-13988
[4]
The antitumor thioredoxin-1 inhibitor PX-12 (1-methylpropyl 2-imidazolyl disulfide) decreases thioredoxin-1 and VEGF levels in cancer patient plasma [J].
Baker, AF ;
Dragovich, T ;
Tate, WR ;
Ramanathan, RK ;
Roe, D ;
Hsu, CH ;
Kirkpatrick, DL ;
Powis, G .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2006, 147 (02) :83-90
[5]
Berggren M, 1996, ANTICANCER RES, V16, P3459
[6]
BJORNSTEDT M, 1994, J BIOL CHEM, V269, P29382
[7]
Positional cloning of the combined hyperlipidemia gene Hyplip1 [J].
Bodnar, JS ;
Chatterjee, A ;
Castellani, LW ;
Ross, DA ;
Ohmen, J ;
Cavalcoli, J ;
Wu, CY ;
Dains, KM ;
Catanese, J ;
Chu, M ;
Sheth, SS ;
Charugundla, K ;
Demant, P ;
West, DB ;
de Jong, P ;
Lusis, AJ .
NATURE GENETICS, 2002, 30 (01) :110-116
[8]
Thioredoxin: friend or foe in human disease? [J].
Burke-Gaffney, A ;
Callister, MEJ ;
Nakamura, H .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2005, 26 (08) :398-404
[9]
The histone deacetylase inhibitor SAHA arrests cancer cell growth, up-regulates thioredoxin-binding protein-2, and down-regulates thioredoxin [J].
Butler, LM ;
Zhou, XB ;
Xu, WS ;
Scher, HI ;
Rifkind, RA ;
Marks, PA ;
Richon, VM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (18) :11700-11705
[10]
Exenatide inhibits β-cell apoptosis by decreasing thioredoxin-interacting protein [J].
Chen, Junqin ;
Couto, Francesca M. ;
Minn, Alexandra H. ;
Shalev, Anath .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 346 (03) :1067-1074