BRCA1 down-regulates cellular levels of reactive oxygen species

被引:60
作者
Saha, Tapas [1 ]
Rih, Jeong Keun [1 ]
Rosen, Eliot M. [1 ,2 ,3 ]
机构
[1] Georgetown Univ, Dept Oncol, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[2] Georgetown Univ, Dept Radiat Med, Med Ctr, Washington, DC 20057 USA
[3] Georgetown Univ, Dept Biochem & Mol & Cellular Biol, Med Ctr, Washington, DC 20057 USA
来源
FEBS LETTERS | 2009年 / 583卷 / 09期
关键词
BRCA1; Reactive oxygen species (ROS); Nitrotyrosine; 8-Oxoguanine; REF1; Oxidative stress; OXIDATIVE STRESS; BREAST; PROTECTION; CELLS;
D O I
10.1016/j.febslet.2009.04.005
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
Previous studies have shown that the breast cancer suppressor BRCA1 stimulates antioxidant gene expression and protects cells against oxidative stress. To further examine this important function, we tested whether BRCA1 could modulate intracellular levels of reactive oxygen species (ROS). Wild-type BRCA1 (but not a cancer-associated mutant) significantly reduced ROS levels, determined by DCF fluorescence assays by flow cytometry and confocal microscopy. The BRCA1 and REF1 pathways for reduction of ROS levels appear to exhibit cross-talk. BRCA1 also reduced the levels of protein nitration and H2O2-induced oxidative damage to DNA. Thus, BRCA1 may protect cellular macromolecules by reducing intracellular ROS levels. (C) 2009 Published by Elsevier B. V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:1535 / 1543
页数:9
相关论文
共 15 条
[1]   BRCA1 induces antioxidant gene expression and resistance to oxidative stress [J].
Bae, I ;
Fan, S ;
Meng, QH ;
Rih, JK ;
Kim, HJ ;
Kang, HJ ;
Xu, JW ;
Goldberg, ID ;
Jaiswal, AK ;
Rosen, EM .
CANCER RESEARCH, 2004, 64 (21) :7893-7909
[2]   Absence of full-length Brca1 sensitizes mice to oxidative stress and carcinogen-induced tumorigenesis in the esophagus and forestomach [J].
Cao, Liu ;
Xu, Xiaoling ;
Cao, Longyue L. ;
Wang, Rui-Hong ;
Coumoul, Xavier ;
Kim, Sang S. ;
Deng, Chu-Xia .
CARCINOGENESIS, 2007, 28 (07) :1401-1407
[3]   BRCA1 and BRCA2 as molecular targets for phytochemicals indole-3-carbinol and genistein in breast and prostate cancer cells [J].
Fan, S ;
Meng, Q ;
Auborn, K ;
Carter, T ;
Rosen, EM .
BRITISH JOURNAL OF CANCER, 2006, 94 (03) :407-426
[4]   Mitochondrial thioltransferase (glutaredoxin 2) has GSH-dependent and thioredoxin reductase-dependent peroxidase activities in vitro and in lens epithelial cells [J].
Fernando, M. Rohan ;
Lechner, Joel M. ;
Lofgren, Stefan ;
Gladyshev, Vadim N. ;
Lou, Marjorie F. .
FASEB JOURNAL, 2006, 20 (14) :2645-+
[5]  
Fischer JL, 2006, ANTICANCER RES, V26, P899
[6]   APE/Ref-1 and the mammalian response to genotoxic stress [J].
Fritz, G ;
Grösch, S ;
Tomicic, M ;
Kaina, B .
TOXICOLOGY, 2003, 193 (1-2) :67-78
[7]   Healthy aging: regulation of the metabolome by cellular redox modulation and prooxidant signaling systems: The essential roles of superoxide anion and hydrogen peroxide [J].
Linnane, Anthony William ;
Kios, Michael ;
Vitetta, Luis .
BIOGERONTOLOGY, 2007, 8 (05) :445-467
[8]   Superoxide dismutase in aging and disease: An overview [J].
McCord, JM .
SUPEROXIDE DISMUTASE, 2002, 349 :331-341
[9]   A STRONG CANDIDATE FOR THE BREAST AND OVARIAN-CANCER SUSCEPTIBILITY GENE BRCA1 [J].
MIKI, Y ;
SWENSEN, J ;
SHATTUCKEIDENS, D ;
FUTREAL, PA ;
HARSHMAN, K ;
TAVTIGIAN, S ;
LIU, QY ;
COCHRAN, C ;
BENNETT, LM ;
DING, W ;
BELL, R ;
ROSENTHAL, J ;
HUSSEY, C ;
TRAN, T ;
MCCLURE, M ;
FRYE, C ;
HATTIER, T ;
PHELPS, R ;
HAUGENSTRANO, A ;
KATCHER, H ;
YAKUMO, K ;
GHOLAMI, Z ;
SHAFFER, D ;
STONE, S ;
BAYER, S ;
WRAY, C ;
BOGDEN, R ;
DAYANANTH, P ;
WARD, J ;
TONIN, P ;
NAROD, S ;
BRISTOW, PK ;
NORRIS, FH ;
HELVERING, L ;
MORRISON, P ;
ROSTECK, P ;
LAI, M ;
BARRETT, JC ;
LEWIS, C ;
NEUHAUSEN, S ;
CANNONALBRIGHT, L ;
GOLDGAR, D ;
WISEMAN, R ;
KAMB, A ;
SKOLNICK, MH .
SCIENCE, 1994, 266 (5182) :66-71
[10]   Biochemistry of protein tyrosine nitration in cardiovascular pathology [J].
Peluffo, Gonzalo ;
Radi, Rafael .
CARDIOVASCULAR RESEARCH, 2007, 75 (02) :291-302