Bone Deposition, Bone Resorption, and Osteosarcoma

Detalhes bibliográficos
Autor(a) principal: Toledo, Silvia Regina Caminada de [UNIFESP]
Data de Publicação: 2010
Outros Autores: Oliveira, Indhira Dias [UNIFESP], Okamoto, Oswaldo Keith [UNIFESP], Zago, Marco Antonio, Alves, Maria Teresa de Seixas [UNIFESP], Garcia Filho, Reynaldo Jesus [UNIFESP], Macedo, Carla Renata Donato Pacheco [UNIFESP], Petrilli, Antonio Sergio [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1002/jor.21120
http://repositorio.unifesp.br/handle/11600/32831
Resumo: Bone deposition and bone resorption are ongoing dynamic processes, constituting bone remodeling. Some bone tumors, such as osteosarcoma (OS), stimulate focal bone deposition. OS is the most common primary bone tumor in children and young adults. A complex network of genes regulates bone remodeling and alterations in its expression levels can influence the genesis and progression of bone diseases, including OS. We hypothesized that the expression profiles of bone remodeling regulator genes would be correlated with OS biology and clinical features. We used real-time PCR to evaluate the mRNA levels of the tartrate-resistant acid phosphatase (ACP5), colony stimulating factor-1 (CSF1R), bone morphogenetic protein 7 (BMP7), collagen, type XI, alpha 2 (COL11A2), and protein tyrosine phosphatases zeta 1 (PTPRZ1) genes, in 30 OS tumor samples and correlated with clinical and histological data. All genes analyzed, except CSF1R, were differentially expressed when compared with normal bone expression profiles. in our results, OS patients with high levels of COL11A2 mRNA showed worse overall (p = 0.041) and event free survival (p = 0.037). Also, a trend for better overall survival was observed in patients with samples showing higher expression of BMP7 (p =0.067). COL11A2 overexpression and BMP7 underexpression could collaborate to OS tumor growth, through its central role in bone remodeling process. (C) 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 28:1142-1148, 2010
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spelling Bone Deposition, Bone Resorption, and Osteosarcomaosteosarcomabone remodelingBMP7COL11A2Bone deposition and bone resorption are ongoing dynamic processes, constituting bone remodeling. Some bone tumors, such as osteosarcoma (OS), stimulate focal bone deposition. OS is the most common primary bone tumor in children and young adults. A complex network of genes regulates bone remodeling and alterations in its expression levels can influence the genesis and progression of bone diseases, including OS. We hypothesized that the expression profiles of bone remodeling regulator genes would be correlated with OS biology and clinical features. We used real-time PCR to evaluate the mRNA levels of the tartrate-resistant acid phosphatase (ACP5), colony stimulating factor-1 (CSF1R), bone morphogenetic protein 7 (BMP7), collagen, type XI, alpha 2 (COL11A2), and protein tyrosine phosphatases zeta 1 (PTPRZ1) genes, in 30 OS tumor samples and correlated with clinical and histological data. All genes analyzed, except CSF1R, were differentially expressed when compared with normal bone expression profiles. in our results, OS patients with high levels of COL11A2 mRNA showed worse overall (p = 0.041) and event free survival (p = 0.037). Also, a trend for better overall survival was observed in patients with samples showing higher expression of BMP7 (p =0.067). COL11A2 overexpression and BMP7 underexpression could collaborate to OS tumor growth, through its central role in bone remodeling process. (C) 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 28:1142-1148, 2010Universidade Federal de São Paulo, Dept Pediat, Pediat Oncol Grp, GRAACC,Genet Lab, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol & Genet, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Neurol & Neurosurg, BR-04023062 São Paulo, BrazilUniv São Paulo, Fac Med Ribeirao Preto, Ctr Cell Based Therapy, Ribeirao Preto, SP, BrazilUniversidade Federal de São Paulo, Dept Pathol, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Orthoped Surg & Traumatol, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pediat, Pediat Oncol Grp, GRAACC,Genet Lab, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morphol & Genet, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Neurol & Neurosurg, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pathol, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Orthoped Surg & Traumatol, BR-04023062 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)GRAACC (Grupo de Apoio ao Adolescente e Crianca corn Cancer)FAPESP: 04/12150-8FAPESP: 07/53869-3Wiley-BlackwellUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Toledo, Silvia Regina Caminada de [UNIFESP]Oliveira, Indhira Dias [UNIFESP]Okamoto, Oswaldo Keith [UNIFESP]Zago, Marco AntonioAlves, Maria Teresa de Seixas [UNIFESP]Garcia Filho, Reynaldo Jesus [UNIFESP]Macedo, Carla Renata Donato Pacheco [UNIFESP]Petrilli, Antonio Sergio [UNIFESP]2016-01-24T14:05:20Z2016-01-24T14:05:20Z2010-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1142-1148http://dx.doi.org/10.1002/jor.21120Journal of Orthopaedic Research. Hoboken: John Wiley & Sons Inc, v. 28, n. 9, p. 1142-1148, 2010.10.1002/jor.211200736-0266http://repositorio.unifesp.br/handle/11600/32831WOS:000280897100005engJournal of Orthopaedic Researchinfo:eu-repo/semantics/openAccesshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T12:05:20Zoai:repositorio.unifesp.br/:11600/32831Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T12:05:20Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Bone Deposition, Bone Resorption, and Osteosarcoma
title Bone Deposition, Bone Resorption, and Osteosarcoma
spellingShingle Bone Deposition, Bone Resorption, and Osteosarcoma
Toledo, Silvia Regina Caminada de [UNIFESP]
osteosarcoma
bone remodeling
BMP7
COL11A2
title_short Bone Deposition, Bone Resorption, and Osteosarcoma
title_full Bone Deposition, Bone Resorption, and Osteosarcoma
title_fullStr Bone Deposition, Bone Resorption, and Osteosarcoma
title_full_unstemmed Bone Deposition, Bone Resorption, and Osteosarcoma
title_sort Bone Deposition, Bone Resorption, and Osteosarcoma
author Toledo, Silvia Regina Caminada de [UNIFESP]
author_facet Toledo, Silvia Regina Caminada de [UNIFESP]
Oliveira, Indhira Dias [UNIFESP]
Okamoto, Oswaldo Keith [UNIFESP]
Zago, Marco Antonio
Alves, Maria Teresa de Seixas [UNIFESP]
Garcia Filho, Reynaldo Jesus [UNIFESP]
Macedo, Carla Renata Donato Pacheco [UNIFESP]
Petrilli, Antonio Sergio [UNIFESP]
author_role author
author2 Oliveira, Indhira Dias [UNIFESP]
Okamoto, Oswaldo Keith [UNIFESP]
Zago, Marco Antonio
Alves, Maria Teresa de Seixas [UNIFESP]
Garcia Filho, Reynaldo Jesus [UNIFESP]
Macedo, Carla Renata Donato Pacheco [UNIFESP]
Petrilli, Antonio Sergio [UNIFESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Toledo, Silvia Regina Caminada de [UNIFESP]
Oliveira, Indhira Dias [UNIFESP]
Okamoto, Oswaldo Keith [UNIFESP]
Zago, Marco Antonio
Alves, Maria Teresa de Seixas [UNIFESP]
Garcia Filho, Reynaldo Jesus [UNIFESP]
Macedo, Carla Renata Donato Pacheco [UNIFESP]
Petrilli, Antonio Sergio [UNIFESP]
dc.subject.por.fl_str_mv osteosarcoma
bone remodeling
BMP7
COL11A2
topic osteosarcoma
bone remodeling
BMP7
COL11A2
description Bone deposition and bone resorption are ongoing dynamic processes, constituting bone remodeling. Some bone tumors, such as osteosarcoma (OS), stimulate focal bone deposition. OS is the most common primary bone tumor in children and young adults. A complex network of genes regulates bone remodeling and alterations in its expression levels can influence the genesis and progression of bone diseases, including OS. We hypothesized that the expression profiles of bone remodeling regulator genes would be correlated with OS biology and clinical features. We used real-time PCR to evaluate the mRNA levels of the tartrate-resistant acid phosphatase (ACP5), colony stimulating factor-1 (CSF1R), bone morphogenetic protein 7 (BMP7), collagen, type XI, alpha 2 (COL11A2), and protein tyrosine phosphatases zeta 1 (PTPRZ1) genes, in 30 OS tumor samples and correlated with clinical and histological data. All genes analyzed, except CSF1R, were differentially expressed when compared with normal bone expression profiles. in our results, OS patients with high levels of COL11A2 mRNA showed worse overall (p = 0.041) and event free survival (p = 0.037). Also, a trend for better overall survival was observed in patients with samples showing higher expression of BMP7 (p =0.067). COL11A2 overexpression and BMP7 underexpression could collaborate to OS tumor growth, through its central role in bone remodeling process. (C) 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 28:1142-1148, 2010
publishDate 2010
dc.date.none.fl_str_mv 2010-09-01
2016-01-24T14:05:20Z
2016-01-24T14:05:20Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1002/jor.21120
Journal of Orthopaedic Research. Hoboken: John Wiley & Sons Inc, v. 28, n. 9, p. 1142-1148, 2010.
10.1002/jor.21120
0736-0266
http://repositorio.unifesp.br/handle/11600/32831
WOS:000280897100005
url http://dx.doi.org/10.1002/jor.21120
http://repositorio.unifesp.br/handle/11600/32831
identifier_str_mv Journal of Orthopaedic Research. Hoboken: John Wiley & Sons Inc, v. 28, n. 9, p. 1142-1148, 2010.
10.1002/jor.21120
0736-0266
WOS:000280897100005
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Orthopaedic Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.format.none.fl_str_mv 1142-1148
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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