KMID : 0578320090280050489
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Molecules and Cells 2009 Volume.28 No. 5 p.489 ~ p.494
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The p53-p21Cip1/WAF1 pathway is necessary for cellular senescence induced by the inhibition of protein kinase CKII in human colon cancer cells
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Kang Ji-Young
Kim Jin-Joo Jang Seok-Young Bae Young-Seuk
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Abstract
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We have previously shown that the down-regulation of protein kinase CKII activity is tightly associated with cellular senescence of human fibroblast IMR-90 cells. Here, we examined the roles of p53 and p21Cip1/WAF1 in senescence development induced by CKII inhibition using wild-type, isogenic p53-/- and isogenic p21-/- HCT116 human colon cancer cell lines. A senescent marker appeared after staining for senescence-associated ¥â-galactosidase activity in wild-type HCT116 cells treated with CKII inhibitor or CKII¥á siRNA, but this response was almost abolished in p53- or p21Cip1/WAF1-null cells. Increased cellular levels of p53 and p21Cip1/WAF1 protein occurred with the inhibition of CKII. CKII inhibition upregulated p53 and p21Cip1/WAF1 expression at post-transcriptional level and transcription level, respectively. RB phosphorylation significantly decreased in cells treated with CKII inhibitor. Taken together, this study shows that the activation of the p53?p21Cip1/WAF1 pathway acts as a major mediator of cellular senescence induced by CKII inhibition.
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KEYWORD
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human colon cancer cell, p21Cip1/WAF1, p53, protein kinase CKII, senescence
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