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Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone
Though benign, giant cell tumor of bone (GCTB) can become aggressive and can exhibit a high mitotic rate, necrosis and rarely vascular invasion and metastasis. GCTB has unique histologic characteristics, a high rate of multinucleated cells, a variable and unpredictable growth potential and uncertain...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Ivyspring International Publisher
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4466407/ https://www.ncbi.nlm.nih.gov/pubmed/26078788 http://dx.doi.org/10.7150/jca.11238 |
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author | Conceição, André Luis Giacometti Babeto, Erica Candido, Natalia Maria Franco, Fernanda Craveiro de Campos Zuccari, Débora Aparecida Pires Bonilha, Jane Lopes Cordeiro, José Antônio Calmon, Marilia Freitas Rahal, Paula |
author_facet | Conceição, André Luis Giacometti Babeto, Erica Candido, Natalia Maria Franco, Fernanda Craveiro de Campos Zuccari, Débora Aparecida Pires Bonilha, Jane Lopes Cordeiro, José Antônio Calmon, Marilia Freitas Rahal, Paula |
author_sort | Conceição, André Luis Giacometti |
collection | PubMed |
description | Though benign, giant cell tumor of bone (GCTB) can become aggressive and can exhibit a high mitotic rate, necrosis and rarely vascular invasion and metastasis. GCTB has unique histologic characteristics, a high rate of multinucleated cells, a variable and unpredictable growth potential and uncertain biological behavior. In this study, we sought to identify genes differentially expressed in GCTB, thus building a molecular profile of this tumor. We performed quantitative real-time polymerase chain reaction (qPCR), immunohistochemistry and analyses of methylation to identify genes that are putatively associated with GCTB. The expression of the ADAM23 and CDKN2A genes was decreased in GCTB samples compared to normal bone tissue, measured by qPCR. Additionally, a high hypermethylation frequency of the promoter regions of ADAM23 and CDKN2A in GCTB was observed. The expression of the MAP2K3, MMP14, TIMP2 and VIM genes was significantly higher in GCTB than in normal bone tissue, a fact that was confirmed by qPCR and immunohistochemistry. The set of genes identified here furthers our understanding of the molecular basis of GCTB. |
format | Online Article Text |
id | pubmed-4466407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-44664072015-06-15 Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone Conceição, André Luis Giacometti Babeto, Erica Candido, Natalia Maria Franco, Fernanda Craveiro de Campos Zuccari, Débora Aparecida Pires Bonilha, Jane Lopes Cordeiro, José Antônio Calmon, Marilia Freitas Rahal, Paula J Cancer Research Paper Though benign, giant cell tumor of bone (GCTB) can become aggressive and can exhibit a high mitotic rate, necrosis and rarely vascular invasion and metastasis. GCTB has unique histologic characteristics, a high rate of multinucleated cells, a variable and unpredictable growth potential and uncertain biological behavior. In this study, we sought to identify genes differentially expressed in GCTB, thus building a molecular profile of this tumor. We performed quantitative real-time polymerase chain reaction (qPCR), immunohistochemistry and analyses of methylation to identify genes that are putatively associated with GCTB. The expression of the ADAM23 and CDKN2A genes was decreased in GCTB samples compared to normal bone tissue, measured by qPCR. Additionally, a high hypermethylation frequency of the promoter regions of ADAM23 and CDKN2A in GCTB was observed. The expression of the MAP2K3, MMP14, TIMP2 and VIM genes was significantly higher in GCTB than in normal bone tissue, a fact that was confirmed by qPCR and immunohistochemistry. The set of genes identified here furthers our understanding of the molecular basis of GCTB. Ivyspring International Publisher 2015-05-23 /pmc/articles/PMC4466407/ /pubmed/26078788 http://dx.doi.org/10.7150/jca.11238 Text en © 2015 Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions. |
spellingShingle | Research Paper Conceição, André Luis Giacometti Babeto, Erica Candido, Natalia Maria Franco, Fernanda Craveiro de Campos Zuccari, Débora Aparecida Pires Bonilha, Jane Lopes Cordeiro, José Antônio Calmon, Marilia Freitas Rahal, Paula Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone |
title | Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone |
title_full | Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone |
title_fullStr | Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone |
title_full_unstemmed | Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone |
title_short | Differential Expression of ADAM23, CDKN2A (P16), MMP14 and VIM Associated with Giant Cell Tumor of Bone |
title_sort | differential expression of adam23, cdkn2a (p16), mmp14 and vim associated with giant cell tumor of bone |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4466407/ https://www.ncbi.nlm.nih.gov/pubmed/26078788 http://dx.doi.org/10.7150/jca.11238 |
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