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Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions

Haematological malignancies encompass all variations of leukaemia at both the chronic and acute level, together with the specific cell type induced into tumourigenesis. Current diagnostic protocols for leukaemic conditions rely heavily on cytomorphology and other histological examinations from bone...

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Detalles Bibliográficos
Autores principales: Buhagiar, Alfred, Borg, Joseph, Ayers, Duncan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033436/
https://www.ncbi.nlm.nih.gov/pubmed/32110743
http://dx.doi.org/10.1016/j.ncrna.2020.02.001
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author Buhagiar, Alfred
Borg, Joseph
Ayers, Duncan
author_facet Buhagiar, Alfred
Borg, Joseph
Ayers, Duncan
author_sort Buhagiar, Alfred
collection PubMed
description Haematological malignancies encompass all variations of leukaemia at both the chronic and acute level, together with the specific cell type induced into tumourigenesis. Current diagnostic protocols for leukaemic conditions rely heavily on cytomorphology and other histological examinations from bone marrow aspirates, with the latter being a highly invasive surgical procedure for the patient. The discovery of microRNAs as one of the key gene regulatory networks in the past two decades has enabled researchers to investigate the possibility of exploiting the identification of dysregulated expression profiles for specific microRNAs present in the leukaemic patient's bloodstream as novel liquid biopsy diagnostic tools. This review article serves to consolidate recent global research efforts aiming to achieve such scopes.
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spelling pubmed-70334362020-02-27 Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions Buhagiar, Alfred Borg, Joseph Ayers, Duncan Noncoding RNA Res Article Haematological malignancies encompass all variations of leukaemia at both the chronic and acute level, together with the specific cell type induced into tumourigenesis. Current diagnostic protocols for leukaemic conditions rely heavily on cytomorphology and other histological examinations from bone marrow aspirates, with the latter being a highly invasive surgical procedure for the patient. The discovery of microRNAs as one of the key gene regulatory networks in the past two decades has enabled researchers to investigate the possibility of exploiting the identification of dysregulated expression profiles for specific microRNAs present in the leukaemic patient's bloodstream as novel liquid biopsy diagnostic tools. This review article serves to consolidate recent global research efforts aiming to achieve such scopes. KeAi Publishing 2020-02-19 /pmc/articles/PMC7033436/ /pubmed/32110743 http://dx.doi.org/10.1016/j.ncrna.2020.02.001 Text en © 2020 Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Buhagiar, Alfred
Borg, Joseph
Ayers, Duncan
Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions
title Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions
title_full Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions
title_fullStr Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions
title_full_unstemmed Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions
title_short Overview of current microRNA biomarker signatures as potential diagnostic tools for leukaemic conditions
title_sort overview of current microrna biomarker signatures as potential diagnostic tools for leukaemic conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033436/
https://www.ncbi.nlm.nih.gov/pubmed/32110743
http://dx.doi.org/10.1016/j.ncrna.2020.02.001
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