PHLDA1, another PHLDA family protein that inhibits Akt

被引:43
作者
Chen, Yu [1 ,2 ]
Takikawa, Masahiro [1 ]
Tsutsumi, Shuichi [3 ]
Yamaguchi, Yoko [1 ,4 ]
Okabe, Atsushi [3 ,5 ]
Shimada, Mayuna [1 ,2 ]
Kawase, Tatsuya [1 ]
Sada, Akane [1 ]
Ezawa, Issei [1 ,2 ]
Takano, Yuhei [1 ]
Nagata, Kisaburo [4 ]
Suzuki, Yutaka [6 ]
Semba, Kentaro [2 ]
Aburatani, Hiroyuki [3 ]
Ohki, Rieko [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Lab Fundamental Oncol, Tokyo, Japan
[2] Waseda Univ, Grad Sch Adv Sci & Engn, Dept Life Sci & Med Biosci, Tokyo, Japan
[3] Univ Tokyo, Res Ctr Adv Sci & Technol, Genome Sci Div, Tokyo, Japan
[4] Toho Univ, Dept Biomol Sci, Fac Sci, Chiba, Japan
[5] Chiba Univ, Grad Sch Med, Dept Mol Oncol, Chiba, Japan
[6] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol & Med Sci, Lab Syst Genom, Chiba, Japan
来源
CANCER SCIENCE | 2018年 / 109卷 / 11期
关键词
Akt; p53; PH domain; PHLDA family; tumor suppressor; PLECKSTRIN HOMOLOGY DOMAINS; SQUAMOUS-CELL CARCINOMAS; PHOSPHOINOSITIDE BINDING; NEUROENDOCRINE TUMORS; DOWN-REGULATION; BREAST-CANCER; PH DOMAIN; EXPRESSION; GENE; CONTRIBUTES;
D O I
10.1111/cas.13796
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The PHLDA family (pleckstrin homology-like domain family) of genes consists of 3 members: PHLDA1, 2, and 3. Both PHLDA3 and PHLDA2 are phosphatidylinositol (PIP) binding proteins and function as repressors of Akt. They have tumor suppressive functions, mainly through Akt inhibition. Several reports suggest that PHLDA1 also has a tumor suppressive function; however, the precise molecular functions of PHLDA1 remain to be elucidated. Through a comprehensive screen for p53 target genes, we identified PHLDA1 as a novel p53 target, and we show that PHLDA1 has the ability to repress Akt in a manner similar to that of PHLDA3 and PHLDA2. PHLDA1 has a so-called split PH domain in which the PH domain is divided into an N-terminal (beta sheets 1-3) and a C-terminal (beta sheets 4-7 and an alpha-helix) portions. We show that the PH domain of PHLDA1 is responsible for its localization to the plasma membrane and binding to phosphatidylinositol. We also show that the function of the PH domain is essential for Akt repression. In addition, PHLDA1 expression analysis suggests that PHLDA1 has a tumor suppressive function in breast and ovarian cancers.
引用
收藏
页码:3532 / 3542
页数:11
相关论文
共 28 条
  • [1] IER5 generates a novel hypophosphorylated active form of HSF1 and contributes to tumorigenesis
    Asano, Yoshinori
    Kawase, Tatsuya
    Okabe, Atsushi
    Tsutsumi, Shuichi
    Ichikawa, Hitoshi
    Tatebe, Satoko
    Kitabayashi, Issay
    Tashiro, Fumio
    Namiki, Hideo
    Kondo, Tadashi
    Semba, Kentaro
    Aburatani, Hiroyuki
    Taya, Yoichi
    Nakagama, Hitoshi
    Ohki, Rieko
    [J]. SCIENTIFIC REPORTS, 2016, 6
  • [2] Distinct p53 Transcriptional Programs Dictate Acute DNA-Damage Responses and Tumor Suppression
    Brady, Colleen A.
    Jiang, Dadi
    Mello, Stephano S.
    Johnson, Thomas M.
    Jarvis, Lesley A.
    Kozak, Margaret M.
    Broz, Daniela Kenzelmann
    Basak, Shashwati
    Park, Eunice J.
    McLaughlin, Margaret E.
    Karnezis, Anthony N.
    Attardi, Laura D.
    [J]. CELL, 2011, 145 (04) : 571 - 583
  • [3] Expression of PAR-4 and PHLDA1 is prognostic for overall and disease-free survival in oral squamous cell carcinomas
    Coutinho-Camillo, Claudia Malheiros
    Lourenco, Silvia Vanessa
    Nonogaki, Suely
    Vartanian, Jose Guilherme
    Nagai, Maria Aparecida
    Kowalski, Luiz Paulo
    Soares, Fernando Augusto
    [J]. VIRCHOWS ARCHIV, 2013, 463 (01) : 31 - 39
  • [4] PHLDA1 Mediates Drug Resistance in Receptor Tyrosine Kinase-Driven Cancer
    Fearon, Abbie E.
    Carter, Edward P.
    Clayton, Natasha S.
    Wilkes, Edmund H.
    Baker, Ann-Marie
    Kapitonova, Ekaterina
    Bakhouche, Bakhouche A.
    Tanner, Yasmine
    Wang, Jun
    Gadaleta, Emanuela
    Chelala, Claude
    Moore, Kate M.
    Marshall, John F.
    Chupin, Juliette
    Schmid, Peter
    Jones, J. Louise
    Lockley, Michelle
    Cutillas, Pedro R.
    Grose, Richard P.
    [J]. CELL REPORTS, 2018, 22 (09): : 2469 - 2481
  • [5] Placental overgrowth in mice lacking the imprinted gene lpl
    Frank, D
    Fortino, W
    Clark, L
    Musalo, R
    Wang, WX
    Saxena, A
    Li, CM
    Reik, W
    Ludwig, T
    Tycko, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) : 7490 - 7495
  • [6] A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1:: tissue-specific expression, chromosomal location, and parental imprinting
    Frank, D
    Mendelsohn, CL
    Ciccone, E
    Svensson, K
    Ohlsson, R
    Tycko, B
    [J]. MAMMALIAN GENOME, 1999, 10 (12) : 1150 - 1159
  • [7] A proline- and glutamine-rich protein promotes apoptosis in neuronal cells
    Gomes, I
    Xiong, W
    Miki, T
    Rosner, MR
    [J]. JOURNAL OF NEUROCHEMISTRY, 1999, 73 (02) : 612 - 622
  • [8] TDAG51 is induced by homocysteine, promotes detachment-mediated programmed cell death, and contributes to the development of atherosclerosis in hyperhomocysteinemia
    Hossain, GS
    van Thienen, JV
    Werstuck, GH
    Zhou, J
    Sood, SK
    Dickhout, JG
    de Koning, ABL
    Tang, D
    Wu, DC
    Falk, E
    Poddar, R
    Jacobsen, DW
    Zhang, KZ
    Kaufman, RJ
    Austin, RC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) : 30317 - 30327
  • [9] PHLDA1 is a crucial negative regulator and effector of Aurora A kinase in breast cancer
    Johnson, Emmanuel O.
    Chang, Kuei-Hua
    de Pablo, Yolanda
    Ghosh, Soumitra
    Mehta, Rutika
    Badve, Sunil
    Shah, Kavita
    [J]. JOURNAL OF CELL SCIENCE, 2011, 124 (16) : 2711 - 2722
  • [10] An integrated map of p53-binding sites and histone modification in the human ENCODE regions
    Kaneshiro, Kiyofumi
    Tsutsumi, Shuichi
    Tsuji, Shingo
    Shirahige, Katsuhiko
    Aburatani, Hiroyuki
    [J]. GENOMICS, 2007, 89 (02) : 178 - 188