Charting the path: navigating embryonic development to potentially safeguard against congenital heart defects

Detalhes bibliográficos
Autor(a) principal: Bragança, José
Data de Publicação: 2023
Outros Autores: Pinto, Rute L., Silva, Barbara S., Marques, Nuno, Leitao, Helena, Fernandes, Mónica T.
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.
id RCAP_894e8ee50b1507077293c1d005492bd5
oai_identifier_str oai:sapientia.ualg.pt:10400.1/19977
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling 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
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv MDPI
publisher.none.fl_str_mv MDPI
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799133565366042624