Impaired OXPHOS Complex III in Breast Cancer

被引:86
作者
Owens, Kjerstin M. [1 ]
Kulawiec, Mariola [2 ]
Desouki, Mohamad Mokhtar [3 ]
Vanniarajan, Ayyasamy [1 ]
Singh, Keshav K. [1 ,4 ,5 ]
机构
[1] Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USA
[2] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[3] Med Univ S Carolina, Dept Pathol & Lab Med, Charleston, SC 29425 USA
[4] Univ Alabama Birmingham, Dept Pathol, Ctr Free Radical Biol, Dept Environm Hlth,Dept Genet,Ctr Aging, Birmingham, AL 35294 USA
[5] Univ Alabama Birmingham, UAB Comprehens Canc Ctr, Birmingham, AL USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION SIGNATURE; CYTOCHROME-C REDUCTASE; IRON-SULFUR CLUSTER; REACTIVE OXYGEN; OXIDATIVE-PHOSPHORYLATION; CELL MITOCHONDRIA; BC(1) COMPLEX; NADPH OXIDASE; PROTEIN; ROS;
D O I
10.1371/journal.pone.0023846
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
We measured the mitochondrial oxidative phosphorylation (mtOXPHOS) activities of all five complexes and determined the activity and gene expression in detail of the Complex III subunits in human breast cancer cell lines and primary tumors. Our analysis revealed dramatic differences in activity of complex III between normal and aggressive metastatic breast cancer cell lines. Determination of Complex III subunit gene expression identified over expression and co-regulation of UQCRFS1 (encoding RISP protein) and UQCRH (encoding Hinge protein) in 6 out of 9 human breast tumors. Analyses of UQCRFS1/RISP expression in additional matched normal and breast tumors demonstrated an over expression in 14 out of 40 (35%) breast tumors. UQCRFS1/RISP knockdown in breast tumor cell line led to decreased mitochondrial membrane potential as well as a decrease in matrigel invasion. Furthermore, reduced matrigel invasion was mediated by reduced ROS levels coinciding with decreased expression of NADPH oxidase 2, 3, 4 and 5 involved in ROS production. These studies provide direct evidence for contribution of impaired mtOXPHOS Complex III to breast tumorigenesis.
引用
收藏
页数:10
相关论文
共 38 条
[1]
[Anonymous], 1924, Biochem Z
[2]
The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313
[3]
AN EVALUATION OF THE MEASUREMENT OF THE ACTIVITIES OF COMPLEXES I-IV IN THE RESPIRATORY-CHAIN OF HUMAN SKELETAL-MUSCLE MITOCHONDRIA [J].
BIRCHMACHIN, MA ;
BRIGGS, HL ;
SABORIDO, AA ;
BINDOFF, LA ;
TURNBULL, DM .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1994, 51 (01) :35-42
[4]
Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation [J].
Brunelle, JK ;
Bell, EL ;
Quesada, NM ;
Vercauteren, K ;
Tiranti, V ;
Zeviani, M ;
Scarpulla, RC ;
Chandel, NS .
CELL METABOLISM, 2005, 1 (06) :409-414
[5]
Functional F1-ATPase essential in maintaining growth and membrane potential of human mitochondrial DNA-depleted ρ° cells [J].
Buchet, K ;
Godinot, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (36) :22983-22989
[6]
Cross talk between mitochondria and superoxide generating NADPH oxidase in breast and ovarian tumors [J].
Desouki, MM ;
Kulawiec, M ;
Bansal, S ;
Das, G ;
Singh, KK .
CANCER BIOLOGY & THERAPY, 2005, 4 (12) :1367-1373
[7]
Redox signalling involving NADPH oxidase-derived reactive oxygen species [J].
Dworakowski, R. ;
Anilkumar, N. ;
Zhang, M. ;
Shah, A. M. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2006, 34 :960-964
[8]
Gene expression in the urinary bladder:: A common carcinoma in situ gene expression signature exists disregarding histopathological classification [J].
Dyrskjot, L ;
Kruhoffer, M ;
Thykjaer, T ;
Marcussen, N ;
Jensen, JL ;
Moller, K ;
Orntoft, TF .
CANCER RESEARCH, 2004, 64 (11) :4040-4048
[9]
NADPH oxidase 4 is an oncoprotein localized to mitochondria [J].
Graham, Kelly A. ;
Kulawiec, Mariola ;
Owens, Kjerstin M. ;
Li, Xiurong ;
Desouki, Mohamed Mokhtar ;
Chandra, Dhyan ;
Singh, Keshav K. .
CANCER BIOLOGY & THERAPY, 2010, 10 (03) :223-231
[10]
The iron-sulfur cluster of the Rieske iron-sulfur protein functions as a proton-exiting gate in the cytochrome bc1 complex [J].
Gurung, B ;
Yu, L ;
Xia, D ;
Yu, CA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (26) :24895-24902