The impact of long noncoding RNAs in tissue regeneration and senescence

Bibliographic Details
Main Author: Silva, Júlia Tavares e
Publication Date: 2024
Other Authors: Pessoa, João, Nóbrega-Pereira, Sandrina, Jesus, Bruno Bernardes de
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10773/43450
Summary: Overcoming senescence with tissue engineering has a promising impact on multiple diseases. Here, we provide an overview of recent studies in which cellular senescence was inhibited through the up/downregulation of specific lncRNAs. This approach prevented senescence in the bones, joints, nervous system, heart, and blood vessels, with a potential impact on regeneration and the prevention of osteoarthritis and osteoporosis, as well as neurodegenerative and cardiovascular diseases. Senescence of the skin and liver could also be prevented through the regulation of cellular levels of specific lncRNAs, resulting in the rejuvenation of cells from these organs and their potential protection from disease. From these exciting achievements, which support tissue regeneration and are not restricted to stem cells, we propose lncRNA regulation through RNA or gene therapies as a prospective preventive and therapeutic approach against aging and multiple aging-related diseases.
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spelling The impact of long noncoding RNAs in tissue regeneration and senescenceAgingCellular senescenceLong noncoding RNAsUpregulationDownregulationNeurodegenerationCardiovascular diseaseOvercoming senescence with tissue engineering has a promising impact on multiple diseases. Here, we provide an overview of recent studies in which cellular senescence was inhibited through the up/downregulation of specific lncRNAs. This approach prevented senescence in the bones, joints, nervous system, heart, and blood vessels, with a potential impact on regeneration and the prevention of osteoarthritis and osteoporosis, as well as neurodegenerative and cardiovascular diseases. Senescence of the skin and liver could also be prevented through the regulation of cellular levels of specific lncRNAs, resulting in the rejuvenation of cells from these organs and their potential protection from disease. From these exciting achievements, which support tissue regeneration and are not restricted to stem cells, we propose lncRNA regulation through RNA or gene therapies as a prospective preventive and therapeutic approach against aging and multiple aging-related diseases.MDPI2025-01-15T17:48:02Z2024-01-09T00:00:00Z2024-01-09info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/43450eng10.3390/cells13020119Silva, Júlia Tavares ePessoa, JoãoNóbrega-Pereira, SandrinaJesus, Bruno Bernardes deinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-01-20T01:48:13Zoai:ria.ua.pt:10773/43450Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T19:40:34.125483Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv The impact of long noncoding RNAs in tissue regeneration and senescence
title The impact of long noncoding RNAs in tissue regeneration and senescence
spellingShingle The impact of long noncoding RNAs in tissue regeneration and senescence
Silva, Júlia Tavares e
Aging
Cellular senescence
Long noncoding RNAs
Upregulation
Downregulation
Neurodegeneration
Cardiovascular disease
title_short The impact of long noncoding RNAs in tissue regeneration and senescence
title_full The impact of long noncoding RNAs in tissue regeneration and senescence
title_fullStr The impact of long noncoding RNAs in tissue regeneration and senescence
title_full_unstemmed The impact of long noncoding RNAs in tissue regeneration and senescence
title_sort The impact of long noncoding RNAs in tissue regeneration and senescence
author Silva, Júlia Tavares e
author_facet Silva, Júlia Tavares e
Pessoa, João
Nóbrega-Pereira, Sandrina
Jesus, Bruno Bernardes de
author_role author
author2 Pessoa, João
Nóbrega-Pereira, Sandrina
Jesus, Bruno Bernardes de
author2_role author
author
author
dc.contributor.author.fl_str_mv Silva, Júlia Tavares e
Pessoa, João
Nóbrega-Pereira, Sandrina
Jesus, Bruno Bernardes de
dc.subject.por.fl_str_mv Aging
Cellular senescence
Long noncoding RNAs
Upregulation
Downregulation
Neurodegeneration
Cardiovascular disease
topic Aging
Cellular senescence
Long noncoding RNAs
Upregulation
Downregulation
Neurodegeneration
Cardiovascular disease
description Overcoming senescence with tissue engineering has a promising impact on multiple diseases. Here, we provide an overview of recent studies in which cellular senescence was inhibited through the up/downregulation of specific lncRNAs. This approach prevented senescence in the bones, joints, nervous system, heart, and blood vessels, with a potential impact on regeneration and the prevention of osteoarthritis and osteoporosis, as well as neurodegenerative and cardiovascular diseases. Senescence of the skin and liver could also be prevented through the regulation of cellular levels of specific lncRNAs, resulting in the rejuvenation of cells from these organs and their potential protection from disease. From these exciting achievements, which support tissue regeneration and are not restricted to stem cells, we propose lncRNA regulation through RNA or gene therapies as a prospective preventive and therapeutic approach against aging and multiple aging-related diseases.
publishDate 2024
dc.date.none.fl_str_mv 2024-01-09T00:00:00Z
2024-01-09
2025-01-15T17:48:02Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/43450
url http://hdl.handle.net/10773/43450
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.3390/cells13020119
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