Expanding roles of superoxide dismutases in cell regulation and cancer

被引:248
作者
Che, Meixia [1 ,2 ]
Wang, Ren [3 ]
Li, Xiaoxing [3 ]
Wang, Hui-Yun [1 ,2 ,3 ]
Zheng, X. F. Steven [1 ,2 ,3 ]
机构
[1] Rutgers State Univ, Robert Wood Johnson Med Sch, Rutgers Canc Inst New Jersey, New Brunswick, NJ 08903 USA
[2] Rutgers State Univ, Robert Wood Johnson Med Sch, Dept Pharmacol, New Brunswick, NJ 08903 USA
[3] Sun Yat Sen Univ, Ctr Canc, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
关键词
HYDROGEN-PEROXIDE; OXIDATIVE STRESS; LUNG ADENOCARCINOMA; DNA-DAMAGE; REVERSIBLE INACTIVATION; ECSOD EXPRESSION; COPPER-BINDING; OXYGEN; SOD1; MITOCHONDRIAL;
D O I
10.1016/j.drudis.2015.10.001
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Reactive oxygen species (ROS) have important roles in normal physiology and diseases, particularly cancer. Under normal physiological conditions, they participate in redox reactions and serve as second messengers for regulatory functions. Owing to aberrant metabolism, cancer cells accumulate excessive ROS, thus requiring a robustly active antioxidant system to prevent cellular damage. Superoxide dismutases (SODs) are enzymes that catalyze the removal of superoxide free radicals. There are three distinct members of this metalloenzyme family in mammals: SOD1 (Cu/ZnSOD), SOD2 (MnSOD) and SOD3 (ecSOD). SODs are increasingly recognized for their regulatory functions in growth, metabolism and oxidative stress responses, which are also crucial for cancer development and survival. Growing evidence shows that SODs are also potentially useful anticancer drug targets. This review will focus on recent research of SODs in cellular regulation, with emphasis on their roles in cancer biology and therapy.
引用
收藏
页码:143 / 149
页数:7
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