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Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients
AIM: To investigate the associations of the genetic polymorphisms of vascular endothelial growth factor A (VEGF-A) -1498C>T and -634G>C, with the survival of patients with colorectal cancer (CRC). METHODS: A prospective cohort consisting of 131 Brazilians patients consecutively operated on wit...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314204/ https://www.ncbi.nlm.nih.gov/pubmed/28255429 http://dx.doi.org/10.4251/wjgo.v9.i2.78 |
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author | do Espírito Santo, Gilmar Ferreira Galera, Bianca Borsatto Duarte, Elisabeth Carmen Chen, Elisabeth Suchi Azis, Lenuce Damazo, Amilcar Sabino Saba, Gabriela Tognini de Sousa Gehrke, Flávia Guerreiro da Silva, Ismael Dale Cotrim Waisberg, Jaques |
author_facet | do Espírito Santo, Gilmar Ferreira Galera, Bianca Borsatto Duarte, Elisabeth Carmen Chen, Elisabeth Suchi Azis, Lenuce Damazo, Amilcar Sabino Saba, Gabriela Tognini de Sousa Gehrke, Flávia Guerreiro da Silva, Ismael Dale Cotrim Waisberg, Jaques |
author_sort | do Espírito Santo, Gilmar Ferreira |
collection | PubMed |
description | AIM: To investigate the associations of the genetic polymorphisms of vascular endothelial growth factor A (VEGF-A) -1498C>T and -634G>C, with the survival of patients with colorectal cancer (CRC). METHODS: A prospective cohort consisting of 131 Brazilians patients consecutively operated on with a curative intention as a result of sporadic colorectal carcinoma was studied. DNA was extracted from peripheral blood and its amplification and allelic discrimination for each genetic polymorphism was performed using the technique of polymerase chain reaction (PCR) in real-time. The real-time PCR technique was used to identify the VEGF-A -1498C>T (rs833031) and -634G>C (rs2010963) polymorphisms. Genotyping was validated for VEGF-A -1498C>T polymorphism in 129 patients and for VEGF-A -634G>C polymorphism in 118 patients. The analysis of association between categorical variables was performed using logistic regression, survival by Kaplan-Meier method and multivariate analysis by the Cox regression method. RESULTS: In the univariate analysis there was a significant association (OR = 0.32; P = 0.048) between genotype CC of the VEGF-A -1498C>T polymorphism and the presence of CRC liver metastasis. There was no association between VEGF-A -1498C>T polymorphism and VEGF-A -634G>C polymorphism with further clinical or anatomopathologic variables. The genotype CC of the VEGF-A -1498C>T polymorphism was significantly correlated with the 5-year survival (P = 0.032), but not significant difference (P = 0.27) was obtained with the VEGF-A -634G>C polymorphism with the 5-year survival in the univariate analysis. The genotype CT (HR = 2.79) and CC (HR = 4.67) of the polymorphism VEGF-A -1498C>T and the genotype CC (HR = 3.76) of the polymorphism VEGF-A -634C>G acted as an independent prognostic factor for the risk of death in CRC patients. CONCLUSION: The CT and CC genotypes of the VEGF-A -1498C>T and the CC genotype of the VEGF-A -634C>G polymorphisms are prognostic factors of survival in Brazilians patients with sporadic colorectal carcinoma. |
format | Online Article Text |
id | pubmed-5314204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-53142042017-03-02 Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients do Espírito Santo, Gilmar Ferreira Galera, Bianca Borsatto Duarte, Elisabeth Carmen Chen, Elisabeth Suchi Azis, Lenuce Damazo, Amilcar Sabino Saba, Gabriela Tognini de Sousa Gehrke, Flávia Guerreiro da Silva, Ismael Dale Cotrim Waisberg, Jaques World J Gastrointest Oncol Observational Study AIM: To investigate the associations of the genetic polymorphisms of vascular endothelial growth factor A (VEGF-A) -1498C>T and -634G>C, with the survival of patients with colorectal cancer (CRC). METHODS: A prospective cohort consisting of 131 Brazilians patients consecutively operated on with a curative intention as a result of sporadic colorectal carcinoma was studied. DNA was extracted from peripheral blood and its amplification and allelic discrimination for each genetic polymorphism was performed using the technique of polymerase chain reaction (PCR) in real-time. The real-time PCR technique was used to identify the VEGF-A -1498C>T (rs833031) and -634G>C (rs2010963) polymorphisms. Genotyping was validated for VEGF-A -1498C>T polymorphism in 129 patients and for VEGF-A -634G>C polymorphism in 118 patients. The analysis of association between categorical variables was performed using logistic regression, survival by Kaplan-Meier method and multivariate analysis by the Cox regression method. RESULTS: In the univariate analysis there was a significant association (OR = 0.32; P = 0.048) between genotype CC of the VEGF-A -1498C>T polymorphism and the presence of CRC liver metastasis. There was no association between VEGF-A -1498C>T polymorphism and VEGF-A -634G>C polymorphism with further clinical or anatomopathologic variables. The genotype CC of the VEGF-A -1498C>T polymorphism was significantly correlated with the 5-year survival (P = 0.032), but not significant difference (P = 0.27) was obtained with the VEGF-A -634G>C polymorphism with the 5-year survival in the univariate analysis. The genotype CT (HR = 2.79) and CC (HR = 4.67) of the polymorphism VEGF-A -1498C>T and the genotype CC (HR = 3.76) of the polymorphism VEGF-A -634C>G acted as an independent prognostic factor for the risk of death in CRC patients. CONCLUSION: The CT and CC genotypes of the VEGF-A -1498C>T and the CC genotype of the VEGF-A -634C>G polymorphisms are prognostic factors of survival in Brazilians patients with sporadic colorectal carcinoma. Baishideng Publishing Group Inc 2017-02-15 2017-02-15 /pmc/articles/PMC5314204/ /pubmed/28255429 http://dx.doi.org/10.4251/wjgo.v9.i2.78 Text en ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Observational Study do Espírito Santo, Gilmar Ferreira Galera, Bianca Borsatto Duarte, Elisabeth Carmen Chen, Elisabeth Suchi Azis, Lenuce Damazo, Amilcar Sabino Saba, Gabriela Tognini de Sousa Gehrke, Flávia Guerreiro da Silva, Ismael Dale Cotrim Waisberg, Jaques Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
title | Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
title_full | Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
title_fullStr | Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
title_full_unstemmed | Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
title_short | Prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
title_sort | prognostic significance of vascular endothelial growth factor polymorphisms in colorectal cancer patients |
topic | Observational Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314204/ https://www.ncbi.nlm.nih.gov/pubmed/28255429 http://dx.doi.org/10.4251/wjgo.v9.i2.78 |
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