Roles of Nox1 and other Nox isoforms in cancer development

被引:148
作者
Kamata, Tohru [1 ]
机构
[1] Shinshu Univ, Grad Sch Med, Dept Mol Biol & Biochem, Nagano, Japan
关键词
GENERATING NADPH OXIDASES; COLON EPITHELIAL-CELLS; NAD(P)H OXIDASE; DOWN-REGULATION; SUPEROXIDE; EXPRESSION; GROWTH; GENE; ACTIVATION; MUTATIONS;
D O I
10.1111/j.1349-7006.2009.01207.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The NADPH oxidase (Nox) family of enzymes generates reactive oxygen species (ROS). At low ROS concentration, intracellular signaling is initiated, whereas at high ROS concentration, oxidative stress is induced. The extensive studies over the years have shed light on the mediating roles of the Nox enzymes in a variety of normal physiological processes ranging from bactericidal activity to remodeling of the extracellular matrix. Consequently, imbalance of Nox activities could be the potential cause of acute or chronic diseases. With regard to functional relationships between Nox isoforms and pathogenesis, it is of particular interest to study whether they are involved in carcinogenesis, because overproduction of ROS has long been implicated as a risk factor in cancer development. We see one remarkable example of the causal relationship between Nox1 and cancer in Ras oncogene-induced cell transformation. Other studies also indicate that the Nox family of genes appears to be required for survival and growth of a subset of human cancer cells. Thus, the Nox family will be a focus of attention in cancer biology and etiology over the next couple years. (Cancer Sci 2009).
引用
收藏
页码:1382 / 1388
页数:7
相关论文
共 71 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]   Direct interaction of the novel nox proteins with p22phox is required for the formation of a functionally active NADPH oxidase [J].
Ambasta, RK ;
Kumar, P ;
Griendling, KK ;
Schmidt, HHHW ;
Busse, R ;
Brandes, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :45935-45941
[3]   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
[4]   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
[5]   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
[6]   A Ca2+-activated NADPH oxidase in testis, spleen, and lymph nodes [J].
Bánfi, B ;
Molnár, G ;
Maturana, A ;
Steger, K ;
Hegedûs, B ;
Demaurex, N ;
Krause, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (40) :37594-37601
[7]   The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313
[8]   An NAD(P)H oxidase regulates growth and transcription in melanoma cells [J].
Brar, SS ;
Kennedy, TP ;
Sturrock, AB ;
Huecksteadt, TP ;
Quinn, MT ;
Whorton, AR ;
Hoidal, JR .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 282 (06) :C1212-C1224
[9]   Transcriptional regulation of the NADPH oxidase isoform, Nox1, in colon epithelial cells: Role of GATA-binding factor(s) [J].
Brewer, AC ;
Sparks, EC ;
Shah, AM .
FREE RADICAL BIOLOGY AND MEDICINE, 2006, 40 (02) :260-274
[10]   p190 RhoGAP is the principal Src substrate in brain and regulates axon outgrowth, guidance and fasciculation [J].
Brouns, MR ;
Matheson, SF ;
Settleman, J .
NATURE CELL BIOLOGY, 2001, 3 (04) :361-367