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Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy

Diabetic retinopathy (DR) is a severe complication of diabetes; however, its mechanism is not fully understood. Evidence has recently revealed that long non-coding RNAs (lncRNAs) are abnormally expressed in DR, and lncRNAs may function as pivotal regulators. LncRNAs are able to modulate gene express...

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Detalles Bibliográficos
Autores principales: Song, Zhaoxia, He, Chang, Wen, Jianping, Yang, Jianli, Chen, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875540/
https://www.ncbi.nlm.nih.gov/pubmed/36777876
http://dx.doi.org/10.2174/1389202923666220531105035
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author Song, Zhaoxia
He, Chang
Wen, Jianping
Yang, Jianli
Chen, Peng
author_facet Song, Zhaoxia
He, Chang
Wen, Jianping
Yang, Jianli
Chen, Peng
author_sort Song, Zhaoxia
collection PubMed
description Diabetic retinopathy (DR) is a severe complication of diabetes; however, its mechanism is not fully understood. Evidence has recently revealed that long non-coding RNAs (lncRNAs) are abnormally expressed in DR, and lncRNAs may function as pivotal regulators. LncRNAs are able to modulate gene expression at the epigenetic level by acting as scaffolds of histone modification complexes and sponges of binding with microRNAs (miRNAs). LncRNAs are believed to be important epigenetic regulators, which may become beneficial in the diagnosis and therapy of DR. However, the mechanisms of lncRNAs in DR are still unclear. In this review, we summarize the possible functions and mechanisms of lncRNAs in epigenetic regulation to target genes in the progression of DR.
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spelling pubmed-98755402023-02-11 Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy Song, Zhaoxia He, Chang Wen, Jianping Yang, Jianli Chen, Peng Curr Genomics Genetics & Genomics Diabetic retinopathy (DR) is a severe complication of diabetes; however, its mechanism is not fully understood. Evidence has recently revealed that long non-coding RNAs (lncRNAs) are abnormally expressed in DR, and lncRNAs may function as pivotal regulators. LncRNAs are able to modulate gene expression at the epigenetic level by acting as scaffolds of histone modification complexes and sponges of binding with microRNAs (miRNAs). LncRNAs are believed to be important epigenetic regulators, which may become beneficial in the diagnosis and therapy of DR. However, the mechanisms of lncRNAs in DR are still unclear. In this review, we summarize the possible functions and mechanisms of lncRNAs in epigenetic regulation to target genes in the progression of DR. Bentham Science Publishers 2022-08-11 2022-08-11 /pmc/articles/PMC9875540/ /pubmed/36777876 http://dx.doi.org/10.2174/1389202923666220531105035 Text en © 2022 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Genetics & Genomics
Song, Zhaoxia
He, Chang
Wen, Jianping
Yang, Jianli
Chen, Peng
Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy
title Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy
title_full Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy
title_fullStr Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy
title_full_unstemmed Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy
title_short Long Non-coding RNAs: Pivotal Epigenetic Regulators in Diabetic Retinopathy
title_sort long non-coding rnas: pivotal epigenetic regulators in diabetic retinopathy
topic Genetics & Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875540/
https://www.ncbi.nlm.nih.gov/pubmed/36777876
http://dx.doi.org/10.2174/1389202923666220531105035
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