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PHLDA1, another PHLDA family protein that inhibits Akt
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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215895/ https://www.ncbi.nlm.nih.gov/pubmed/30207029 http://dx.doi.org/10.1111/cas.13796 |
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author | Chen, Yu Takikawa, Masahiro Tsutsumi, Shuichi Yamaguchi, Yoko Okabe, Atsushi Shimada, Mayuna Kawase, Tatsuya Sada, Akane Ezawa, Issei Takano, Yuhei Nagata, Kisaburo Suzuki, Yutaka Semba, Kentaro Aburatani, Hiroyuki Ohki, Rieko |
author_facet | Chen, Yu Takikawa, Masahiro Tsutsumi, Shuichi Yamaguchi, Yoko Okabe, Atsushi Shimada, Mayuna Kawase, Tatsuya Sada, Akane Ezawa, Issei Takano, Yuhei Nagata, Kisaburo Suzuki, Yutaka Semba, Kentaro Aburatani, Hiroyuki Ohki, Rieko |
author_sort | Chen, Yu |
collection | PubMed |
description | 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 (β sheets 1‐3) and a C‐terminal (β sheets 4‐7 and an α‐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. |
format | Online Article Text |
id | pubmed-6215895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62158952018-11-08 PHLDA1, another PHLDA family protein that inhibits Akt Chen, Yu Takikawa, Masahiro Tsutsumi, Shuichi Yamaguchi, Yoko Okabe, Atsushi Shimada, Mayuna Kawase, Tatsuya Sada, Akane Ezawa, Issei Takano, Yuhei Nagata, Kisaburo Suzuki, Yutaka Semba, Kentaro Aburatani, Hiroyuki Ohki, Rieko Cancer Sci Original Articles 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 (β sheets 1‐3) and a C‐terminal (β sheets 4‐7 and an α‐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. John Wiley and Sons Inc. 2018-10-13 2018-11 /pmc/articles/PMC6215895/ /pubmed/30207029 http://dx.doi.org/10.1111/cas.13796 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Chen, Yu Takikawa, Masahiro Tsutsumi, Shuichi Yamaguchi, Yoko Okabe, Atsushi Shimada, Mayuna Kawase, Tatsuya Sada, Akane Ezawa, Issei Takano, Yuhei Nagata, Kisaburo Suzuki, Yutaka Semba, Kentaro Aburatani, Hiroyuki Ohki, Rieko PHLDA1, another PHLDA family protein that inhibits Akt |
title |
PHLDA1, another PHLDA family protein that inhibits Akt |
title_full |
PHLDA1, another PHLDA family protein that inhibits Akt |
title_fullStr |
PHLDA1, another PHLDA family protein that inhibits Akt |
title_full_unstemmed |
PHLDA1, another PHLDA family protein that inhibits Akt |
title_short |
PHLDA1, another PHLDA family protein that inhibits Akt |
title_sort | phlda1, another phlda family protein that inhibits akt |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215895/ https://www.ncbi.nlm.nih.gov/pubmed/30207029 http://dx.doi.org/10.1111/cas.13796 |
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