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Targeting the GRP78 Pathway for Cancer Therapy
The 78-kDa glucose-regulated protein (GRP78) plays an important part in maintaining protein stability, regulating protein folding, and inducing apoptosis autophagy, which is considered as a powerful protein. Meanwhile, it also plays a role in ensuring the normal function of organs. In recent years,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409388/ https://www.ncbi.nlm.nih.gov/pubmed/32850882 http://dx.doi.org/10.3389/fmed.2020.00351 |
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author | Lu, Guanhua Luo, Hui Zhu, Xiao |
author_facet | Lu, Guanhua Luo, Hui Zhu, Xiao |
author_sort | Lu, Guanhua |
collection | PubMed |
description | The 78-kDa glucose-regulated protein (GRP78) plays an important part in maintaining protein stability, regulating protein folding, and inducing apoptosis autophagy, which is considered as a powerful protein. Meanwhile, it also plays a role in ensuring the normal function of organs. In recent years, more and more researches have been carried out on the targeted therapy of GRP78, mainly focusing on its relevant role in tumor and its role as a major modulator and modulator of subordinate pathways. The ability of GRP78 to respond to endoplasmic reticulum stress (ERS) determines whether tumor cells survive and whether the changes in expression level of GRP78 regulated by endoplasmic reticulum (ER) caused by various factors will directly or indirectly affect cell proliferation, apoptosis, and injury, or reduce the body's defense ability, or have protective effects on various organs. |
format | Online Article Text |
id | pubmed-7409388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74093882020-08-25 Targeting the GRP78 Pathway for Cancer Therapy Lu, Guanhua Luo, Hui Zhu, Xiao Front Med (Lausanne) Medicine The 78-kDa glucose-regulated protein (GRP78) plays an important part in maintaining protein stability, regulating protein folding, and inducing apoptosis autophagy, which is considered as a powerful protein. Meanwhile, it also plays a role in ensuring the normal function of organs. In recent years, more and more researches have been carried out on the targeted therapy of GRP78, mainly focusing on its relevant role in tumor and its role as a major modulator and modulator of subordinate pathways. The ability of GRP78 to respond to endoplasmic reticulum stress (ERS) determines whether tumor cells survive and whether the changes in expression level of GRP78 regulated by endoplasmic reticulum (ER) caused by various factors will directly or indirectly affect cell proliferation, apoptosis, and injury, or reduce the body's defense ability, or have protective effects on various organs. Frontiers Media S.A. 2020-07-30 /pmc/articles/PMC7409388/ /pubmed/32850882 http://dx.doi.org/10.3389/fmed.2020.00351 Text en Copyright © 2020 Lu, Luo and Zhu. 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) and the copyright owner(s) 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 | Medicine Lu, Guanhua Luo, Hui Zhu, Xiao Targeting the GRP78 Pathway for Cancer Therapy |
title | Targeting the GRP78 Pathway for Cancer Therapy |
title_full | Targeting the GRP78 Pathway for Cancer Therapy |
title_fullStr | Targeting the GRP78 Pathway for Cancer Therapy |
title_full_unstemmed | Targeting the GRP78 Pathway for Cancer Therapy |
title_short | Targeting the GRP78 Pathway for Cancer Therapy |
title_sort | targeting the grp78 pathway for cancer therapy |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409388/ https://www.ncbi.nlm.nih.gov/pubmed/32850882 http://dx.doi.org/10.3389/fmed.2020.00351 |
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