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MicroRNA: Important Player in the Pathobiology of Multiple Myeloma

Recent studies have revealed a pivotal role played by a class of small, noncoding RNAs, microRNA (miRNA), in multiple myeloma (MM), a plasma cell (PC) malignancy causing significant morbidity and mortality. Deregulated miRNA expression in patient's PCs and plasma has been associated with tumor...

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Detalles Bibliográficos
Autores principales: Bi, Chonglei, Chng, Wee Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065722/
https://www.ncbi.nlm.nih.gov/pubmed/24991558
http://dx.doi.org/10.1155/2014/521586
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author Bi, Chonglei
Chng, Wee Joo
author_facet Bi, Chonglei
Chng, Wee Joo
author_sort Bi, Chonglei
collection PubMed
description Recent studies have revealed a pivotal role played by a class of small, noncoding RNAs, microRNA (miRNA), in multiple myeloma (MM), a plasma cell (PC) malignancy causing significant morbidity and mortality. Deregulated miRNA expression in patient's PCs and plasma has been associated with tumor progression, molecular subtypes, clinical staging, prognosis, and drug response in MM. A number of important oncogenic and tumor suppressor miRNAs have been discovered to regulate important genes and pathways such as p53 and IL6-JAK-STAT signaling. miRNAs may also form complex regulatory circuitry with genetic and epigenetic machineries, the deregulation of which could lead to malignant transformation and progression. The translational potential of miRNAs in the clinic is being increasingly recognized that they could represent novel biomarkers and therapeutic targets. This review comprehensively summarizes current progress in delineating the roles of miRNAs in MM pathobiology and management.
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spelling pubmed-40657222014-07-02 MicroRNA: Important Player in the Pathobiology of Multiple Myeloma Bi, Chonglei Chng, Wee Joo Biomed Res Int Review Article Recent studies have revealed a pivotal role played by a class of small, noncoding RNAs, microRNA (miRNA), in multiple myeloma (MM), a plasma cell (PC) malignancy causing significant morbidity and mortality. Deregulated miRNA expression in patient's PCs and plasma has been associated with tumor progression, molecular subtypes, clinical staging, prognosis, and drug response in MM. A number of important oncogenic and tumor suppressor miRNAs have been discovered to regulate important genes and pathways such as p53 and IL6-JAK-STAT signaling. miRNAs may also form complex regulatory circuitry with genetic and epigenetic machineries, the deregulation of which could lead to malignant transformation and progression. The translational potential of miRNAs in the clinic is being increasingly recognized that they could represent novel biomarkers and therapeutic targets. This review comprehensively summarizes current progress in delineating the roles of miRNAs in MM pathobiology and management. Hindawi Publishing Corporation 2014 2014-06-03 /pmc/articles/PMC4065722/ /pubmed/24991558 http://dx.doi.org/10.1155/2014/521586 Text en Copyright © 2014 C. Bi and W. J. Chng. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Bi, Chonglei
Chng, Wee Joo
MicroRNA: Important Player in the Pathobiology of Multiple Myeloma
title MicroRNA: Important Player in the Pathobiology of Multiple Myeloma
title_full MicroRNA: Important Player in the Pathobiology of Multiple Myeloma
title_fullStr MicroRNA: Important Player in the Pathobiology of Multiple Myeloma
title_full_unstemmed MicroRNA: Important Player in the Pathobiology of Multiple Myeloma
title_short MicroRNA: Important Player in the Pathobiology of Multiple Myeloma
title_sort microrna: important player in the pathobiology of multiple myeloma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065722/
https://www.ncbi.nlm.nih.gov/pubmed/24991558
http://dx.doi.org/10.1155/2014/521586
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