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Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?

Coronary heart disease (CHD) is the leading cause of death around the world. Based on the roles of vascular endothelial growth factor (VEGF) family members to regulate blood and lymphatic vessels and metabolic functions, several therapeutic approaches have been attempted during the last decade. Howe...

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Detalles Bibliográficos
Autores principales: Mallick, Rahul, Ylä-Herttuala, Seppo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776740/
https://www.ncbi.nlm.nih.gov/pubmed/36552897
http://dx.doi.org/10.3390/cells11244134
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author Mallick, Rahul
Ylä-Herttuala, Seppo
author_facet Mallick, Rahul
Ylä-Herttuala, Seppo
author_sort Mallick, Rahul
collection PubMed
description Coronary heart disease (CHD) is the leading cause of death around the world. Based on the roles of vascular endothelial growth factor (VEGF) family members to regulate blood and lymphatic vessels and metabolic functions, several therapeutic approaches have been attempted during the last decade. However proangiogenic therapies based on classical VEGF-A have been disappointing. Therefore, it has become important to focus on other VEGFs such as VEGF-B, which is a novel member of the VEGF family. Recent studies have shown the very promising potential of the VEGF-B to treat CHD and heart failure. The aim of this review article is to present the role of VEGF-B in endothelial biology and as a potential therapeutic agent for CHD and heart failure. In addition, key differences between the VEGF-A and VEGF-B effects on endothelial functions are demonstrated.
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spelling pubmed-97767402022-12-23 Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision? Mallick, Rahul Ylä-Herttuala, Seppo Cells Review Coronary heart disease (CHD) is the leading cause of death around the world. Based on the roles of vascular endothelial growth factor (VEGF) family members to regulate blood and lymphatic vessels and metabolic functions, several therapeutic approaches have been attempted during the last decade. However proangiogenic therapies based on classical VEGF-A have been disappointing. Therefore, it has become important to focus on other VEGFs such as VEGF-B, which is a novel member of the VEGF family. Recent studies have shown the very promising potential of the VEGF-B to treat CHD and heart failure. The aim of this review article is to present the role of VEGF-B in endothelial biology and as a potential therapeutic agent for CHD and heart failure. In addition, key differences between the VEGF-A and VEGF-B effects on endothelial functions are demonstrated. MDPI 2022-12-19 /pmc/articles/PMC9776740/ /pubmed/36552897 http://dx.doi.org/10.3390/cells11244134 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
Mallick, Rahul
Ylä-Herttuala, Seppo
Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?
title Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?
title_full Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?
title_fullStr Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?
title_full_unstemmed Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?
title_short Therapeutic Potential of VEGF-B in Coronary Heart Disease and Heart Failure: Dream or Vision?
title_sort therapeutic potential of vegf-b in coronary heart disease and heart failure: dream or vision?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776740/
https://www.ncbi.nlm.nih.gov/pubmed/36552897
http://dx.doi.org/10.3390/cells11244134
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