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Targeting MicroRNA Function in Acute Pancreatitis
Acute pancreatitis (AP) is a common gastrointestinal disorder that featured by acute inflammatory responses leading to systemic inflammatory response syndrome (SIRS) or multiple organ failure. A worldwide increase in annual incidence has been observed during the past decade with high acute hospitali...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613139/ https://www.ncbi.nlm.nih.gov/pubmed/28983256 http://dx.doi.org/10.3389/fphys.2017.00726 |
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author | Xiang, Hong Tao, Xufeng Xia, Shilin Qu, Jialin Song, Huiyi Liu, Jianjun Shang, Dong |
author_facet | Xiang, Hong Tao, Xufeng Xia, Shilin Qu, Jialin Song, Huiyi Liu, Jianjun Shang, Dong |
author_sort | Xiang, Hong |
collection | PubMed |
description | Acute pancreatitis (AP) is a common gastrointestinal disorder that featured by acute inflammatory responses leading to systemic inflammatory response syndrome (SIRS) or multiple organ failure. A worldwide increase in annual incidence has been observed during the past decade with high acute hospitalization and mortality. Lack of any specific treatment for AP, even to this day, is a reminder that there is much to be learned about the exact pathogenesis of AP. Fortunately, the discovery of microRNA (miRNA) has started an entirely new thought process regarding the molecular mechanism associated with the disease processes. Given the extensive effort made on miRNA research, certain types of miRNA have been identified across a variety of biological processes, including cell differentiation, apoptosis, metabolism, and inflammatory responses. Mutations in miRNA sequences or deregulation of miRNA expression may contribute to the alteration of a pivotal physiological function leading to AP. Designing miRNA-related tools for AP diagnosis and treatment presents a novel and potential research frontier. In this mini-review, we summarize the current knowledge of various miRNAs closely interacting with AP and the possible development of targeted miRNA therapies in this disease, which may benefit the development of potential disease biomarkers and novel treatment targets for future medical implications. |
format | Online Article Text |
id | pubmed-5613139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56131392017-10-05 Targeting MicroRNA Function in Acute Pancreatitis Xiang, Hong Tao, Xufeng Xia, Shilin Qu, Jialin Song, Huiyi Liu, Jianjun Shang, Dong Front Physiol Physiology Acute pancreatitis (AP) is a common gastrointestinal disorder that featured by acute inflammatory responses leading to systemic inflammatory response syndrome (SIRS) or multiple organ failure. A worldwide increase in annual incidence has been observed during the past decade with high acute hospitalization and mortality. Lack of any specific treatment for AP, even to this day, is a reminder that there is much to be learned about the exact pathogenesis of AP. Fortunately, the discovery of microRNA (miRNA) has started an entirely new thought process regarding the molecular mechanism associated with the disease processes. Given the extensive effort made on miRNA research, certain types of miRNA have been identified across a variety of biological processes, including cell differentiation, apoptosis, metabolism, and inflammatory responses. Mutations in miRNA sequences or deregulation of miRNA expression may contribute to the alteration of a pivotal physiological function leading to AP. Designing miRNA-related tools for AP diagnosis and treatment presents a novel and potential research frontier. In this mini-review, we summarize the current knowledge of various miRNAs closely interacting with AP and the possible development of targeted miRNA therapies in this disease, which may benefit the development of potential disease biomarkers and novel treatment targets for future medical implications. Frontiers Media S.A. 2017-09-21 /pmc/articles/PMC5613139/ /pubmed/28983256 http://dx.doi.org/10.3389/fphys.2017.00726 Text en Copyright © 2017 Xiang, Tao, Xia, Qu, Song, Liu and Shang. 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 | Physiology Xiang, Hong Tao, Xufeng Xia, Shilin Qu, Jialin Song, Huiyi Liu, Jianjun Shang, Dong Targeting MicroRNA Function in Acute Pancreatitis |
title | Targeting MicroRNA Function in Acute Pancreatitis |
title_full | Targeting MicroRNA Function in Acute Pancreatitis |
title_fullStr | Targeting MicroRNA Function in Acute Pancreatitis |
title_full_unstemmed | Targeting MicroRNA Function in Acute Pancreatitis |
title_short | Targeting MicroRNA Function in Acute Pancreatitis |
title_sort | targeting microrna function in acute pancreatitis |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613139/ https://www.ncbi.nlm.nih.gov/pubmed/28983256 http://dx.doi.org/10.3389/fphys.2017.00726 |
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