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Circular RNAs in Blood Malignancies

Circular (circ)RNAs influence a wide range of biological processes at least in part by interacting with proteins and microRNAs. CircRNAs expressed in the hematopoietic compartment have been increasingly recognized as modulators of physiological and pathological features of hematopoetic stem cell (HS...

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Autores principales: Perez de Acha, Olivia, Rossi, Martina, Gorospe, Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333357/
https://www.ncbi.nlm.nih.gov/pubmed/32676504
http://dx.doi.org/10.3389/fmolb.2020.00109
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author Perez de Acha, Olivia
Rossi, Martina
Gorospe, Myriam
author_facet Perez de Acha, Olivia
Rossi, Martina
Gorospe, Myriam
author_sort Perez de Acha, Olivia
collection PubMed
description Circular (circ)RNAs influence a wide range of biological processes at least in part by interacting with proteins and microRNAs. CircRNAs expressed in the hematopoietic compartment have been increasingly recognized as modulators of physiological and pathological features of hematopoetic stem cell (HSC)-derived populations. In particular, several circRNAs were found to enhance or suppress tumor progression in blood malignancies such as leukemias and lymphomas. Moreover, numerous circRNAs have been proposed to help confer resistance to the conventional treatments used in hematopoietic cancers. Here, we review the most important circRNAs described thus far in acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), lymphomas, and multiple myeloma (MM). We discuss the usefulness of circRNAs as diagnostic and prognostic markers and their potential value as therapeutic targets.
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spelling pubmed-73333572020-07-15 Circular RNAs in Blood Malignancies Perez de Acha, Olivia Rossi, Martina Gorospe, Myriam Front Mol Biosci Molecular Biosciences Circular (circ)RNAs influence a wide range of biological processes at least in part by interacting with proteins and microRNAs. CircRNAs expressed in the hematopoietic compartment have been increasingly recognized as modulators of physiological and pathological features of hematopoetic stem cell (HSC)-derived populations. In particular, several circRNAs were found to enhance or suppress tumor progression in blood malignancies such as leukemias and lymphomas. Moreover, numerous circRNAs have been proposed to help confer resistance to the conventional treatments used in hematopoietic cancers. Here, we review the most important circRNAs described thus far in acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL), lymphomas, and multiple myeloma (MM). We discuss the usefulness of circRNAs as diagnostic and prognostic markers and their potential value as therapeutic targets. Frontiers Media S.A. 2020-06-26 /pmc/articles/PMC7333357/ /pubmed/32676504 http://dx.doi.org/10.3389/fmolb.2020.00109 Text en Copyright © 2020 Perez de Acha, Rossi and Gorospe. 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(s) 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 Molecular Biosciences
Perez de Acha, Olivia
Rossi, Martina
Gorospe, Myriam
Circular RNAs in Blood Malignancies
title Circular RNAs in Blood Malignancies
title_full Circular RNAs in Blood Malignancies
title_fullStr Circular RNAs in Blood Malignancies
title_full_unstemmed Circular RNAs in Blood Malignancies
title_short Circular RNAs in Blood Malignancies
title_sort circular rnas in blood malignancies
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333357/
https://www.ncbi.nlm.nih.gov/pubmed/32676504
http://dx.doi.org/10.3389/fmolb.2020.00109
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