| Literature DB >> 24003224 |
Hiroaki Iwasa1, Takumi Kudo, Sainawaer Maimaiti, Mitsunobu Ikeda, Junichi Maruyama, Kentaro Nakagawa, Yutaka Hata.
Abstract
Ras association domain family (RASSF) 6 is a member of the C-terminal RASSF proteins such as RASSF1A and RASSF3. RASSF6 is involved in apoptosis in various cells under miscellaneous conditions, but it remains to be clarified how RASSF6 exerts tumor-suppressive roles. We reported previously that RASSF3 facilitates the degradation of MDM2, a major E3 ligase of p53, and stabilizes p53 to function as a tumor suppressor. In this study, we demonstrate that RASSF6 overexpression induces G1/S arrest in p53-positive cells. Its depletion prevents UV- and VP-16-induced apoptosis and G1/S arrest in HCT116 and U2OS cells. RASSF6-induced apoptosis partially depends on p53. RASSF6 binds MDM2 and facilitates its ubiquitination. RASSF6 depletion blocks the increase of p53 in response to UV exposure and up-regulation of p53 target genes. RASSF6 depletion delays DNA repair in UV- and VP-16-treated cells and increases polyploid cells after VP-16 treatment. These findings indicate that RASSF6 stabilizes p53, regulates apoptosis and the cell cycle, and functions as a tumor suppressor. Together with the previous reports regarding RASSF1A and RASSF3, the stabilization of p53 may be the common function of the C-terminal RASSF proteins.Entities:
Keywords: Apoptosis; Checkpoint Control; DNA Damage; Hippo Pathway; RASSF; Tumor Suppressor Gene; p53
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Year: 2013 PMID: 24003224 PMCID: PMC3798497 DOI: 10.1074/jbc.M113.507384
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157