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MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia

In the relatively short period of time since their discovery, microRNAs have been shown to control many important cellular functions such as cell differentiation, growth, proliferation and apoptosis. In addition, microRNAs have been demonstrated as key drivers of many malignancies and can function a...

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Detalles Bibliográficos
Autores principales: Palma, Catalina A, Tonna, Elise J, Ma, David F, Lutherborrow, Mark A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365878/
https://www.ncbi.nlm.nih.gov/pubmed/22225649
http://dx.doi.org/10.1111/j.1582-4934.2011.01514.x
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author Palma, Catalina A
Tonna, Elise J
Ma, David F
Lutherborrow, Mark A
author_facet Palma, Catalina A
Tonna, Elise J
Ma, David F
Lutherborrow, Mark A
author_sort Palma, Catalina A
collection PubMed
description In the relatively short period of time since their discovery, microRNAs have been shown to control many important cellular functions such as cell differentiation, growth, proliferation and apoptosis. In addition, microRNAs have been demonstrated as key drivers of many malignancies and can function as either tumour suppressors or oncogenes. The haematopoietic system is not outside the realm of microRNA control with microRNAs controlling aspects of stem cell and progenitor self-renewal and differentiation, with many, if not all, haematological disorders associated with aberrant microRNA expression and function. In this review, we focus on the current understanding of microRNA control of haematopoiesis and detail the evidence for the contribution and clinical relevance of aberrant microRNA function to the characteristic block of differentiation in acute myeloid leukaemia.
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spelling pubmed-43658782015-03-27 MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia Palma, Catalina A Tonna, Elise J Ma, David F Lutherborrow, Mark A J Cell Mol Med Reviews In the relatively short period of time since their discovery, microRNAs have been shown to control many important cellular functions such as cell differentiation, growth, proliferation and apoptosis. In addition, microRNAs have been demonstrated as key drivers of many malignancies and can function as either tumour suppressors or oncogenes. The haematopoietic system is not outside the realm of microRNA control with microRNAs controlling aspects of stem cell and progenitor self-renewal and differentiation, with many, if not all, haematological disorders associated with aberrant microRNA expression and function. In this review, we focus on the current understanding of microRNA control of haematopoiesis and detail the evidence for the contribution and clinical relevance of aberrant microRNA function to the characteristic block of differentiation in acute myeloid leukaemia. Blackwell Publishing Ltd 2012-05 2012-04-26 /pmc/articles/PMC4365878/ /pubmed/22225649 http://dx.doi.org/10.1111/j.1582-4934.2011.01514.x Text en Copyright © 2012 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.
spellingShingle Reviews
Palma, Catalina A
Tonna, Elise J
Ma, David F
Lutherborrow, Mark A
MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia
title MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia
title_full MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia
title_fullStr MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia
title_full_unstemmed MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia
title_short MicroRNA control of myelopoiesis and the differentiation block in acute myeloid leukaemia
title_sort microrna control of myelopoiesis and the differentiation block in acute myeloid leukaemia
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365878/
https://www.ncbi.nlm.nih.gov/pubmed/22225649
http://dx.doi.org/10.1111/j.1582-4934.2011.01514.x
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