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NADPH oxidase is involved in protein kinase CKII down-regulation-mediated senescence through elevation of the level of reactive oxygen species in human colon cancer cells
被引:25
|作者:
Jeon, Seon Min
[1
]
Lee, Sung-Jin
[2
]
Kwon, Taeg Kyu
[3
]
Kim, Kyung-Jin
[4
]
Bae, Young-Seuk
[1
]
机构:
[1] Kyungpook Natl Univ, Sch Life Sci & Biotechnol, Coll Nat Sci, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Taegu 700422, South Korea
[3] Keimyung Univ, Sch Med, Dept Immunol, Taegu 700712, South Korea
[4] Pohang Univ Sci & Technol, Pohang Accelerator Lab, Pohang 790784, Kyungbuk, South Korea
关键词:
Senescence;
Protein kinase CKII;
Superoxide anion;
NADPH oxidase;
p53;
activation;
HUMAN FIBROBLASTS;
SUPEROXIDE-PRODUCTION;
CELLULAR SENESCENCE;
INHIBITORS;
P16(INK4A);
P53;
D O I:
10.1016/j.febslet.2010.05.054
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:
We have shown that protein kinase CKII (CKII) inhibition induces senescence through the p53-dependent pathway in HCT116 cells. Here we examined the molecular mechanism through which CKII inhibition activates p53 in HCT116 cells. CKII inhibition by treatment with CKII inhibitor or CKII alpha small-interfering RNA (siRNA) increased intracellular hydrogen peroxide and superoxide anion levels. These effects were significantly blocked by pretreatment of cells with the antioxidant N-acetylcysteine. Additionally, NADPH oxidase (NOX) inhibitor apocynin and p22(phox) siRNA significantly reduced p53 expression and suppressed the appearance of senescence markers. CKII inhibition did not affect mitochondrial superoxide generation. These data demonstrate that CKII inhibition induces superoxide anion generation via NOX activation, and subsequent superoxide-dependent activation of p53 acts as a mediator of senescence in HCT116 cells after down-regulation of CKII. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:3137 / 3142
页数:6
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