Extracellular/Microenvironmental Redox State

被引:84
作者
Chaiswing, Luksana [2 ]
Oberley, Terry D. [1 ,2 ]
机构
[1] William S Middleton Mem Vet Adm Med Ctr, Pathol & Lab Med Serv, Madison, WI 53705 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Pathol & Lab Med, Madison, WI 53706 USA
关键词
EXTRACELLULAR-SUPEROXIDE-DISMUTASE; GAMMA-GLUTAMYL-TRANSPEPTIDASE; X(C)(-) CYSTINE/GLUTAMATE ANTIPORTER; PLASMA GLUTATHIONE-PEROXIDASE; PROTEIN DISULFIDE-ISOMERASE; NITRIC-OXIDE SYNTHASE; RENAL-CELL CARCINOMA; HYDROGEN-PEROXIDE; PROSTATE-CANCER; GROWTH-FACTOR;
D O I
10.1089/ars.2009.3020
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
Extracellular redox (reduction-oxidation) state is a factor that serves as an important regulator of cell-microenvironmental interactions and is determined by several known variables; including redox-modulating proteins that are located on the plasma membrane or outside of cells, extracellular thiol/disulfide couples, and reactive oxygen species (ROS)/reactive nitrogen species (RNS) that are capable of traveling across plasma membranes into the extracellular space. The extracellular redox state works in concert with the intracellular redox state to control both the influx and efflux of ROS/RNS that may serve to modulate redox signaling or to perturb normal cellular processes or both. Under physiologic conditions, the extracellular space is known to have a relatively more-oxidized redox state than the interior of the cell. During pathologic conditions, such as cancer, the extracellular redox state may be altered, causing specific proteins such as proteases, soluble factors, or the extracellular matrix to have altered functions or activities. Recent studies have strongly supported an important relation between the extracellular redox state and cancer cell aggressiveness. The purpose of this review is to identify redox buffer networks in extracellular spaces and to emphasize the possible roles of the extracellular redox state in cancer, knowledge that may contribute to potential therapeutic interventions. Antioxid. Redox Signal. 13, 449-465.
引用
收藏
页码:449 / 465
页数:17
相关论文
共 124 条
[1]   GAMMA-GLUTAMYL-TRANSFERASE TRANSPEPTIDASE (GAMMA-GT) AND MAINTENANCE OF THIOL POOLS IN TUMOR-CELLS RESISTANT TO ALKYLATING-AGENTS [J].
AHMAD, S ;
OKINE, L ;
WOOD, R ;
ALJIAN, J ;
VISTICA, DT .
JOURNAL OF CELLULAR PHYSIOLOGY, 1987, 131 (02) :240-246
[2]   Mechanisms of biological S-nitrosation and its measurement [J].
Akaike, T .
FREE RADICAL RESEARCH, 2000, 33 (05) :461-469
[3]   Antigen-presenting dendritic cells provide the reducing extracellular microenvironment required for T lymphocyte activation [J].
Angelini, G ;
Gardella, S ;
Ardy, M ;
Ciriolo, MR ;
Filomeni, G ;
Di Trapani, G ;
Clarke, F ;
Sitia, R ;
Rubartelli, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1491-1496
[4]   The thioredoxin system in cancer [J].
Arner, Elias S. J. ;
Holmgren, Arne .
SEMINARS IN CANCER BIOLOGY, 2006, 16 (06) :420-426
[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]   Heme, heme oxygenase, and ferritin: How the vascular endothelium survives (and dies) in an iron-rich environment [J].
Balla, Jozsef ;
Vercellotti, Gregory M. ;
Jeney, Viktoria ;
Yachie, Akihiro ;
Varga, Zsuzsa ;
Jacob, Harry S. ;
Eaton, John W. ;
Balla, Gyoergy .
ANTIOXIDANTS & REDOX SIGNALING, 2007, 9 (12) :2119-2137
[7]   Thioredoxin reductase as a pathophysiological factor and drug target [J].
Becker, K ;
Gromer, S ;
Schirmer, RH ;
Müller, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (20) :6118-6125
[8]   The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313
[9]   Evolution of antioxidant defence mechanisms [J].
Benzie, IFF .
EUROPEAN JOURNAL OF NUTRITION, 2000, 39 (02) :53-61
[10]   Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes [J].
Bienert, Gerd P. ;
Moller, Anders L. B. ;
Kristiansen, Kim A. ;
Schulz, Alexander ;
Moller, Ian M. ;
Schjoerring, Jan K. ;
Jahn, Thomas P. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (02) :1183-1192