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Cathepsins: a new culprit behind abdominal aortic aneurysm

Abdominal aortic aneurysm (AAA) is a fatal disease defined as an abdominal aortic diameter of 3.0 cm or more, where the abdominal aorta exceeds the normal diameter by more than 50%. Histopathological changes of AAA mainly include extracellular matrix (ECM) remodeling at the abdominal aorta wall, but...

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Detalles Bibliográficos
Autores principales: Wang, Yi, Tang, Chaoshu, Qin, Yanwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431531/
https://www.ncbi.nlm.nih.gov/pubmed/25984324
http://dx.doi.org/10.1186/2050-490X-1-5
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author Wang, Yi
Tang, Chaoshu
Qin, Yanwen
author_facet Wang, Yi
Tang, Chaoshu
Qin, Yanwen
author_sort Wang, Yi
collection PubMed
description Abdominal aortic aneurysm (AAA) is a fatal disease defined as an abdominal aortic diameter of 3.0 cm or more, where the abdominal aorta exceeds the normal diameter by more than 50%. Histopathological changes of AAA mainly include extracellular matrix (ECM) remodeling at the abdominal aorta wall, but there is lack of specific drugs to treat AAA. Recent studies have reported that lysosomal cathepsins could induce vascular remodeling and AAA formation by regulating vascular inflammation, medial smooth muscle cell apoptosis, neovascularization, and protease expression. Thus, cathepsins are expected to become a new therapeutic target for AAA treatment.
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spelling pubmed-44315312015-05-16 Cathepsins: a new culprit behind abdominal aortic aneurysm Wang, Yi Tang, Chaoshu Qin, Yanwen Regen Med Res Review Abdominal aortic aneurysm (AAA) is a fatal disease defined as an abdominal aortic diameter of 3.0 cm or more, where the abdominal aorta exceeds the normal diameter by more than 50%. Histopathological changes of AAA mainly include extracellular matrix (ECM) remodeling at the abdominal aorta wall, but there is lack of specific drugs to treat AAA. Recent studies have reported that lysosomal cathepsins could induce vascular remodeling and AAA formation by regulating vascular inflammation, medial smooth muscle cell apoptosis, neovascularization, and protease expression. Thus, cathepsins are expected to become a new therapeutic target for AAA treatment. BioMed Central 2013-11-01 /pmc/articles/PMC4431531/ /pubmed/25984324 http://dx.doi.org/10.1186/2050-490X-1-5 Text en © Wang et al.; licensee BioMed Central Ltd. 2013 This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Wang, Yi
Tang, Chaoshu
Qin, Yanwen
Cathepsins: a new culprit behind abdominal aortic aneurysm
title Cathepsins: a new culprit behind abdominal aortic aneurysm
title_full Cathepsins: a new culprit behind abdominal aortic aneurysm
title_fullStr Cathepsins: a new culprit behind abdominal aortic aneurysm
title_full_unstemmed Cathepsins: a new culprit behind abdominal aortic aneurysm
title_short Cathepsins: a new culprit behind abdominal aortic aneurysm
title_sort cathepsins: a new culprit behind abdominal aortic aneurysm
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431531/
https://www.ncbi.nlm.nih.gov/pubmed/25984324
http://dx.doi.org/10.1186/2050-490X-1-5
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AT tangchaoshu cathepsinsanewculpritbehindabdominalaorticaneurysm
AT qinyanwen cathepsinsanewculpritbehindabdominalaorticaneurysm