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The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective
Vascular calcification (VC) is an important complication among patients of advanced age, those with chronic kidney disease, and those with diabetes mellitus. The pathophysiology of VC encompasses passive occurrence of physico-chemical calcium deposition, active cellular secretion of osteoid matrix u...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037112/ https://www.ncbi.nlm.nih.gov/pubmed/32024140 http://dx.doi.org/10.3390/ijms21030980 |
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author | Hou, Yi-Chou Lu, Chien-Lin Yuan, Tzu-Hang Liao, Min-Tser Chao, Chia-Ter Lu, Kuo-Cheng |
author_facet | Hou, Yi-Chou Lu, Chien-Lin Yuan, Tzu-Hang Liao, Min-Tser Chao, Chia-Ter Lu, Kuo-Cheng |
author_sort | Hou, Yi-Chou |
collection | PubMed |
description | Vascular calcification (VC) is an important complication among patients of advanced age, those with chronic kidney disease, and those with diabetes mellitus. The pathophysiology of VC encompasses passive occurrence of physico-chemical calcium deposition, active cellular secretion of osteoid matrix upon exposure to metabolically noxious stimuli, or a variable combination of both processes. Epigenetic alterations have been shown to participate in this complex environment, through mechanisms including DNA methylation, non-coding RNAs, histone modifications, and chromatin changes. Despite such importance, existing reviews fail to provide a comprehensive view of all relevant reports addressing epigenetic processes in VC, and cross-talk between different epigenetic machineries is rarely examined. We conducted a systematic review based on PUBMED and MEDLINE databases up to 30 September 2019, to identify clinical, translational, and experimental reports addressing epigenetic processes in VC; we retrieved 66 original studies, among which 60.6% looked into the pathogenic role of non-coding RNA, followed by DNA methylation (12.1%), histone modification (9.1%), and chromatin changes (4.5%). Nine (13.6%) reports examined the discrepancy of epigenetic signatures between subjects or tissues with and without VC, supporting their applicability as biomarkers. Assisted by bioinformatic analyses blending in each epigenetic component, we discovered prominent interactions between microRNAs, DNA methylation, and histone modification regarding potential influences on VC risk. |
format | Online Article Text |
id | pubmed-7037112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70371122020-03-11 The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective Hou, Yi-Chou Lu, Chien-Lin Yuan, Tzu-Hang Liao, Min-Tser Chao, Chia-Ter Lu, Kuo-Cheng Int J Mol Sci Review Vascular calcification (VC) is an important complication among patients of advanced age, those with chronic kidney disease, and those with diabetes mellitus. The pathophysiology of VC encompasses passive occurrence of physico-chemical calcium deposition, active cellular secretion of osteoid matrix upon exposure to metabolically noxious stimuli, or a variable combination of both processes. Epigenetic alterations have been shown to participate in this complex environment, through mechanisms including DNA methylation, non-coding RNAs, histone modifications, and chromatin changes. Despite such importance, existing reviews fail to provide a comprehensive view of all relevant reports addressing epigenetic processes in VC, and cross-talk between different epigenetic machineries is rarely examined. We conducted a systematic review based on PUBMED and MEDLINE databases up to 30 September 2019, to identify clinical, translational, and experimental reports addressing epigenetic processes in VC; we retrieved 66 original studies, among which 60.6% looked into the pathogenic role of non-coding RNA, followed by DNA methylation (12.1%), histone modification (9.1%), and chromatin changes (4.5%). Nine (13.6%) reports examined the discrepancy of epigenetic signatures between subjects or tissues with and without VC, supporting their applicability as biomarkers. Assisted by bioinformatic analyses blending in each epigenetic component, we discovered prominent interactions between microRNAs, DNA methylation, and histone modification regarding potential influences on VC risk. MDPI 2020-02-01 /pmc/articles/PMC7037112/ /pubmed/32024140 http://dx.doi.org/10.3390/ijms21030980 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hou, Yi-Chou Lu, Chien-Lin Yuan, Tzu-Hang Liao, Min-Tser Chao, Chia-Ter Lu, Kuo-Cheng The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective |
title | The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective |
title_full | The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective |
title_fullStr | The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective |
title_full_unstemmed | The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective |
title_short | The Epigenetic Landscape of Vascular Calcification: An Integrative Perspective |
title_sort | epigenetic landscape of vascular calcification: an integrative perspective |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037112/ https://www.ncbi.nlm.nih.gov/pubmed/32024140 http://dx.doi.org/10.3390/ijms21030980 |
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