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PHLDA1, another PHLDA family protein that inhibits Akt.
- Source :
-
Cancer science [Cancer Sci] 2018 Nov; Vol. 109 (11), pp. 3532-3542. Date of Electronic Publication: 2018 Oct 13. - Publication Year :
- 2018
-
Abstract
- 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.<br /> (© 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.)
- Subjects :
- Alternative Splicing
Animals
Cell Line, Tumor
Cell Membrane metabolism
Female
Gene Expression Regulation, Neoplastic
HCT116 Cells
HEK293 Cells
HeLa Cells
Humans
Neoplasm Transplantation
Phosphatidylinositols metabolism
Protein Binding
Transcription Factors chemistry
Breast Neoplasms genetics
Ovarian Neoplasms genetics
Proto-Oncogene Proteins c-akt metabolism
Transcription Factors genetics
Transcription Factors metabolism
Tumor Suppressor Protein p53 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1349-7006
- Volume :
- 109
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Cancer science
- Publication Type :
- Academic Journal
- Accession number :
- 30207029
- Full Text :
- https://doi.org/10.1111/cas.13796