PH Domain-Only Protein PHLDA3 Is a p53-Regulated Repressor of Akt

被引:195
作者
Kawase, Tatsuya [1 ,8 ,9 ]
Ohki, Rieko [1 ,9 ]
Shibata, Tatsuhiro [2 ,3 ]
Tsutsumi, Shuichi [7 ]
Kamimura, Naoko [7 ]
Inazawa, Johji [6 ]
Ohta, Tsutomu [4 ]
Ichikawa, Hitoshi [5 ]
Aburatani, Hiroyuki [7 ]
Tashiro, Fumio [8 ]
Taya, Yoichi [1 ,9 ,10 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Radiobiol, Chuo Ku, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Res Inst, Canc Genom Project, Chuo Ku, Tokyo 1040045, Japan
[3] Natl Canc Ctr, Res Inst, Div Pathol, Chuo Ku, Tokyo 1040045, Japan
[4] Natl Canc Ctr, Res Inst, Ctr Med Genom, Chuo Ku, Tokyo 1040045, Japan
[5] Natl Canc Ctr, Res Inst, Canc Transcriptome Project, Chuo Ku, Tokyo 1040045, Japan
[6] Tokyo Med & Dent Univ, Med Res Inst, Dept Mol Cytogenet, Bunkyo Ku, Tokyo 1138510, Japan
[7] Univ Tokyo, Adv Sci & Technol Res Ctr, Genome Sci Div, Meguro Ku, Tokyo 1538904, Japan
[8] Tokyo Univ Sci, Fac Ind Sci & Technol, Dept Biol Sci & Technol, Noda, Chiba 2708510, Japan
[9] SORST JST, Kawaguchi, Saitama 3320012, Japan
[10] Natl Univ Singapore, Ctr Life Sci, Canc Res Ctr Excellence, Singapore 117456, Singapore
基金
日本学术振兴会;
关键词
GENOMIC HYBRIDIZATION ANALYSIS; PLECKSTRIN-HOMOLOGY DOMAINS; CANDIDATE MEDIATOR; KINASE B; P53; ACTIVATION; PATHWAY; LUNG; FAMILY; CANCER;
D O I
10.1016/j.cell.2008.12.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p53 and Akt are critical players regulating tumorigenesis with opposite effects: whereas p53 transactivates target genes to exert its function as a tumor suppressor, Akt phosphorylates its substrates and transduces downstream survival signals. In addition, p53 and Akt negatively regulate each other to balance survival and death signals within a cell. We now identify PHLDA3 as a p53 target gene that encodes a PH domain-only protein. We find that PHLDA3 competes with the PH domain of Akt for binding of membrane lipids, thereby inhibiting Akt translocation to the cellular membrane and activation. Ablation of endogenous PHLDA3 results in enhanced Akt activity and decrease of p53-dependent apoptosis. We also demonstrate the suppression of anchorage-independent cell growth by PHLDA3. Loss of the PHLDA3 genomic locus was frequently observed in primary lung cancers, suggesting a role of PHLDA3 in tumor suppression. Our results reveal a new mode of coordination between the p53 and Akt pathways.
引用
收藏
页码:535 / 550
页数:16
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