Bone Deposition, Bone Resorption, and Osteosarcoma
Autor(a) principal: | |
---|---|
Data de Publicação: | 2010 |
Outros Autores: | , , , , , , |
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 |
id |
UFSP_807becfaf4a5ec495f70fef4cbe214ab |
---|---|
oai_identifier_str |
oai:repositorio.unifesp.br/:11600/32831 |
network_acronym_str |
UFSP |
network_name_str |
Repositório Institucional da UNIFESP |
repository_id_str |
3465 |
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 |
_version_ |
1814268370665603072 |