TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.

Detalhes bibliográficos
Autor(a) principal: Lima-Ramos, V
Data de Publicação: 2008
Outros Autores: Pacheco-Figueiredo, L, Costa, S, Pardal, F, Silva, A, Amorim, J, Lopes, JM, Reis, RM
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.23/451
Resumo: TP53 is a key tumor suppressor gene that encodes a transcriptional factor involved in several cellular mechanisms, including growth arrest, DNA repair, and induction of apoptosis. In addition to TP53 gene mutations, a common polymorphism, Arg72Pro, has been involved in the carcinogenesis process. The Pro72 variant has been associated with a slower induction of apoptosis and may influence the risk of cancer development. The role of Arg72Pro polymorphism in glioma susceptibility is poorly characterized. With the objective of analyzing the role of the TP53 Arg72Pro polymorphism in glioma risk, overall survival, and patient therapy response in a Portuguese population, we conducted a retrospective case-control study, including 171 patients with gliomas and 526 cancer-free individuals. The Arg72Pro genotype was assessed by the polymerase chain reaction-restriction fragment length polymorphism technique. No statistically significant differences were observed in the genotypic and allelic frequencies between glioma and control groups, and no statistically significant differences were observed with stratification of gliomas into distinct histological subtypes: astrocytic (n = 115), glioblastoma (n = 75), and oligodendroglial (n = 54) tumors. No significant association was observed between TP53 Arg72Pro and patient overall survival, but Kaplan-Meier analysis of glioma patients harboring the Pro72 allele showed a significantly longer survival with adjuvant therapy. In this first assessment of the role of TP53 Arg72Pro polymorphism in a large series of Portuguese glioma tumors, no association was observed with glioma susceptibility or overall survival, except for patients submitted to adjuvant therapy.
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spelling TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.Neoplasias CerebraisGliomaPredisposição Genética para DoençaPolimorfismo GenéticoGenes p53TP53 is a key tumor suppressor gene that encodes a transcriptional factor involved in several cellular mechanisms, including growth arrest, DNA repair, and induction of apoptosis. In addition to TP53 gene mutations, a common polymorphism, Arg72Pro, has been involved in the carcinogenesis process. The Pro72 variant has been associated with a slower induction of apoptosis and may influence the risk of cancer development. The role of Arg72Pro polymorphism in glioma susceptibility is poorly characterized. With the objective of analyzing the role of the TP53 Arg72Pro polymorphism in glioma risk, overall survival, and patient therapy response in a Portuguese population, we conducted a retrospective case-control study, including 171 patients with gliomas and 526 cancer-free individuals. The Arg72Pro genotype was assessed by the polymerase chain reaction-restriction fragment length polymorphism technique. No statistically significant differences were observed in the genotypic and allelic frequencies between glioma and control groups, and no statistically significant differences were observed with stratification of gliomas into distinct histological subtypes: astrocytic (n = 115), glioblastoma (n = 75), and oligodendroglial (n = 54) tumors. No significant association was observed between TP53 Arg72Pro and patient overall survival, but Kaplan-Meier analysis of glioma patients harboring the Pro72 allele showed a significantly longer survival with adjuvant therapy. In this first assessment of the role of TP53 Arg72Pro polymorphism in a large series of Portuguese glioma tumors, no association was observed with glioma susceptibility or overall survival, except for patients submitted to adjuvant therapy.Repositório Científico do Hospital de BragaLima-Ramos, VPacheco-Figueiredo, LCosta, SPardal, FSilva, AAmorim, JLopes, JMReis, RM2013-06-21T13:55:07Z2008-01-01T00:00:00Z2008-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.23/451engCancer Genet Cytogenet. 2008;180(1):14-9.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-21T09:02:05Zoai:repositorio.hospitaldebraga.pt:10400.23/451Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:54:58.781464Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
title TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
spellingShingle TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
Lima-Ramos, V
Neoplasias Cerebrais
Glioma
Predisposição Genética para Doença
Polimorfismo Genético
Genes p53
title_short TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
title_full TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
title_fullStr TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
title_full_unstemmed TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
title_sort TP53 codon 72 polymorphism in susceptibility, overall survival, and adjuvant therapy response of gliomas.
author Lima-Ramos, V
author_facet Lima-Ramos, V
Pacheco-Figueiredo, L
Costa, S
Pardal, F
Silva, A
Amorim, J
Lopes, JM
Reis, RM
author_role author
author2 Pacheco-Figueiredo, L
Costa, S
Pardal, F
Silva, A
Amorim, J
Lopes, JM
Reis, RM
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Hospital de Braga
dc.contributor.author.fl_str_mv Lima-Ramos, V
Pacheco-Figueiredo, L
Costa, S
Pardal, F
Silva, A
Amorim, J
Lopes, JM
Reis, RM
dc.subject.por.fl_str_mv Neoplasias Cerebrais
Glioma
Predisposição Genética para Doença
Polimorfismo Genético
Genes p53
topic Neoplasias Cerebrais
Glioma
Predisposição Genética para Doença
Polimorfismo Genético
Genes p53
description TP53 is a key tumor suppressor gene that encodes a transcriptional factor involved in several cellular mechanisms, including growth arrest, DNA repair, and induction of apoptosis. In addition to TP53 gene mutations, a common polymorphism, Arg72Pro, has been involved in the carcinogenesis process. The Pro72 variant has been associated with a slower induction of apoptosis and may influence the risk of cancer development. The role of Arg72Pro polymorphism in glioma susceptibility is poorly characterized. With the objective of analyzing the role of the TP53 Arg72Pro polymorphism in glioma risk, overall survival, and patient therapy response in a Portuguese population, we conducted a retrospective case-control study, including 171 patients with gliomas and 526 cancer-free individuals. The Arg72Pro genotype was assessed by the polymerase chain reaction-restriction fragment length polymorphism technique. No statistically significant differences were observed in the genotypic and allelic frequencies between glioma and control groups, and no statistically significant differences were observed with stratification of gliomas into distinct histological subtypes: astrocytic (n = 115), glioblastoma (n = 75), and oligodendroglial (n = 54) tumors. No significant association was observed between TP53 Arg72Pro and patient overall survival, but Kaplan-Meier analysis of glioma patients harboring the Pro72 allele showed a significantly longer survival with adjuvant therapy. In this first assessment of the role of TP53 Arg72Pro polymorphism in a large series of Portuguese glioma tumors, no association was observed with glioma susceptibility or overall survival, except for patients submitted to adjuvant therapy.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01T00:00:00Z
2008-01-01T00:00:00Z
2013-06-21T13:55:07Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.23/451
url http://hdl.handle.net/10400.23/451
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv Cancer Genet Cytogenet. 2008;180(1):14-9.
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dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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