Published online before print May 10, 2007

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Copyright © 2007 American Society for Investigative Pathology
American Journal of Pathology, doi:10.2353/ajpath.2007.070121

Accepted for publication April 3, 2007.

Article

The Induction of Growth Arrest DNA Damage-Inducible Gene 45 in Human Hepatoma Cell Lines by S-Adenosylmethionine

Weihua Qiu^*, Bingsen Zhou^*, Peiguo G. Chu, Frank Luh^*, and Yun Yen^*@

From the Departments of Clinical and Molecular Pharmacology* and Pathology, City of Hope National Medical Center, Duarte, California; and the Department of Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

^@ To whom correspondence should be addressed. E-mail: yyen{at}coh.org.

	Abstract

Down-regulation of GADD45, which is known to influence cell growth control, apoptosis, and cellular response to DNA damage, has been verified to be specific in hepatocellular carcinoma and consistent with the degree of malignancy. Here, we identified promoter elements for several transcriptional factors in the proximal promoter of GADD45 using the luciferase assay. As a methyl donor for biological transmethylation reactions, S-adenosylmethionine (SAMe) could restore GADD45 expression in HepG2 in Northern blot analyses and quantitative real-time polymerase chain reaction. Activity and binding capacity of nuclear factor (NF)-B were confirmed to be specifically induced by SAMe, as evidenced by electrophoretic mobility shift assay, enzyme-linked immunosorbent assay, and a decrease of IB in Western blot analyses. The most upstream NF-B-binding site was crucial for transcriptional activation. In contrast to NF-B, although there is an E2F-1-binding site adjacent to the NF-B sites, treatment with SAMe could not induce E2F-1-binding activity. Despite showing a similar GADD45 promoter regulatory pattern as HepG2 (p53 wild type), Hep3B (p53-null) did not exhibit GADD45 induction by SAMe, and the induction could be partially recovered on reconstituting p53 in Hep3B. Thus, our results suggest that GADD45 induction by SAMe via NF-B may represent a novel mechanism of SAMe-mediated hepatoprotection, with p53 playing an important role.