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Study of PTEN subcellular localization

The tumor suppressor PTEN is a key regulator of a plethora of cellular processes that are crucial in cancer development. Through its lipid phosphatase activity PTEN suppresses the PI3K/AKT pathway to govern cell proliferation, growth, migration, energy metabolism and death. The repertoire of roles f...

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Detalles Bibliográficos
Autores principales: Bononi, Angela, Pinton, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396696/
https://www.ncbi.nlm.nih.gov/pubmed/25312582
http://dx.doi.org/10.1016/j.ymeth.2014.10.002
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author Bononi, Angela
Pinton, Paolo
author_facet Bononi, Angela
Pinton, Paolo
author_sort Bononi, Angela
collection PubMed
description The tumor suppressor PTEN is a key regulator of a plethora of cellular processes that are crucial in cancer development. Through its lipid phosphatase activity PTEN suppresses the PI3K/AKT pathway to govern cell proliferation, growth, migration, energy metabolism and death. The repertoire of roles fulfilled by PTEN has recently been expanded to include crucial functions in the nucleus, where it favors genomic stability and restrains cell cycle progression, as well as protein phosphatase dependent activity at the endoplasmic reticulum (ER) and mitochondria-associated membranes (MAMs), where PTEN interacts with the inositol 1,4,5-trisphosphate receptors (IP3Rs) and regulates Ca(2+) release from the ER and sensitivity to apoptosis. Indeed, PTEN is present in definite subcellular locations where it performs distinct functions acting on specific effectors. In this review, we summarize recent advantages in methods to study PTEN subcellular localization and the distinct biological functions of PTEN in different cellular compartments. A deeper understanding of PTEN’s compartmentalized-functions will guide the rational design of novel therapies.
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spelling pubmed-43966962015-05-01 Study of PTEN subcellular localization Bononi, Angela Pinton, Paolo Methods Article The tumor suppressor PTEN is a key regulator of a plethora of cellular processes that are crucial in cancer development. Through its lipid phosphatase activity PTEN suppresses the PI3K/AKT pathway to govern cell proliferation, growth, migration, energy metabolism and death. The repertoire of roles fulfilled by PTEN has recently been expanded to include crucial functions in the nucleus, where it favors genomic stability and restrains cell cycle progression, as well as protein phosphatase dependent activity at the endoplasmic reticulum (ER) and mitochondria-associated membranes (MAMs), where PTEN interacts with the inositol 1,4,5-trisphosphate receptors (IP3Rs) and regulates Ca(2+) release from the ER and sensitivity to apoptosis. Indeed, PTEN is present in definite subcellular locations where it performs distinct functions acting on specific effectors. In this review, we summarize recent advantages in methods to study PTEN subcellular localization and the distinct biological functions of PTEN in different cellular compartments. A deeper understanding of PTEN’s compartmentalized-functions will guide the rational design of novel therapies. Academic Press 2015-05-01 /pmc/articles/PMC4396696/ /pubmed/25312582 http://dx.doi.org/10.1016/j.ymeth.2014.10.002 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Bononi, Angela
Pinton, Paolo
Study of PTEN subcellular localization
title Study of PTEN subcellular localization
title_full Study of PTEN subcellular localization
title_fullStr Study of PTEN subcellular localization
title_full_unstemmed Study of PTEN subcellular localization
title_short Study of PTEN subcellular localization
title_sort study of pten subcellular localization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396696/
https://www.ncbi.nlm.nih.gov/pubmed/25312582
http://dx.doi.org/10.1016/j.ymeth.2014.10.002
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