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MALAT1 Long Non-Coding RNA: Functional Implications
The mammalian genome is pervasively transcribed and the functional significance of many long non-coding RNA (lncRNA) transcripts are gradually being elucidated. Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) is one of the most well-studied lncRNAs. MALAT1 is a highly conserved nucle...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344863/ https://www.ncbi.nlm.nih.gov/pubmed/32503170 http://dx.doi.org/10.3390/ncrna6020022 |
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author | Arun, Gayatri Aggarwal, Disha Spector, David L. |
author_facet | Arun, Gayatri Aggarwal, Disha Spector, David L. |
author_sort | Arun, Gayatri |
collection | PubMed |
description | The mammalian genome is pervasively transcribed and the functional significance of many long non-coding RNA (lncRNA) transcripts are gradually being elucidated. Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) is one of the most well-studied lncRNAs. MALAT1 is a highly conserved nuclear retained lncRNA that is abundantly expressed in cells and tissues and has been shown to play a role in regulating genes at both the transcriptional and post-transcriptional levels in a context-dependent manner. However, Malat1 has been shown to be dispensable for normal development and viability in mice. Interestingly, accumulating evidence suggests that MALAT1 plays an important role in numerous diseases including cancer. Here, we discuss the current state-of-knowledge in regard to MALAT1 with respect to its function, role in diseases, and the potential therapeutic opportunities for targeting MALAT1 using antisense oligonucleotides and small molecules. |
format | Online Article Text |
id | pubmed-7344863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73448632020-07-09 MALAT1 Long Non-Coding RNA: Functional Implications Arun, Gayatri Aggarwal, Disha Spector, David L. Noncoding RNA Review The mammalian genome is pervasively transcribed and the functional significance of many long non-coding RNA (lncRNA) transcripts are gradually being elucidated. Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) is one of the most well-studied lncRNAs. MALAT1 is a highly conserved nuclear retained lncRNA that is abundantly expressed in cells and tissues and has been shown to play a role in regulating genes at both the transcriptional and post-transcriptional levels in a context-dependent manner. However, Malat1 has been shown to be dispensable for normal development and viability in mice. Interestingly, accumulating evidence suggests that MALAT1 plays an important role in numerous diseases including cancer. Here, we discuss the current state-of-knowledge in regard to MALAT1 with respect to its function, role in diseases, and the potential therapeutic opportunities for targeting MALAT1 using antisense oligonucleotides and small molecules. MDPI 2020-06-03 /pmc/articles/PMC7344863/ /pubmed/32503170 http://dx.doi.org/10.3390/ncrna6020022 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Arun, Gayatri Aggarwal, Disha Spector, David L. MALAT1 Long Non-Coding RNA: Functional Implications |
title | MALAT1 Long Non-Coding RNA: Functional Implications |
title_full | MALAT1 Long Non-Coding RNA: Functional Implications |
title_fullStr | MALAT1 Long Non-Coding RNA: Functional Implications |
title_full_unstemmed | MALAT1 Long Non-Coding RNA: Functional Implications |
title_short | MALAT1 Long Non-Coding RNA: Functional Implications |
title_sort | malat1 long non-coding rna: functional implications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344863/ https://www.ncbi.nlm.nih.gov/pubmed/32503170 http://dx.doi.org/10.3390/ncrna6020022 |
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