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Involvement and Clinical Aspects of MicroRNA in Osteosarcoma

Osteosarcoma (OS) is the most common primary bone cancer in children and adolescents, but its pathogenesis has been difficult to establish because of its well-known heterogeneous nature. OS has been associated with genetic and cytogenetic abnormalities, which include function-impairing mutations in...

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Detalles Bibliográficos
Autores principales: Ram Kumar, Ram Mohan, Boro, Aleksandar, Fuchs, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926411/
https://www.ncbi.nlm.nih.gov/pubmed/27271607
http://dx.doi.org/10.3390/ijms17060877
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author Ram Kumar, Ram Mohan
Boro, Aleksandar
Fuchs, Bruno
author_facet Ram Kumar, Ram Mohan
Boro, Aleksandar
Fuchs, Bruno
author_sort Ram Kumar, Ram Mohan
collection PubMed
description Osteosarcoma (OS) is the most common primary bone cancer in children and adolescents, but its pathogenesis has been difficult to establish because of its well-known heterogeneous nature. OS has been associated with genetic and cytogenetic abnormalities, which include function-impairing mutations in tumor suppressors and the activation of oncogenes. OS tumorigenesis has been linked to alterations of several genes characterized by a high level of genetic instability and recurrent DNA amplifications and deletions. MicroRNAs (miRNAs), 18–25-nucleotide noncoding RNAs, are critical for various biological processes like differentiation, cell growth and cell death. Dysregulation of miRNA expression leads to phenotypic and genotypic changes in cells, which leads to cancer. Studies on miRNAs have initiated a significant effect in both diagnosis and treatment of cancer. This review focuses on the current knowledge of clinical applications of miRNAs for the better diagnosis and management of OS.
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spelling pubmed-49264112016-07-06 Involvement and Clinical Aspects of MicroRNA in Osteosarcoma Ram Kumar, Ram Mohan Boro, Aleksandar Fuchs, Bruno Int J Mol Sci Review Osteosarcoma (OS) is the most common primary bone cancer in children and adolescents, but its pathogenesis has been difficult to establish because of its well-known heterogeneous nature. OS has been associated with genetic and cytogenetic abnormalities, which include function-impairing mutations in tumor suppressors and the activation of oncogenes. OS tumorigenesis has been linked to alterations of several genes characterized by a high level of genetic instability and recurrent DNA amplifications and deletions. MicroRNAs (miRNAs), 18–25-nucleotide noncoding RNAs, are critical for various biological processes like differentiation, cell growth and cell death. Dysregulation of miRNA expression leads to phenotypic and genotypic changes in cells, which leads to cancer. Studies on miRNAs have initiated a significant effect in both diagnosis and treatment of cancer. This review focuses on the current knowledge of clinical applications of miRNAs for the better diagnosis and management of OS. MDPI 2016-06-03 /pmc/articles/PMC4926411/ /pubmed/27271607 http://dx.doi.org/10.3390/ijms17060877 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ram Kumar, Ram Mohan
Boro, Aleksandar
Fuchs, Bruno
Involvement and Clinical Aspects of MicroRNA in Osteosarcoma
title Involvement and Clinical Aspects of MicroRNA in Osteosarcoma
title_full Involvement and Clinical Aspects of MicroRNA in Osteosarcoma
title_fullStr Involvement and Clinical Aspects of MicroRNA in Osteosarcoma
title_full_unstemmed Involvement and Clinical Aspects of MicroRNA in Osteosarcoma
title_short Involvement and Clinical Aspects of MicroRNA in Osteosarcoma
title_sort involvement and clinical aspects of microrna in osteosarcoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926411/
https://www.ncbi.nlm.nih.gov/pubmed/27271607
http://dx.doi.org/10.3390/ijms17060877
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