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Understanding Necroptosis in Pancreatic Diseases
Intermediate between apoptosis and necrosis, necroptosis is a regulated caspase-independent programmed cell death that induces an inflammatory response and mediates cancer development. As our understanding improves, its role in the physiopathology of numerous diseases, including pancreatic diseases,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221205/ https://www.ncbi.nlm.nih.gov/pubmed/35740953 http://dx.doi.org/10.3390/biom12060828 |
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author | He, Ru Wang, Zhengfeng Dong, Shi Chen, Zhou Zhou, Wence |
author_facet | He, Ru Wang, Zhengfeng Dong, Shi Chen, Zhou Zhou, Wence |
author_sort | He, Ru |
collection | PubMed |
description | Intermediate between apoptosis and necrosis, necroptosis is a regulated caspase-independent programmed cell death that induces an inflammatory response and mediates cancer development. As our understanding improves, its role in the physiopathology of numerous diseases, including pancreatic diseases, has been reconsidered, and especially in pancreatitis and pancreatic cancer. However, the exact pathogenesis remains elusive, even though some studies have been conducted on these diseases. Its unique mechanisms of action in diseases are expected to bring prospects for the treatment of pancreatic diseases. Therefore, it is imperative to further explore its molecular mechanism in pancreatic diseases in order to identify novel therapeutic options. This article introduces recent related research on necroptosis and pancreatic diseases, explores necroptosis-related molecular pathways, and provides a theoretical foundation for new therapeutic targets for pancreatic diseases. |
format | Online Article Text |
id | pubmed-9221205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92212052022-06-24 Understanding Necroptosis in Pancreatic Diseases He, Ru Wang, Zhengfeng Dong, Shi Chen, Zhou Zhou, Wence Biomolecules Review Intermediate between apoptosis and necrosis, necroptosis is a regulated caspase-independent programmed cell death that induces an inflammatory response and mediates cancer development. As our understanding improves, its role in the physiopathology of numerous diseases, including pancreatic diseases, has been reconsidered, and especially in pancreatitis and pancreatic cancer. However, the exact pathogenesis remains elusive, even though some studies have been conducted on these diseases. Its unique mechanisms of action in diseases are expected to bring prospects for the treatment of pancreatic diseases. Therefore, it is imperative to further explore its molecular mechanism in pancreatic diseases in order to identify novel therapeutic options. This article introduces recent related research on necroptosis and pancreatic diseases, explores necroptosis-related molecular pathways, and provides a theoretical foundation for new therapeutic targets for pancreatic diseases. MDPI 2022-06-13 /pmc/articles/PMC9221205/ /pubmed/35740953 http://dx.doi.org/10.3390/biom12060828 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review He, Ru Wang, Zhengfeng Dong, Shi Chen, Zhou Zhou, Wence Understanding Necroptosis in Pancreatic Diseases |
title | Understanding Necroptosis in Pancreatic Diseases |
title_full | Understanding Necroptosis in Pancreatic Diseases |
title_fullStr | Understanding Necroptosis in Pancreatic Diseases |
title_full_unstemmed | Understanding Necroptosis in Pancreatic Diseases |
title_short | Understanding Necroptosis in Pancreatic Diseases |
title_sort | understanding necroptosis in pancreatic diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221205/ https://www.ncbi.nlm.nih.gov/pubmed/35740953 http://dx.doi.org/10.3390/biom12060828 |
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