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Mol Cancer Res. 2005 Nov;3(11):627-34.

p53-independent regulation of p21Waf1/Cip1 expression and senescence by Chk2.

Author information

1
Oncology Discovery Research and Early Development, Johnson & Johnson Pharmaceutical Research and Early Development, Beerse, Belgium.

Abstract

The Chk2 kinase is a tumor suppressor and key component of the DNA damage checkpoint response that encompasses cell cycle arrest, apoptosis, and DNA repair. It has also been shown to have a role in replicative senescence resulting from dysfunctional telomeres. Some of these functions are at least partially exerted through activation of the p53 transcription factor. High-level expression of virally transduced Chk2 in A549 human lung carcinoma cells led to arrested proliferation, apoptosis, and senescence. These were accompanied by various molecular events, including p21(Waf1/Cip1) (p21) transcriptional induction, consistent with p53 activation. However, Chk2-dependent senescence and p21 transcriptional induction also occurred in p53-defective SK-BR-3 (breast carcinoma) and HaCaT (immortalized keratinocyte) cells. Small interfering RNA-mediated knockdown of p21 in p53-defective cells expressing Chk2 resulted in a decrease in senescent cells. These results revealed a p53-independent role for Chk2 in p21 induction and senescence that may contribute to tumor suppression and genotoxic treatment outcome.

PMID:
16317088
DOI:
10.1158/1541-7786.MCR-05-0121
[Indexed for MEDLINE]
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