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Regulation of PP2A by Sphingolipid Metabolism and Signaling

Protein phosphatase 2A (PP2A) is a serine/threonine phosphatase that is a primary regulator of cellular proliferation through targeting of proliferative kinases, cell cycle regulators, and apoptosis inhibitors. It is through the regulation of these regulatory elements that gives PP2A tumor suppresso...

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Detalles Bibliográficos
Autores principales: Oaks, Joshua, Ogretmen, Besim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295541/
https://www.ncbi.nlm.nih.gov/pubmed/25642418
http://dx.doi.org/10.3389/fonc.2014.00388
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author Oaks, Joshua
Ogretmen, Besim
author_facet Oaks, Joshua
Ogretmen, Besim
author_sort Oaks, Joshua
collection PubMed
description Protein phosphatase 2A (PP2A) is a serine/threonine phosphatase that is a primary regulator of cellular proliferation through targeting of proliferative kinases, cell cycle regulators, and apoptosis inhibitors. It is through the regulation of these regulatory elements that gives PP2A tumor suppressor functions. In addition to mutations on the regulatory subunits, the phosphatase/tumor suppressing activity of PP2A is also inhibited in several cancer types due to overexpression or modification of the endogenous PP2A inhibitors such as SET/I2PP2A. This review focuses on the current literature regarding the interactions between the lipid signaling molecules, selectively sphingolipids, and the PP2A inhibitor SET for the regulation of PP2A, and the therapeutic potential of sphingolipids as PP2A activators for tumor suppression via targeting SET oncoprotein.
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spelling pubmed-42955412015-01-30 Regulation of PP2A by Sphingolipid Metabolism and Signaling Oaks, Joshua Ogretmen, Besim Front Oncol Oncology Protein phosphatase 2A (PP2A) is a serine/threonine phosphatase that is a primary regulator of cellular proliferation through targeting of proliferative kinases, cell cycle regulators, and apoptosis inhibitors. It is through the regulation of these regulatory elements that gives PP2A tumor suppressor functions. In addition to mutations on the regulatory subunits, the phosphatase/tumor suppressing activity of PP2A is also inhibited in several cancer types due to overexpression or modification of the endogenous PP2A inhibitors such as SET/I2PP2A. This review focuses on the current literature regarding the interactions between the lipid signaling molecules, selectively sphingolipids, and the PP2A inhibitor SET for the regulation of PP2A, and the therapeutic potential of sphingolipids as PP2A activators for tumor suppression via targeting SET oncoprotein. Frontiers Media S.A. 2015-01-15 /pmc/articles/PMC4295541/ /pubmed/25642418 http://dx.doi.org/10.3389/fonc.2014.00388 Text en Copyright © 2015 Oaks and Ogretmen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Oaks, Joshua
Ogretmen, Besim
Regulation of PP2A by Sphingolipid Metabolism and Signaling
title Regulation of PP2A by Sphingolipid Metabolism and Signaling
title_full Regulation of PP2A by Sphingolipid Metabolism and Signaling
title_fullStr Regulation of PP2A by Sphingolipid Metabolism and Signaling
title_full_unstemmed Regulation of PP2A by Sphingolipid Metabolism and Signaling
title_short Regulation of PP2A by Sphingolipid Metabolism and Signaling
title_sort regulation of pp2a by sphingolipid metabolism and signaling
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295541/
https://www.ncbi.nlm.nih.gov/pubmed/25642418
http://dx.doi.org/10.3389/fonc.2014.00388
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