MiRNAs as Players in Rhabdomyosarcoma Development

Rhabdomyosarcoma (RMS), the most common soft tissue sarcoma of childhood and adolescence, is a rare but aggressive malignancy that originates from immature mesenchymal cells committed to skeletal muscle differentiation. Although RMS is, generally, responsive to the modern multimodal therapeutic appr...

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Main Authors: Patrizia Gasparini, Andrea Ferrari, Michela Casanova, Francesca Limido, Maura Massimino, Gabriella Sozzi, Orazio Fortunato
Format: Article
Language:English
Published: MDPI AG 2019-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/22/5818
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spelling doaj-c39d442c7b544a388fc59687e860cdf52020-11-25T01:18:31ZengMDPI AGInternational Journal of Molecular Sciences1422-00672019-11-012022581810.3390/ijms20225818ijms20225818MiRNAs as Players in Rhabdomyosarcoma DevelopmentPatrizia Gasparini0Andrea Ferrari1Michela Casanova2Francesca Limido3Maura Massimino4Gabriella Sozzi5Orazio Fortunato6Tumor Genomics Unit, Department of Research; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyPediatric Oncology Unit; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyPediatric Oncology Unit; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyPediatric Oncology Unit; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyPediatric Oncology Unit; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyTumor Genomics Unit, Department of Research; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyTumor Genomics Unit, Department of Research; Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian 1, 20133 Milan, ItalyRhabdomyosarcoma (RMS), the most common soft tissue sarcoma of childhood and adolescence, is a rare but aggressive malignancy that originates from immature mesenchymal cells committed to skeletal muscle differentiation. Although RMS is, generally, responsive to the modern multimodal therapeutic approaches, the prognosis of RMS depends on multiple variables and for some patients the outcome remains dismal. Further comprehension of the molecular and cellular biology of RMS would lead to identification of novel therapeutic targets. MicroRNAs (miRNAs) are small non-coding RNAs proved to function as key regulators of skeletal muscle cell fate determination and to play important roles in RMS pathogenesis. The purpose of this review is to better delineate the role of miRNAs as a biomarkers or functional leaders in RMS development, so to possibly elucidate some of RMS molecular mechanisms and potentially therapeutically target them to improve clinical management of pediatric RMS.https://www.mdpi.com/1422-0067/20/22/5818rhabdomyosarcomamicrornapediatric tumors
collection DOAJ
language English
format Article
sources DOAJ
author Patrizia Gasparini
Andrea Ferrari
Michela Casanova
Francesca Limido
Maura Massimino
Gabriella Sozzi
Orazio Fortunato
spellingShingle Patrizia Gasparini
Andrea Ferrari
Michela Casanova
Francesca Limido
Maura Massimino
Gabriella Sozzi
Orazio Fortunato
MiRNAs as Players in Rhabdomyosarcoma Development
International Journal of Molecular Sciences
rhabdomyosarcoma
microrna
pediatric tumors
author_facet Patrizia Gasparini
Andrea Ferrari
Michela Casanova
Francesca Limido
Maura Massimino
Gabriella Sozzi
Orazio Fortunato
author_sort Patrizia Gasparini
title MiRNAs as Players in Rhabdomyosarcoma Development
title_short MiRNAs as Players in Rhabdomyosarcoma Development
title_full MiRNAs as Players in Rhabdomyosarcoma Development
title_fullStr MiRNAs as Players in Rhabdomyosarcoma Development
title_full_unstemmed MiRNAs as Players in Rhabdomyosarcoma Development
title_sort mirnas as players in rhabdomyosarcoma development
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2019-11-01
description Rhabdomyosarcoma (RMS), the most common soft tissue sarcoma of childhood and adolescence, is a rare but aggressive malignancy that originates from immature mesenchymal cells committed to skeletal muscle differentiation. Although RMS is, generally, responsive to the modern multimodal therapeutic approaches, the prognosis of RMS depends on multiple variables and for some patients the outcome remains dismal. Further comprehension of the molecular and cellular biology of RMS would lead to identification of novel therapeutic targets. MicroRNAs (miRNAs) are small non-coding RNAs proved to function as key regulators of skeletal muscle cell fate determination and to play important roles in RMS pathogenesis. The purpose of this review is to better delineate the role of miRNAs as a biomarkers or functional leaders in RMS development, so to possibly elucidate some of RMS molecular mechanisms and potentially therapeutically target them to improve clinical management of pediatric RMS.
topic rhabdomyosarcoma
microrna
pediatric tumors
url https://www.mdpi.com/1422-0067/20/22/5818
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