%0 Journal Article
%T DNA-dependent protein kinase catalytic subunit modulates the stability of c-Myc oncoprotein
%A Jing An
%A Dong-Yan Yang
%A Qin-Zhi Xu
%A Shi-Meng Zhang
%A Yan-Ying Huo
%A Zeng-Fu Shang
%A Yu Wang
%A De-Chang Wu
%A Ping-Kun Zhou
%J Molecular Cancer
%D 2008
%I BioMed Central
%R 10.1186/1476-4598-7-32
%X Firstly, siRNA-mediated silencing of DNA-PKcs strikingly downregulated c-Myc protein levels in HeLa and HepG2 cells, and simultaneously decreased cell proliferation. The c-Myc protein level in DNA-PKcs deficient human glioma M059J cells was also found much lower than that in DNA-PKcs efficient M059K cells. ATM deficiency does not affect c-Myc expression level. Silencing of DNA-PKcs in HeLa cells resulted in a decreased stability of c-Myc protein, which was associated the increasing of c-Myc phosphorylation on Thr58/Ser62 and ubiquitination level. Phosphorylation of Akt on Ser473, a substrate of DNA-PKcs was found decreased in DNA-PKcs deficient cells. As the consequence, the phosphorylation of GSK3 ¦Â on Ser9, a negatively regulated target of Akt, was also decreased, and which led to activation of GSK 3¦Â and in turn phosphorylation of c-Myc on Thr58. Moreover, inhibition of GSK3 activity by LiCl or specific siRNA molecules rescued the downregulation of c-Myc mediated by silencing DNA-PKcs. Consistent with this depressed DNA-PKcs cell model, overexpressing DNA-PKcs in normal human liver L02 cells, by sub-chronically exposing to very low dose of carcinogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), increased c-Myc protein level, the phosphorylation of Akt and GSK3 ¦Â, as well as cell proliferation. siRNA-mediated silencing of DNA-PKcs in this cell model reversed above alterations to the original levels of L02 cells.A suitable DNA-PKcs level in cells is necessary for maintaining genomic stability, while abnormal overexpression of DNA-PKcs may contribute to cell proliferation and even oncogenic transformation by stabilizing the c-Myc oncoprotein via at least the Akt/GSK3 pathway. Our results suggest DNA-PKcs a novel biological role beyond its DNA repair function.The c-Myc oncoprotein is a short-lived basic helix-loop-helix leucine-zipper transcription factor that, together with its dimerization partner Max, binds to specific E-box sequences and is responsible for control
%U http://www.molecular-cancer.com/content/7/1/32