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MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies

Myeloid malignancies, including myelodysplastic syndromes and acute myeloid leukemia, are clonal diseases arising in hematopoietic stem or progenitor cells. In recent years, microRNA (miRNA) expression profiling studies have revealed close associations of miRNAs with cytogenetic and molecular subtyp...

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Autores principales: Setijono, Stephanie Rebecca, Kwon, Hyog Young, Song, Su Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797589/
https://www.ncbi.nlm.nih.gov/pubmed/29441324
http://dx.doi.org/10.3389/fonc.2017.00331
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author Setijono, Stephanie Rebecca
Kwon, Hyog Young
Song, Su Jung
author_facet Setijono, Stephanie Rebecca
Kwon, Hyog Young
Song, Su Jung
author_sort Setijono, Stephanie Rebecca
collection PubMed
description Myeloid malignancies, including myelodysplastic syndromes and acute myeloid leukemia, are clonal diseases arising in hematopoietic stem or progenitor cells. In recent years, microRNA (miRNA) expression profiling studies have revealed close associations of miRNAs with cytogenetic and molecular subtypes of myeloid malignancies, as well as outcome and prognosis of patients. However, the roles of miRNA deregulation in the pathogenesis of myeloid malignancies and how they cooperate with protein-coding gene variants in pathological mechanisms leading to the diseases have not yet been fully understood. In this review, we focus on recent insights into the role of miRNAs in the development and progression of myeloid malignant diseases and discuss the prospect that miRNAs may serve as a potential therapeutic target for leukemia.
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spelling pubmed-57975892018-02-13 MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies Setijono, Stephanie Rebecca Kwon, Hyog Young Song, Su Jung Front Oncol Oncology Myeloid malignancies, including myelodysplastic syndromes and acute myeloid leukemia, are clonal diseases arising in hematopoietic stem or progenitor cells. In recent years, microRNA (miRNA) expression profiling studies have revealed close associations of miRNAs with cytogenetic and molecular subtypes of myeloid malignancies, as well as outcome and prognosis of patients. However, the roles of miRNA deregulation in the pathogenesis of myeloid malignancies and how they cooperate with protein-coding gene variants in pathological mechanisms leading to the diseases have not yet been fully understood. In this review, we focus on recent insights into the role of miRNAs in the development and progression of myeloid malignant diseases and discuss the prospect that miRNAs may serve as a potential therapeutic target for leukemia. Frontiers Media S.A. 2018-01-30 /pmc/articles/PMC5797589/ /pubmed/29441324 http://dx.doi.org/10.3389/fonc.2017.00331 Text en Copyright © 2018 Setijono, Kwon and Song. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Setijono, Stephanie Rebecca
Kwon, Hyog Young
Song, Su Jung
MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies
title MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies
title_full MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies
title_fullStr MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies
title_full_unstemmed MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies
title_short MicroRNA, an Antisense RNA, in Sensing Myeloid Malignancies
title_sort microrna, an antisense rna, in sensing myeloid malignancies
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797589/
https://www.ncbi.nlm.nih.gov/pubmed/29441324
http://dx.doi.org/10.3389/fonc.2017.00331
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