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:26
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.
引用
收藏
页码:3137 / 3142
页数:6
相关论文
共 46 条
  • [41] Role of reactive oxygen species in brucein D-mediated p38-mitogen-activated protein kinase and nuclear factor-κB signalling pathways in human pancreatic adenocarcinoma cells
    Lau, S. T.
    Lin, Z. X.
    Leung, P. S.
    [J]. BRITISH JOURNAL OF CANCER, 2010, 102 (03) : 583 - 593
  • [42] Role of NOX1 and NOX5 in protein kinase C/reactive oxygen species-mediated MMP-9 activation and invasion in MCF-7 breast cancer cells
    Song, Hyun-Kyung
    Kim, Jeong-Mi
    Noh, Eun-Mi
    Youn, Hyun Jo
    Lee, Young-Rae
    [J]. MOLECULAR MEDICINE REPORTS, 2024, 30 (04)
  • [43] p34SEI-1 Inhibits Doxorubicin-Induced Senescence through a Pathway Mediated by Protein Kinase C-δ and c-Jun-NH2-Kinase 1 Activation in Human Breast Cancer MCF7 Cells
    Lee, Sae Lo Oom
    Hong, Seung-Woo
    Shin, Jae-Sik
    Kim, Jin Sun
    Ko, Seong-Gyu
    Hong, Nam-Joo
    Kim, Dae Jin
    Lee, Wang-Jae
    Jin, Dong-Hoon
    Lee, Myeong-Sok
    [J]. MOLECULAR CANCER RESEARCH, 2009, 7 (11) : 1845 - 1853
  • [44] 6-Dehydrogingerdione, an active constituent of dietary ginger, induces cell cycle arrest and apoptosis through reactive oxygen species/c-Jun N-terminal kinase pathways in human breast cancer cells
    Hsu, Ya-Ling
    Chen, Chung-Yi
    Hou, Ming-Feng
    Tsai, Eing-Mei
    Jong, Yuh-Jyh
    Hung, Chih-Hsing
    Kuo, Po-Lin
    [J]. MOLECULAR NUTRITION & FOOD RESEARCH, 2010, 54 (09) : 1307 - 1317
  • [45] Down-regulation of cyclin-dependent kinase-4 and MAPK through estrogen receptor mediated cell cycle arrest in human breast cancer induced by gold nanoparticle tagged toxin protein NKCT1
    Bhowmik, Tanmoy
    Gomes, Antony
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 2017, 268 : 119 - 128
  • [46] (1S,2S,3E,7E,11E)-3,7,11,15-Cembratetraen-17,2-olide, a Cembrenolide Diterpene from Soft Coral Lobophytum sp., Inhibits Growth and Induces Apoptosis in Human Colon Cancer Cells through Reactive Oxygen Species Generation
    Hong, Ji-Young
    Boo, Hye-Jin
    Kang, Jung-Il
    Kim, Min-Kyoung
    Yoo, Eun-Sook
    Hyun, Jin-Won
    Koh, Young-Sang
    Kim, Gi Young
    Maeng, Young Hee
    Hyun, Chang Lim
    Chang, Weon Young
    Kim, Young Ho
    Kim, Young Ree
    Kang, Hee-Kyoung
    [J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2012, 35 (07) : 1054 - 1063