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CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out

Juvenile myelomonocytic leukemia (JMML), a rare myelodysplastic/myeloproliferative neoplasm of early childhood, is characterized by clonal growth of RAS signaling addicted stem cells. JMML subtypes are defined by specific RAS pathway mutations and display distinct gene, microRNA (miRNA) and long non...

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Autores principales: Dal Molin, Anna, Hofmans, Mattias, Gaffo, Enrico, Buratin, Alessia, Cavé, Hélène, Flotho, Christian, de Haas, Valerie, Niemeyer, Charlotte M., Stary, Jan, Van Vlierberghe, Pieter, Philippé, Jan, De Moerloose, Barbara, te Kronnie, Geertruij, Bresolin, Silvia, Lammens, Tim, Bortoluzzi, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815690/
https://www.ncbi.nlm.nih.gov/pubmed/33490078
http://dx.doi.org/10.3389/fcell.2020.613540
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author Dal Molin, Anna
Hofmans, Mattias
Gaffo, Enrico
Buratin, Alessia
Cavé, Hélène
Flotho, Christian
de Haas, Valerie
Niemeyer, Charlotte M.
Stary, Jan
Van Vlierberghe, Pieter
Philippé, Jan
De Moerloose, Barbara
te Kronnie, Geertruij
Bresolin, Silvia
Lammens, Tim
Bortoluzzi, Stefania
author_facet Dal Molin, Anna
Hofmans, Mattias
Gaffo, Enrico
Buratin, Alessia
Cavé, Hélène
Flotho, Christian
de Haas, Valerie
Niemeyer, Charlotte M.
Stary, Jan
Van Vlierberghe, Pieter
Philippé, Jan
De Moerloose, Barbara
te Kronnie, Geertruij
Bresolin, Silvia
Lammens, Tim
Bortoluzzi, Stefania
author_sort Dal Molin, Anna
collection PubMed
description Juvenile myelomonocytic leukemia (JMML), a rare myelodysplastic/myeloproliferative neoplasm of early childhood, is characterized by clonal growth of RAS signaling addicted stem cells. JMML subtypes are defined by specific RAS pathway mutations and display distinct gene, microRNA (miRNA) and long non-coding RNA expression profiles. Here we zoom in on circular RNAs (circRNAs), molecules that, when abnormally expressed, may participate in malignant deviation of cellular processes. CirComPara software was used to annotate and quantify circRNAs in RNA-seq data of a “discovery cohort” comprising 19 JMML patients and 3 healthy donors (HD). In an independent set of 12 JMML patients and 6 HD, expression of 27 circRNAs was analyzed by qRT-PCR. CircRNA-miRNA-gene networks were reconstructed using circRNA function prediction and gene expression data. We identified 119 circRNAs dysregulated in JMML and 59 genes showing an imbalance of the circular and linear products. Our data indicated also circRNA expression differences among molecular subgroups of JMML. Validation of a set of deregulated circRNAs in an independent cohort of JMML patients confirmed the down-regulation of circOXNAD1 and circATM, and a marked up-regulation of circLYN, circAFF2, and circMCTP1. A new finding in JMML links up-regulated circMCTP1 with known tumor suppressor miRNAs. This and other predicted interactions with miRNAs connect dysregulated circRNAs to regulatory networks. In conclusion, this study provides insight into the circRNAome of JMML and paves the path to elucidate new molecular disease mechanisms putting forward circMCTP1 up-regulation as a robust example.
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spelling pubmed-78156902021-01-21 CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out Dal Molin, Anna Hofmans, Mattias Gaffo, Enrico Buratin, Alessia Cavé, Hélène Flotho, Christian de Haas, Valerie Niemeyer, Charlotte M. Stary, Jan Van Vlierberghe, Pieter Philippé, Jan De Moerloose, Barbara te Kronnie, Geertruij Bresolin, Silvia Lammens, Tim Bortoluzzi, Stefania Front Cell Dev Biol Cell and Developmental Biology Juvenile myelomonocytic leukemia (JMML), a rare myelodysplastic/myeloproliferative neoplasm of early childhood, is characterized by clonal growth of RAS signaling addicted stem cells. JMML subtypes are defined by specific RAS pathway mutations and display distinct gene, microRNA (miRNA) and long non-coding RNA expression profiles. Here we zoom in on circular RNAs (circRNAs), molecules that, when abnormally expressed, may participate in malignant deviation of cellular processes. CirComPara software was used to annotate and quantify circRNAs in RNA-seq data of a “discovery cohort” comprising 19 JMML patients and 3 healthy donors (HD). In an independent set of 12 JMML patients and 6 HD, expression of 27 circRNAs was analyzed by qRT-PCR. CircRNA-miRNA-gene networks were reconstructed using circRNA function prediction and gene expression data. We identified 119 circRNAs dysregulated in JMML and 59 genes showing an imbalance of the circular and linear products. Our data indicated also circRNA expression differences among molecular subgroups of JMML. Validation of a set of deregulated circRNAs in an independent cohort of JMML patients confirmed the down-regulation of circOXNAD1 and circATM, and a marked up-regulation of circLYN, circAFF2, and circMCTP1. A new finding in JMML links up-regulated circMCTP1 with known tumor suppressor miRNAs. This and other predicted interactions with miRNAs connect dysregulated circRNAs to regulatory networks. In conclusion, this study provides insight into the circRNAome of JMML and paves the path to elucidate new molecular disease mechanisms putting forward circMCTP1 up-regulation as a robust example. Frontiers Media S.A. 2021-01-06 /pmc/articles/PMC7815690/ /pubmed/33490078 http://dx.doi.org/10.3389/fcell.2020.613540 Text en Copyright © 2021 Dal Molin, Hofmans, Gaffo, Buratin, Cavé, Flotho, de Haas, Niemeyer, Stary, Van Vlierberghe, Philippé, De Moerloose, te Kronnie, Bresolin, Lammens and Bortoluzzi. 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 Cell and Developmental Biology
Dal Molin, Anna
Hofmans, Mattias
Gaffo, Enrico
Buratin, Alessia
Cavé, Hélène
Flotho, Christian
de Haas, Valerie
Niemeyer, Charlotte M.
Stary, Jan
Van Vlierberghe, Pieter
Philippé, Jan
De Moerloose, Barbara
te Kronnie, Geertruij
Bresolin, Silvia
Lammens, Tim
Bortoluzzi, Stefania
CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out
title CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out
title_full CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out
title_fullStr CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out
title_full_unstemmed CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out
title_short CircRNAs Dysregulated in Juvenile Myelomonocytic Leukemia: CircMCTP1 Stands Out
title_sort circrnas dysregulated in juvenile myelomonocytic leukemia: circmctp1 stands out
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815690/
https://www.ncbi.nlm.nih.gov/pubmed/33490078
http://dx.doi.org/10.3389/fcell.2020.613540
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