Aiding and abetting roles of NOX oxidases in cellular transformation

被引:240
作者
Block, Karen [1 ,2 ]
Gorin, Yves [2 ]
机构
[1] S Texas Vet Hlth Care Syst, Audie L Murphy Mem Hosp Div, Dept Med MC 7882, San Antonio, TX 78229 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Med MC 7882, San Antonio, TX 78229 USA
关键词
GENERATING NADPH OXIDASE; ADENINE-DINUCLEOTIDE PHOSPHATE; ACTIVATE SUPEROXIDE GENERATION; OXYGEN SPECIES GENERATION; TUMOR-SUPPRESSOR PROTEIN; BREAST-CANCER CELLS; REACTIVE OXYGEN; NAD(P)H OXIDASE; GROWTH-FACTOR; OXIDATIVE STRESS;
D O I
10.1038/nrc3339
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
NADPH oxidases of the NADPH oxidase (NOX) family are dedicated reactive oxygen species-generating enzymes that broadly and specifically regulate redox-sensitive signalling pathways that are involved in cancer development and progression. They act at specific cellular membranes and microdomains through the activation of oncogenes and the inactivation of tumour suppressor proteins. In this Review, we discuss primary targets and redox-linked signalling systems that are influenced by NOX-derived ROS, and the biological role of NOX oxidases in the aetiology of cancer.
引用
收藏
页码:627 / 637
页数:11
相关论文
共 190 条
[1]   Oncogenic Ras upregulates NADPH oxidase 1 gene expression through MEK-ERK-dependent phosphorylation of GATA-6 [J].
Adachi, Y. ;
Shibai, Y. ;
Mitsushita, J. ;
Shang, W. H. ;
Hirose, K. ;
Kamata, T. .
ONCOGENE, 2008, 27 (36) :4921-4932
[2]   Upregulation of Nox4 by Hypertrophic Stimuli Promotes Apoptosis and Mitochondrial Dysfunction in Cardiac Myocytes [J].
Ago, Tetsuro ;
Kuroda, Junya ;
Pain, Jayashree ;
Fu, Cexiong ;
Li, Hong ;
Sadoshima, Junichi .
CIRCULATION RESEARCH, 2010, 106 (07) :1253-U183
[3]  
Almo Steven C., 2007, Journal of Structural and Functional Genomics, V8, P121, DOI 10.1007/s10969-007-9036-1
[4]   Reactive oxygen generated by Nox1 triggers the angiogenic switch [J].
Arbiser, JL ;
Petros, J ;
Klafter, R ;
Govindajaran, B ;
McLaughlin, ER ;
Brown, LF ;
Cohen, C ;
Moses, M ;
Kilroy, S ;
Arnold, RS ;
Lambeth, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :715-720
[5]   Nox1 expression determines cellular reactive oxygen and modulates c-fos-induced growth factor, interleukin-8, and Cav-1 [J].
Arnold, Rebecca S. ;
He, Ju ;
Remo, Andrea ;
Ritsick, Darren ;
Yin-Goen, Qiqin ;
Lambeth, J. David ;
Datta, Milton W. ;
Young, Andrew N. ;
Petros, John A. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 171 (06) :2021-2032
[6]   Epidermal growth factor (EGF)-induced generation of hydrogen peroxide - Role in EGF receptor-mediated tyrosine phosphorylation [J].
Bae, YS ;
Kang, SW ;
Seo, MS ;
Baines, IC ;
Tekle, E ;
Chock, PB ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (01) :217-221
[7]   Phosphatidylinositol 3-kinase-dependent membrane recruitment of Rac-1 and p47phox is critical for α-platelet-derived growth factor receptor-induced production of reactive oxygen species [J].
Baeumer, Anselm T. ;
ten Freyhaus, Henrik ;
Sauer, Heinrich ;
Wartenberg, Maria ;
Kappert, Kai ;
Schnabel, Petra ;
Konkol, Christian ;
Hescheler, Juergen ;
Vantler, Marius ;
Rosenkranz, Stephan .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (12) :7864-7876
[8]   NOX3, a superoxide-generating NADPH oxidase of the inner ear [J].
Bánfi, B ;
Malgrange, B ;
Knisz, J ;
Steger, K ;
Dubois-Dauphin, M ;
Krause, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :46065-46072
[9]   Two novel proteins activate superoxide generation by the NADPH oxidase NOX1 [J].
Bánfi, B ;
Clark, RA ;
Steger, K ;
Krause, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :3510-3513
[10]   A mammalian H+ channel generated through alternative splicing of the NADPH oxidase homolog NOH-1 [J].
Bánfi, B ;
Maturana, A ;
Jaconi, S ;
Arnaudeau, S ;
Laforge, T ;
Sinha, B ;
Ligeti, E ;
Demaurex, N ;
Krause, KH .
SCIENCE, 2000, 287 (5450) :138-142