Quantificação de DNA plasmático em pacientes com cancro da mama

Detalhes bibliográficos
Autor(a) principal: Ferreira, Maria Manuel da Silva
Data de Publicação: 2006
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10216/22401
Resumo: Breast cancer is the leading cause of cancer death in women worldwide. The purpose of our study was to determine whether the amounts of circulating DNA could discriminate between breast cancer patients and healthy individuals by using real-time PCR based DNA quantification methodology and determine the kinetics of circulating plasma DNA in surgically treated patients. Our standard protocol for quantification of cell free plasma DNA involved 175 consecutive patients with breast cancer and 80 healthy controls. The quantification was perfomed by real-time PCR amplification of the human telomerase reverse transcriptase gene (hTERT). We found increased levels of circulating DNA in breast cancer patients compared to control individuals (105.2 vs 77.06 ng/ml, p<0.001). We also found statistically significant differences in circulating DNA amounts in patients before and after breast surgery (105.2 vs 59.0 ng/ml, p=0.001). Increased plasma cell free DNA concentration was a strong risk factor for the presence of breast cancer, conferring an increased risk for the development of this disease (OR, 12.32; 95% CI, 2.09 52.28; p<0.001). High levels of plasma DNA were also correlated with a decrease in patients overall survival. There were no association between clinicopathological parameters and concentrations of cell free circulating DNA. In conclusion, cell-free DNA is significantly increased in plasma of breast cancer patients, which is associated with an increased risk for the presence of this disease and decrease of patient s survival. Therefore, quantification of circulating DNA by real-time PCR may be a good and simple tool for early detection of breast cancer with potential to clinical applicability together with other current methods used for monitoring the disease.
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spelling Quantificação de DNA plasmático em pacientes com cancro da mamaOncologia MolecularPortoBreast cancer is the leading cause of cancer death in women worldwide. The purpose of our study was to determine whether the amounts of circulating DNA could discriminate between breast cancer patients and healthy individuals by using real-time PCR based DNA quantification methodology and determine the kinetics of circulating plasma DNA in surgically treated patients. Our standard protocol for quantification of cell free plasma DNA involved 175 consecutive patients with breast cancer and 80 healthy controls. The quantification was perfomed by real-time PCR amplification of the human telomerase reverse transcriptase gene (hTERT). We found increased levels of circulating DNA in breast cancer patients compared to control individuals (105.2 vs 77.06 ng/ml, p<0.001). We also found statistically significant differences in circulating DNA amounts in patients before and after breast surgery (105.2 vs 59.0 ng/ml, p=0.001). Increased plasma cell free DNA concentration was a strong risk factor for the presence of breast cancer, conferring an increased risk for the development of this disease (OR, 12.32; 95% CI, 2.09 52.28; p<0.001). High levels of plasma DNA were also correlated with a decrease in patients overall survival. There were no association between clinicopathological parameters and concentrations of cell free circulating DNA. In conclusion, cell-free DNA is significantly increased in plasma of breast cancer patients, which is associated with an increased risk for the presence of this disease and decrease of patient s survival. Therefore, quantification of circulating DNA by real-time PCR may be a good and simple tool for early detection of breast cancer with potential to clinical applicability together with other current methods used for monitoring the disease.Faculdade de Medicina da Universidade do PortoFMUP20062011-02-07T00:00:00Z2011-02-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/mswordapplication/mswordapplication/mswordapplication/mswordapplication/mswordapplication/mswordapplication/mswordhttp://hdl.handle.net/10216/22401porFerreira, Maria Manuel da Silvainfo: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:RCAAP2023-11-29T15:56:46Zoai:repositorio-aberto.up.pt:10216/22401Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:35:39.886331Repositório 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 Quantificação de DNA plasmático em pacientes com cancro da mama
title Quantificação de DNA plasmático em pacientes com cancro da mama
spellingShingle Quantificação de DNA plasmático em pacientes com cancro da mama
Ferreira, Maria Manuel da Silva
Oncologia Molecular
Porto
title_short Quantificação de DNA plasmático em pacientes com cancro da mama
title_full Quantificação de DNA plasmático em pacientes com cancro da mama
title_fullStr Quantificação de DNA plasmático em pacientes com cancro da mama
title_full_unstemmed Quantificação de DNA plasmático em pacientes com cancro da mama
title_sort Quantificação de DNA plasmático em pacientes com cancro da mama
author Ferreira, Maria Manuel da Silva
author_facet Ferreira, Maria Manuel da Silva
author_role author
dc.contributor.author.fl_str_mv Ferreira, Maria Manuel da Silva
dc.subject.por.fl_str_mv Oncologia Molecular
Porto
topic Oncologia Molecular
Porto
description Breast cancer is the leading cause of cancer death in women worldwide. The purpose of our study was to determine whether the amounts of circulating DNA could discriminate between breast cancer patients and healthy individuals by using real-time PCR based DNA quantification methodology and determine the kinetics of circulating plasma DNA in surgically treated patients. Our standard protocol for quantification of cell free plasma DNA involved 175 consecutive patients with breast cancer and 80 healthy controls. The quantification was perfomed by real-time PCR amplification of the human telomerase reverse transcriptase gene (hTERT). We found increased levels of circulating DNA in breast cancer patients compared to control individuals (105.2 vs 77.06 ng/ml, p<0.001). We also found statistically significant differences in circulating DNA amounts in patients before and after breast surgery (105.2 vs 59.0 ng/ml, p=0.001). Increased plasma cell free DNA concentration was a strong risk factor for the presence of breast cancer, conferring an increased risk for the development of this disease (OR, 12.32; 95% CI, 2.09 52.28; p<0.001). High levels of plasma DNA were also correlated with a decrease in patients overall survival. There were no association between clinicopathological parameters and concentrations of cell free circulating DNA. In conclusion, cell-free DNA is significantly increased in plasma of breast cancer patients, which is associated with an increased risk for the presence of this disease and decrease of patient s survival. Therefore, quantification of circulating DNA by real-time PCR may be a good and simple tool for early detection of breast cancer with potential to clinical applicability together with other current methods used for monitoring the disease.
publishDate 2006
dc.date.none.fl_str_mv 2006
2011-02-07T00:00:00Z
2011-02-07
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dc.publisher.none.fl_str_mv Faculdade de Medicina da Universidade do Porto
FMUP
publisher.none.fl_str_mv Faculdade de Medicina da Universidade do Porto
FMUP
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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