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Long noncoding RNAs: pivotal regulators in acute myeloid leukemia

Long noncoding RNAs (lncRNAs) have emerged as a class of pivotal regulators of gene expression. Recent studies have shown that lncRNAs contribute to the initiation, maintenance, and development of acute myeloid leukemia (AML). In this review, we summarize the current knowledge of the lncRNAs that pl...

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Detalles Bibliográficos
Autores principales: Wei, Shuyong, Wang, Kankan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153810/
https://www.ncbi.nlm.nih.gov/pubmed/27999732
http://dx.doi.org/10.1186/s40164-016-0059-9
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author Wei, Shuyong
Wang, Kankan
author_facet Wei, Shuyong
Wang, Kankan
author_sort Wei, Shuyong
collection PubMed
description Long noncoding RNAs (lncRNAs) have emerged as a class of pivotal regulators of gene expression. Recent studies have shown that lncRNAs contribute to the initiation, maintenance, and development of acute myeloid leukemia (AML). In this review, we summarize the current knowledge of the lncRNAs that play critical roles in AML. We first briefly describe the characteristics of lncRNAs, and then focus on their regulatory roles in AML, including the modulation of differentiation, proliferation, cell cycle, and apoptosis. We further emphasize the action of lncRNAs during leukemogenesis by describing how they interact with RNA, protein and chromatin DNA to exert their functions. We also highlight an urgent need to investigate the mechanisms by which lncRNAs contribute to the pathogenesis of AML. Finally, we discuss the prognostic value of lncRNAs in AML patients.
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spelling pubmed-51538102016-12-20 Long noncoding RNAs: pivotal regulators in acute myeloid leukemia Wei, Shuyong Wang, Kankan Exp Hematol Oncol Review Long noncoding RNAs (lncRNAs) have emerged as a class of pivotal regulators of gene expression. Recent studies have shown that lncRNAs contribute to the initiation, maintenance, and development of acute myeloid leukemia (AML). In this review, we summarize the current knowledge of the lncRNAs that play critical roles in AML. We first briefly describe the characteristics of lncRNAs, and then focus on their regulatory roles in AML, including the modulation of differentiation, proliferation, cell cycle, and apoptosis. We further emphasize the action of lncRNAs during leukemogenesis by describing how they interact with RNA, protein and chromatin DNA to exert their functions. We also highlight an urgent need to investigate the mechanisms by which lncRNAs contribute to the pathogenesis of AML. Finally, we discuss the prognostic value of lncRNAs in AML patients. BioMed Central 2016-12-12 /pmc/articles/PMC5153810/ /pubmed/27999732 http://dx.doi.org/10.1186/s40164-016-0059-9 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Wei, Shuyong
Wang, Kankan
Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
title Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
title_full Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
title_fullStr Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
title_full_unstemmed Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
title_short Long noncoding RNAs: pivotal regulators in acute myeloid leukemia
title_sort long noncoding rnas: pivotal regulators in acute myeloid leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153810/
https://www.ncbi.nlm.nih.gov/pubmed/27999732
http://dx.doi.org/10.1186/s40164-016-0059-9
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