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GRP78 at the Centre of the Stage in Cancer and Neuroprotection
The 78-kDa glucose-regulated protein GRP78, also known as BiP and HSP5a, is a multifunctional protein with activities far beyond its well-known role in the unfolded protein response (UPR) which is activated after endoplasmic reticulum (ER) stress in the cells. Most of these newly discovered activiti...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380735/ https://www.ncbi.nlm.nih.gov/pubmed/28424579 http://dx.doi.org/10.3389/fnins.2017.00177 |
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author | Casas, Caty |
author_facet | Casas, Caty |
author_sort | Casas, Caty |
collection | PubMed |
description | The 78-kDa glucose-regulated protein GRP78, also known as BiP and HSP5a, is a multifunctional protein with activities far beyond its well-known role in the unfolded protein response (UPR) which is activated after endoplasmic reticulum (ER) stress in the cells. Most of these newly discovered activities depend on its position within the cell. GRP78 is located mainly in the ER, but it has also been observed in the cytoplasm, the mitochondria, the nucleus, the plasma membrane, and secreted, although it is dedicated mostly to engage endogenous cytoprotective processes. Hence, GRP78 may control either UPR and macroautophagy or may activated phosphatidylinositol 3-kinase (PI3K)/AKT pro-survival pathways. GRP78 influences how tumor cells survive, proliferate, and develop chemoresistance. In neurodegeneration, endogenous mechanisms of neuroprotection are frequently insufficient or dysregulated. Lessons from tumor biology may give us clues about how boosting endogenous neuroprotective mechanisms in age-related neurodegeneration. Herein, the functions of GRP78 are revealed at the center of the stage of apparently opposite sites of the same coin regarding cytoprotection: neurodegeneration and cancer. The goal is to give a comprehensive and critical review that may serve to guide future experiments to identify interventions that will enhance neuroprotection. |
format | Online Article Text |
id | pubmed-5380735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53807352017-04-19 GRP78 at the Centre of the Stage in Cancer and Neuroprotection Casas, Caty Front Neurosci Neuroscience The 78-kDa glucose-regulated protein GRP78, also known as BiP and HSP5a, is a multifunctional protein with activities far beyond its well-known role in the unfolded protein response (UPR) which is activated after endoplasmic reticulum (ER) stress in the cells. Most of these newly discovered activities depend on its position within the cell. GRP78 is located mainly in the ER, but it has also been observed in the cytoplasm, the mitochondria, the nucleus, the plasma membrane, and secreted, although it is dedicated mostly to engage endogenous cytoprotective processes. Hence, GRP78 may control either UPR and macroautophagy or may activated phosphatidylinositol 3-kinase (PI3K)/AKT pro-survival pathways. GRP78 influences how tumor cells survive, proliferate, and develop chemoresistance. In neurodegeneration, endogenous mechanisms of neuroprotection are frequently insufficient or dysregulated. Lessons from tumor biology may give us clues about how boosting endogenous neuroprotective mechanisms in age-related neurodegeneration. Herein, the functions of GRP78 are revealed at the center of the stage of apparently opposite sites of the same coin regarding cytoprotection: neurodegeneration and cancer. The goal is to give a comprehensive and critical review that may serve to guide future experiments to identify interventions that will enhance neuroprotection. Frontiers Media S.A. 2017-04-05 /pmc/articles/PMC5380735/ /pubmed/28424579 http://dx.doi.org/10.3389/fnins.2017.00177 Text en Copyright © 2017 Casas. 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 | Neuroscience Casas, Caty GRP78 at the Centre of the Stage in Cancer and Neuroprotection |
title | GRP78 at the Centre of the Stage in Cancer and Neuroprotection |
title_full | GRP78 at the Centre of the Stage in Cancer and Neuroprotection |
title_fullStr | GRP78 at the Centre of the Stage in Cancer and Neuroprotection |
title_full_unstemmed | GRP78 at the Centre of the Stage in Cancer and Neuroprotection |
title_short | GRP78 at the Centre of the Stage in Cancer and Neuroprotection |
title_sort | grp78 at the centre of the stage in cancer and neuroprotection |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380735/ https://www.ncbi.nlm.nih.gov/pubmed/28424579 http://dx.doi.org/10.3389/fnins.2017.00177 |
work_keys_str_mv | AT casascaty grp78atthecentreofthestageincancerandneuroprotection |