Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.1/19977 |
Resumo: | Congenital heart diseases (CHDs) are structural or functional defects present at birth due to improper heart development. Current therapeutic approaches to treating severe CHDs are primarily palliative surgical interventions during the peri- or prenatal stages, when the heart has fully developed from faulty embryogenesis. However, earlier interventions during embryonic development have the potential for better outcomes, as demonstrated by fetal cardiac interventions performed in utero, which have shown improved neonatal and prenatal survival rates, as well as reduced lifelong morbidity. Extensive research on heart development has identified key steps, cellular players, and the intricate network of signaling pathways and transcription factors governing cardiogenesis. Additionally, some reports have indicated that certain adverse genetic and environmental conditions leading to heart malformations and embryonic death may be amendable through the activation of alternative mechanisms. This review first highlights key molecular and cellular processes involved in heart development. Subsequently, it explores the potential for future therapeutic strategies, targeting early embryonic stages, to prevent CHDs, through the delivery of biomolecules or exosomes to compensate for faulty cardiogenic mechanisms. Implementing such non-surgical interventions during early gestation may offer a prophylactic approach toward reducing the occurrence and severity of CHDs. |
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Charting the path: navigating embryonic development to potentially safeguard against congenital heart defectsStem cellsPlacenta and heart developmentCongenital heart diseasesSecretomesExosomeBlastocystCardiogenic signaling pathwaysCongenital heart diseases (CHDs) are structural or functional defects present at birth due to improper heart development. Current therapeutic approaches to treating severe CHDs are primarily palliative surgical interventions during the peri- or prenatal stages, when the heart has fully developed from faulty embryogenesis. However, earlier interventions during embryonic development have the potential for better outcomes, as demonstrated by fetal cardiac interventions performed in utero, which have shown improved neonatal and prenatal survival rates, as well as reduced lifelong morbidity. Extensive research on heart development has identified key steps, cellular players, and the intricate network of signaling pathways and transcription factors governing cardiogenesis. Additionally, some reports have indicated that certain adverse genetic and environmental conditions leading to heart malformations and embryonic death may be amendable through the activation of alternative mechanisms. This review first highlights key molecular and cellular processes involved in heart development. Subsequently, it explores the potential for future therapeutic strategies, targeting early embryonic stages, to prevent CHDs, through the delivery of biomolecules or exosomes to compensate for faulty cardiogenic mechanisms. Implementing such non-surgical interventions during early gestation may offer a prophylactic approach toward reducing the occurrence and severity of CHDs.ALG-45-2020-41; 2022.13253.BDANAMDPISapientiaBragança, JoséPinto, Rute L.Silva, Barbara S.Marques, NunoLeitao, HelenaFernandes, Mónica T.2023-09-13T12:19:24Z2023-08-152023-08-25T12:38:15Z2023-08-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/19977engJournal of Personalized Medicine 13 (8): 1263 (2023)2075-442610.3390/jpm13081263info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-09-20T02:00:32Zoai:sapientia.ualg.pt:10400.1/19977Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:29:42.973819Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
title |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
spellingShingle |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects Bragança, José Stem cells Placenta and heart development Congenital heart diseases Secretomes Exosome Blastocyst Cardiogenic signaling pathways |
title_short |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
title_full |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
title_fullStr |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
title_full_unstemmed |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
title_sort |
Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects |
author |
Bragança, José |
author_facet |
Bragança, José Pinto, Rute L. Silva, Barbara S. Marques, Nuno Leitao, Helena Fernandes, Mónica T. |
author_role |
author |
author2 |
Pinto, Rute L. Silva, Barbara S. Marques, Nuno Leitao, Helena Fernandes, Mónica T. |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Sapientia |
dc.contributor.author.fl_str_mv |
Bragança, José Pinto, Rute L. Silva, Barbara S. Marques, Nuno Leitao, Helena Fernandes, Mónica T. |
dc.subject.por.fl_str_mv |
Stem cells Placenta and heart development Congenital heart diseases Secretomes Exosome Blastocyst Cardiogenic signaling pathways |
topic |
Stem cells Placenta and heart development Congenital heart diseases Secretomes Exosome Blastocyst Cardiogenic signaling pathways |
description |
Congenital heart diseases (CHDs) are structural or functional defects present at birth due to improper heart development. Current therapeutic approaches to treating severe CHDs are primarily palliative surgical interventions during the peri- or prenatal stages, when the heart has fully developed from faulty embryogenesis. However, earlier interventions during embryonic development have the potential for better outcomes, as demonstrated by fetal cardiac interventions performed in utero, which have shown improved neonatal and prenatal survival rates, as well as reduced lifelong morbidity. Extensive research on heart development has identified key steps, cellular players, and the intricate network of signaling pathways and transcription factors governing cardiogenesis. Additionally, some reports have indicated that certain adverse genetic and environmental conditions leading to heart malformations and embryonic death may be amendable through the activation of alternative mechanisms. This review first highlights key molecular and cellular processes involved in heart development. Subsequently, it explores the potential for future therapeutic strategies, targeting early embryonic stages, to prevent CHDs, through the delivery of biomolecules or exosomes to compensate for faulty cardiogenic mechanisms. Implementing such non-surgical interventions during early gestation may offer a prophylactic approach toward reducing the occurrence and severity of CHDs. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-09-13T12:19:24Z 2023-08-15 2023-08-25T12:38:15Z 2023-08-15T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.1/19977 |
url |
http://hdl.handle.net/10400.1/19977 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Personalized Medicine 13 (8): 1263 (2023) 2075-4426 10.3390/jpm13081263 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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application/pdf |
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MDPI |
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MDPI |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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