Vitamin C inhibits p53-induced replicative senescence through suppression of ROS production and p38 MAPK activity |
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Authors: | Kim Jee-Eun Jin Dong-Hoon Lee Soon-Duck Hong Seung-Woo Shin Jae-Sik Lee Seung-Koo Jung Da-Jung Kang Jae-Seung Lee Wang-Jae |
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Affiliation: | Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine, Jongno-Gu, Seoul, Korea. |
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Abstract: | We previously reported that tumor cells expressing p53 increase intracellular levels of reactive oxygen species (ROS). In this study, we described an inhibitory effect of vitamin C on replicative senescence. Vitamin C was found to inhibit p53-induced senescence in human bladder cancer EJ cells. The senescence-like phenotype (SLP) induced by p53, which showed a morphological change and an irreversible cell cycle arrest, was not observed in vitamin C-treated EJ cells. In addition, vitamin C did not significantly affect normal cell proliferation. We investigated the molecular mechanisms of the inhibitory effect of vitamin C on the development of replicative senescence in EJ cells. We found that vitamin C inhibited this p53-induced ROS generation. Moreover, p38 kinase which was activated during p53-induced senescence was not observed in vitamin C-treated EJ cells. SB203580, a chemical inhibitor of p38 kinase, was found to consistently inhibit p53-induced senescence. Therefore, it is suggested that vitamin C inhibits p53-induced senescence by preventing ROS generation, which in turn leads to the activation of p38 MAPKinase. These results reveal the inhibitory mechanism of vitamin C on cellular senescence. |
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