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GRP78: A cell's response to stress

BACKGROUND: Glucose-Regulated Protein 78 (GRP78) is a chaperone heat shock protein that has been intensely studied in the last two decades. GRP78 is the master of the unfolded protein response (UBR) in the Endoplasmic Reticulum (ER) in normal cells. GRP78 force the unfolded proteins to refold or deg...

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Detalles Bibliográficos
Autores principales: Ibrahim, Ibrahim M., Abdelmalek, Doaa H., Elfiky, Abdo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094232/
https://www.ncbi.nlm.nih.gov/pubmed/30978349
http://dx.doi.org/10.1016/j.lfs.2019.04.022
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author Ibrahim, Ibrahim M.
Abdelmalek, Doaa H.
Elfiky, Abdo A.
author_facet Ibrahim, Ibrahim M.
Abdelmalek, Doaa H.
Elfiky, Abdo A.
author_sort Ibrahim, Ibrahim M.
collection PubMed
description BACKGROUND: Glucose-Regulated Protein 78 (GRP78) is a chaperone heat shock protein that has been intensely studied in the last two decades. GRP78 is the master of the unfolded protein response (UBR) in the Endoplasmic Reticulum (ER) in normal cells. GRP78 force the unfolded proteins to refold or degrade using cellular degradation mechanisms. SCOPE: Under stress, the overexpression of GRP78 on the cell membrane mediates the vast amount of disordered proteins. Unfortunately, this makes it a tool for pathogens (bacterial, fungal and viral) to enter the cell and to start different pathways leading to pathogenesis. Additionally, GRP78 is overexpressed on the membranes of various cancer cells and increase the aggressiveness of the disease. MAJOR CONCLUSIONS: The current review summarizes structure, function, and different mechanisms GRP78 mediate in response to normal or stress conditions. GENERAL SIGNIFICANCE: GRP78 targeting and possible inhibition mechanisms are also covered in the present review aiming to prevent the virulence of pathogens and cancer.
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spelling pubmed-70942322020-03-25 GRP78: A cell's response to stress Ibrahim, Ibrahim M. Abdelmalek, Doaa H. Elfiky, Abdo A. Life Sci Review Article BACKGROUND: Glucose-Regulated Protein 78 (GRP78) is a chaperone heat shock protein that has been intensely studied in the last two decades. GRP78 is the master of the unfolded protein response (UBR) in the Endoplasmic Reticulum (ER) in normal cells. GRP78 force the unfolded proteins to refold or degrade using cellular degradation mechanisms. SCOPE: Under stress, the overexpression of GRP78 on the cell membrane mediates the vast amount of disordered proteins. Unfortunately, this makes it a tool for pathogens (bacterial, fungal and viral) to enter the cell and to start different pathways leading to pathogenesis. Additionally, GRP78 is overexpressed on the membranes of various cancer cells and increase the aggressiveness of the disease. MAJOR CONCLUSIONS: The current review summarizes structure, function, and different mechanisms GRP78 mediate in response to normal or stress conditions. GENERAL SIGNIFICANCE: GRP78 targeting and possible inhibition mechanisms are also covered in the present review aiming to prevent the virulence of pathogens and cancer. Elsevier Inc. 2019-06-01 2019-04-09 /pmc/articles/PMC7094232/ /pubmed/30978349 http://dx.doi.org/10.1016/j.lfs.2019.04.022 Text en © 2019 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review Article
Ibrahim, Ibrahim M.
Abdelmalek, Doaa H.
Elfiky, Abdo A.
GRP78: A cell's response to stress
title GRP78: A cell's response to stress
title_full GRP78: A cell's response to stress
title_fullStr GRP78: A cell's response to stress
title_full_unstemmed GRP78: A cell's response to stress
title_short GRP78: A cell's response to stress
title_sort grp78: a cell's response to stress
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094232/
https://www.ncbi.nlm.nih.gov/pubmed/30978349
http://dx.doi.org/10.1016/j.lfs.2019.04.022
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