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Title: ERK mediates anti-apoptotic effect through phosphorylation and cytoplasmic localization of p21 in response to DNA damage in normal human embryonic fibroblast (HEF) cells.
Authors: Jee-In Heo; Soo-Jin Oh; Yoon-Jung Kho; Jeong-Hyeon Kim; Hong-Joon Kang; Seong-Hoon Park; Hyun-Seok Kim; Jong-Yeon Shin; Min-Ju Kim; Sung Chan Kim; Jae-Bong Park; Jaebong Kim; Jae-Yong Lee
Abstract: Since anti-apoptotic effect of ERK has not been elucidated clearly in DNA-damage-induced cell death, the role of ERK was examined in normal HEF cells treated with mild DNA damage using etoposide or camptothecin. ERK was activated by DNA damage in HEF cells. PD98059 increased apoptosis and reduced DNA-damage-induced p21 level. Depletion of p21 induced cell death and PD98059 induced additional cell death. DNA-damage-induced increase in cytoplasmic localization and phosphorylation of threonine residues of p21 was reversed by PD98059. Thus, the results suggest that ERK pathway mediates anti-apoptotic effects through phosphorylation and cytoplasmic localization of p21 in response to mild DNA damage.
Subjects: CELL death; DNA damage; ETOPOSIDE; CAMPTOTHECIN; APOPTOSIS
Publication: Molecular Biology Reports, 2011, Vol 38, Issue 4, p2785
ISSN: 0301-4851
Publication type: Academic Journal
DOI: 10.1007/s11033-010-0423-5

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ERK mediates anti-apoptotic effect through phosphorylation and cytoplasmic localization of p21 in response to DNA damage in normal human embryonic fibroblast (HEF) cells.