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Identification of Differentially Expressed MicroRNAs in Osteosarcoma

A limited number of reports have investigated the role of microRNAs in osteosarcoma. In this study, we performed miRNA expression profiling of osteosarcoma cell lines, tumor samples, and normal human osteoblasts. Twenty-two differentially expressed microRNAs were identified using high throughput rea...

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Detalles Bibliográficos
Autores principales: Lulla, Rishi R., Costa, Fabricio F., Bischof, Jared M., Chou, Pauline M., Bonaldo, Maria de F., Vanin, Elio F., Soares, Marcelo B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140035/
https://www.ncbi.nlm.nih.gov/pubmed/21789031
http://dx.doi.org/10.1155/2011/732690
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author Lulla, Rishi R.
Costa, Fabricio F.
Bischof, Jared M.
Chou, Pauline M.
Bonaldo, Maria de F.
Vanin, Elio F.
Soares, Marcelo B.
author_facet Lulla, Rishi R.
Costa, Fabricio F.
Bischof, Jared M.
Chou, Pauline M.
Bonaldo, Maria de F.
Vanin, Elio F.
Soares, Marcelo B.
author_sort Lulla, Rishi R.
collection PubMed
description A limited number of reports have investigated the role of microRNAs in osteosarcoma. In this study, we performed miRNA expression profiling of osteosarcoma cell lines, tumor samples, and normal human osteoblasts. Twenty-two differentially expressed microRNAs were identified using high throughput real-time PCR analysis, and 4 (miR-135b, miR-150, miR-542-5p, and miR-652) were confirmed and validated in a different group of tumors. Both miR-135b and miR-150 have been previously shown to be important in cancer. We hypothesize that dysregulation of differentially expressed microRNAs may contribute to tumorigenesis. They might also represent molecular biomarkers or targets for drug development in osteosarcoma.
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spelling pubmed-31400352011-07-25 Identification of Differentially Expressed MicroRNAs in Osteosarcoma Lulla, Rishi R. Costa, Fabricio F. Bischof, Jared M. Chou, Pauline M. Bonaldo, Maria de F. Vanin, Elio F. Soares, Marcelo B. Sarcoma Research Article A limited number of reports have investigated the role of microRNAs in osteosarcoma. In this study, we performed miRNA expression profiling of osteosarcoma cell lines, tumor samples, and normal human osteoblasts. Twenty-two differentially expressed microRNAs were identified using high throughput real-time PCR analysis, and 4 (miR-135b, miR-150, miR-542-5p, and miR-652) were confirmed and validated in a different group of tumors. Both miR-135b and miR-150 have been previously shown to be important in cancer. We hypothesize that dysregulation of differentially expressed microRNAs may contribute to tumorigenesis. They might also represent molecular biomarkers or targets for drug development in osteosarcoma. Hindawi Publishing Corporation 2011 2011-07-18 /pmc/articles/PMC3140035/ /pubmed/21789031 http://dx.doi.org/10.1155/2011/732690 Text en Copyright © 2011 Rishi R. Lulla et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lulla, Rishi R.
Costa, Fabricio F.
Bischof, Jared M.
Chou, Pauline M.
Bonaldo, Maria de F.
Vanin, Elio F.
Soares, Marcelo B.
Identification of Differentially Expressed MicroRNAs in Osteosarcoma
title Identification of Differentially Expressed MicroRNAs in Osteosarcoma
title_full Identification of Differentially Expressed MicroRNAs in Osteosarcoma
title_fullStr Identification of Differentially Expressed MicroRNAs in Osteosarcoma
title_full_unstemmed Identification of Differentially Expressed MicroRNAs in Osteosarcoma
title_short Identification of Differentially Expressed MicroRNAs in Osteosarcoma
title_sort identification of differentially expressed micrornas in osteosarcoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140035/
https://www.ncbi.nlm.nih.gov/pubmed/21789031
http://dx.doi.org/10.1155/2011/732690
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