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Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches
Regenerative medicine is a new therapeutic modality that aims to mend tissue damage by encouraging the reconstitution of physiological integrity. It represents an advancement over conventional therapies that allow reducing the damage but result in disease chronicization. Age-related decline in spont...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439942/ https://www.ncbi.nlm.nih.gov/pubmed/32923974 http://dx.doi.org/10.1530/VB-19-0029 |
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author | Magenta, Alessandra Lorde, Reggio Syed, Sunayana Begum Capogrossi, Maurizio C Puca, Annibale Madeddu, Paolo |
author_facet | Magenta, Alessandra Lorde, Reggio Syed, Sunayana Begum Capogrossi, Maurizio C Puca, Annibale Madeddu, Paolo |
author_sort | Magenta, Alessandra |
collection | PubMed |
description | Regenerative medicine is a new therapeutic modality that aims to mend tissue damage by encouraging the reconstitution of physiological integrity. It represents an advancement over conventional therapies that allow reducing the damage but result in disease chronicization. Age-related decline in spontaneous capacity of repair, especially in organs like the heart that have very limited proliferative capacity, contributes in reducing the benefit of conventional therapy. ncRNAs are emerging as key epigenetic regulators of cardiovascular regeneration. Inhibition or replacement of miRNAs may offer reparative solutions to cardiovascular disease. The first part of this review article is devoted to illustrating novel therapies emerging from research on miRNAs. In the second part, we develop new therapeutic concepts emerging from genetics of longevity. Prolonged survival, as in supercentenarians, denotes an exceptional capacity to repair and cope with risk factors and diseases. These characteristics are shared with offspring, suggesting that the regenerative phenotype is heritable. New evidence indicates that genetic traits responsible for prolongation of health span in humans can be passed to and benefit the outcomes of animal models of cardiovascular disease. Genetic studies have also focused on determinants of accelerated senescence and related druggable targets. Evolutionary genetics assessing the genetic basis of adaptation and comparing successful and unsuccessful genetic changes in response to selection within populations represent a powerful basis to develop novel therapies aiming to prolong cardiovascular and whole organism health. |
format | Online Article Text |
id | pubmed-7439942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-74399422020-09-10 Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches Magenta, Alessandra Lorde, Reggio Syed, Sunayana Begum Capogrossi, Maurizio C Puca, Annibale Madeddu, Paolo Vasc Biol Review Regenerative medicine is a new therapeutic modality that aims to mend tissue damage by encouraging the reconstitution of physiological integrity. It represents an advancement over conventional therapies that allow reducing the damage but result in disease chronicization. Age-related decline in spontaneous capacity of repair, especially in organs like the heart that have very limited proliferative capacity, contributes in reducing the benefit of conventional therapy. ncRNAs are emerging as key epigenetic regulators of cardiovascular regeneration. Inhibition or replacement of miRNAs may offer reparative solutions to cardiovascular disease. The first part of this review article is devoted to illustrating novel therapies emerging from research on miRNAs. In the second part, we develop new therapeutic concepts emerging from genetics of longevity. Prolonged survival, as in supercentenarians, denotes an exceptional capacity to repair and cope with risk factors and diseases. These characteristics are shared with offspring, suggesting that the regenerative phenotype is heritable. New evidence indicates that genetic traits responsible for prolongation of health span in humans can be passed to and benefit the outcomes of animal models of cardiovascular disease. Genetic studies have also focused on determinants of accelerated senescence and related druggable targets. Evolutionary genetics assessing the genetic basis of adaptation and comparing successful and unsuccessful genetic changes in response to selection within populations represent a powerful basis to develop novel therapies aiming to prolong cardiovascular and whole organism health. Bioscientifica Ltd 2020-01-16 /pmc/articles/PMC7439942/ /pubmed/32923974 http://dx.doi.org/10.1530/VB-19-0029 Text en © 2020 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Review Magenta, Alessandra Lorde, Reggio Syed, Sunayana Begum Capogrossi, Maurizio C Puca, Annibale Madeddu, Paolo Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
title | Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
title_full | Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
title_fullStr | Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
title_full_unstemmed | Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
title_short | Molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
title_sort | molecular therapies delaying cardiovascular aging: disease- or health-oriented approaches |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439942/ https://www.ncbi.nlm.nih.gov/pubmed/32923974 http://dx.doi.org/10.1530/VB-19-0029 |
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