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Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review

Glucose-Regulated Protein 78 (GRP78) is a chaperone protein that is predominantly expressed in the lumen of the endoplasmic reticulum. GRP78 plays a crucial role in protein folding by assisting in the assembly of misfolded proteins. Under cellular stress conditions, GRP78 can translocate to the cell...

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Autores principales: Akinyemi, Amos Olalekan, Simpson, Kendall Elizabeth, Oyelere, Sunday Faith, Nur, Maria, Ngule, Chrispus Mutuku, Owoyemi, Bolaji Charles Dayo, Ayarick, Vivian Adiila, Oyelami, Felix Femi, Obaleye, Oluwafunminiyi, Esoe, Dave-Preston, Liu, Xiaoqi, Li, Zhiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464436/
https://www.ncbi.nlm.nih.gov/pubmed/37605113
http://dx.doi.org/10.1186/s10020-023-00706-6
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author Akinyemi, Amos Olalekan
Simpson, Kendall Elizabeth
Oyelere, Sunday Faith
Nur, Maria
Ngule, Chrispus Mutuku
Owoyemi, Bolaji Charles Dayo
Ayarick, Vivian Adiila
Oyelami, Felix Femi
Obaleye, Oluwafunminiyi
Esoe, Dave-Preston
Liu, Xiaoqi
Li, Zhiguo
author_facet Akinyemi, Amos Olalekan
Simpson, Kendall Elizabeth
Oyelere, Sunday Faith
Nur, Maria
Ngule, Chrispus Mutuku
Owoyemi, Bolaji Charles Dayo
Ayarick, Vivian Adiila
Oyelami, Felix Femi
Obaleye, Oluwafunminiyi
Esoe, Dave-Preston
Liu, Xiaoqi
Li, Zhiguo
author_sort Akinyemi, Amos Olalekan
collection PubMed
description Glucose-Regulated Protein 78 (GRP78) is a chaperone protein that is predominantly expressed in the lumen of the endoplasmic reticulum. GRP78 plays a crucial role in protein folding by assisting in the assembly of misfolded proteins. Under cellular stress conditions, GRP78 can translocate to the cell surface (csGRP78) were it interacts with different ligands to initiate various intracellular pathways. The expression of csGRP78 has been associated with tumor initiation and progression of multiple cancer types. This review provides a comprehensive analysis of the existing evidence on the roles of GRP78 in various types of cancer and other human pathology. Additionally, the review discusses the current understanding of the mechanisms underlying GRP78's involvement in tumorigenesis and cancer advancement. Furthermore, we highlight recent innovative approaches employed in downregulating GRP78 expression in cancers as a potential therapeutic target.
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spelling pubmed-104644362023-08-30 Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review Akinyemi, Amos Olalekan Simpson, Kendall Elizabeth Oyelere, Sunday Faith Nur, Maria Ngule, Chrispus Mutuku Owoyemi, Bolaji Charles Dayo Ayarick, Vivian Adiila Oyelami, Felix Femi Obaleye, Oluwafunminiyi Esoe, Dave-Preston Liu, Xiaoqi Li, Zhiguo Mol Med Review Glucose-Regulated Protein 78 (GRP78) is a chaperone protein that is predominantly expressed in the lumen of the endoplasmic reticulum. GRP78 plays a crucial role in protein folding by assisting in the assembly of misfolded proteins. Under cellular stress conditions, GRP78 can translocate to the cell surface (csGRP78) were it interacts with different ligands to initiate various intracellular pathways. The expression of csGRP78 has been associated with tumor initiation and progression of multiple cancer types. This review provides a comprehensive analysis of the existing evidence on the roles of GRP78 in various types of cancer and other human pathology. Additionally, the review discusses the current understanding of the mechanisms underlying GRP78's involvement in tumorigenesis and cancer advancement. Furthermore, we highlight recent innovative approaches employed in downregulating GRP78 expression in cancers as a potential therapeutic target. BioMed Central 2023-08-21 /pmc/articles/PMC10464436/ /pubmed/37605113 http://dx.doi.org/10.1186/s10020-023-00706-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Akinyemi, Amos Olalekan
Simpson, Kendall Elizabeth
Oyelere, Sunday Faith
Nur, Maria
Ngule, Chrispus Mutuku
Owoyemi, Bolaji Charles Dayo
Ayarick, Vivian Adiila
Oyelami, Felix Femi
Obaleye, Oluwafunminiyi
Esoe, Dave-Preston
Liu, Xiaoqi
Li, Zhiguo
Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review
title Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review
title_full Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review
title_fullStr Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review
title_full_unstemmed Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review
title_short Unveiling the dark side of glucose-regulated protein 78 (GRP78) in cancers and other human pathology: a systematic review
title_sort unveiling the dark side of glucose-regulated protein 78 (grp78) in cancers and other human pathology: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464436/
https://www.ncbi.nlm.nih.gov/pubmed/37605113
http://dx.doi.org/10.1186/s10020-023-00706-6
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