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MicroRNA expression and activity in T-cell acute lymphoblastic leukemia

T-cell acute lymphoblastic leukemia (T-ALL) is a lymphoid malignancy caused by the oncogenic transformation of immature T-cell progenitors. Many biologically relevant genetic and epigenetic alterations have been identified as driving factors for this transformation. Recently, microRNAs (miRNAs) have...

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Detalles Bibliográficos
Autor principal: Ye, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797063/
https://www.ncbi.nlm.nih.gov/pubmed/29435192
http://dx.doi.org/10.18632/oncotarget.23539
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author Ye, Fang
author_facet Ye, Fang
author_sort Ye, Fang
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description T-cell acute lymphoblastic leukemia (T-ALL) is a lymphoid malignancy caused by the oncogenic transformation of immature T-cell progenitors. Many biologically relevant genetic and epigenetic alterations have been identified as driving factors for this transformation. Recently, microRNAs (miRNAs) have been shown to influence various leukemias, including T-ALL. Aberrant expression of miRNAs can function as either oncogenes or tumor suppressors in T-ALL through the regulation of cell migration, invasion, proliferation, apoptosis, and chemoresistance. This occurs by targeting key signaling pathways or transcriptional factors that play a critical role in T-ALL pathology and progression. Different miRNA expression profiles have been linked to specific genetic subtypes of human T-ALL. Furthermore, miRNAs can also act as independent prognostic factors to predict clinical outcomes for T-ALL patients. In the current review, we will focus on the role of miRNAs in the development and progression of T-ALL.
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spelling pubmed-57970632018-02-12 MicroRNA expression and activity in T-cell acute lymphoblastic leukemia Ye, Fang Oncotarget Review T-cell acute lymphoblastic leukemia (T-ALL) is a lymphoid malignancy caused by the oncogenic transformation of immature T-cell progenitors. Many biologically relevant genetic and epigenetic alterations have been identified as driving factors for this transformation. Recently, microRNAs (miRNAs) have been shown to influence various leukemias, including T-ALL. Aberrant expression of miRNAs can function as either oncogenes or tumor suppressors in T-ALL through the regulation of cell migration, invasion, proliferation, apoptosis, and chemoresistance. This occurs by targeting key signaling pathways or transcriptional factors that play a critical role in T-ALL pathology and progression. Different miRNA expression profiles have been linked to specific genetic subtypes of human T-ALL. Furthermore, miRNAs can also act as independent prognostic factors to predict clinical outcomes for T-ALL patients. In the current review, we will focus on the role of miRNAs in the development and progression of T-ALL. Impact Journals LLC 2017-12-20 /pmc/articles/PMC5797063/ /pubmed/29435192 http://dx.doi.org/10.18632/oncotarget.23539 Text en Copyright: © 2018 Ye http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Review
Ye, Fang
MicroRNA expression and activity in T-cell acute lymphoblastic leukemia
title MicroRNA expression and activity in T-cell acute lymphoblastic leukemia
title_full MicroRNA expression and activity in T-cell acute lymphoblastic leukemia
title_fullStr MicroRNA expression and activity in T-cell acute lymphoblastic leukemia
title_full_unstemmed MicroRNA expression and activity in T-cell acute lymphoblastic leukemia
title_short MicroRNA expression and activity in T-cell acute lymphoblastic leukemia
title_sort microrna expression and activity in t-cell acute lymphoblastic leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797063/
https://www.ncbi.nlm.nih.gov/pubmed/29435192
http://dx.doi.org/10.18632/oncotarget.23539
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