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Correlation between Bax gene polymorphisms and esophagus cancer

The present study investigated the association between the G(−248)A single nucleotide polymorphism (SNP) in the promoter region of B-cell lymphoma 2 (Bcl-2) associated X protein (Bax), which is a pro-apoptosis gene and the clinicopathological parameters and prognosis of patients with esophagus cance...

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Autores principales: Sun, Lei, Wei, Lingyun, Wei, Lei, Li, Demin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256320/
https://www.ncbi.nlm.nih.gov/pubmed/30546444
http://dx.doi.org/10.3892/ol.2018.9511
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author Sun, Lei
Wei, Lingyun
Wei, Lei
Li, Demin
author_facet Sun, Lei
Wei, Lingyun
Wei, Lei
Li, Demin
author_sort Sun, Lei
collection PubMed
description The present study investigated the association between the G(−248)A single nucleotide polymorphism (SNP) in the promoter region of B-cell lymphoma 2 (Bcl-2) associated X protein (Bax), which is a pro-apoptosis gene and the clinicopathological parameters and prognosis of patients with esophagus cancer. Three genotypes (AA, AG and GG) of Bax G(−248)A SNP were detected in 75 patients with esophageal squamous cell carcinoma (ESCC) via polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP). The expression of Bax in tumor tissues from 75 patients with ESCC and 30 para-carcinoma normal tissues were detected via immunohistochemistry. The association between the Bax protein expression and the Bax gene polymorphism was analyzed via the χ(2) test. The clinical data of patients was collected and the association between Bax gene polymorphism and the pathological parameters and the prognosis of patients with ESCC was analyzed. The PCR-RFLP results revealed that the number of cases and the distribution frequencies of GG, AG and AA genotypes of Bax polymorphism in patients with ESCC were 50 (66.67%), 16 (21.33%) and 9 (12%), respectively. The immunohistochemical results revealed that the positive expression rate of Bax in ESSC tissues was 42.67%. Bax protein expression was associated with the Bax gene polymorphism, which was associated with outer membrane infiltration, differentiation degree, lymphatic metastasis and the clinical staging of patients. The overall 5-year survival rate of patients was 38.6% (29/75). The survival analyses revealed that the prognosis of patients with AG+AA genotypes was favorable, while that of patients with GG genotype was poor. Bax gene polymorphism was associated with Bax gene expression, tumor staging and lymphatic metastasis in patients with ESCC, which is an influencing factor for the overall survival rate and may be used as a reference index for the prognosis evaluation of patients with ESCC.
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spelling pubmed-62563202018-12-13 Correlation between Bax gene polymorphisms and esophagus cancer Sun, Lei Wei, Lingyun Wei, Lei Li, Demin Oncol Lett Articles The present study investigated the association between the G(−248)A single nucleotide polymorphism (SNP) in the promoter region of B-cell lymphoma 2 (Bcl-2) associated X protein (Bax), which is a pro-apoptosis gene and the clinicopathological parameters and prognosis of patients with esophagus cancer. Three genotypes (AA, AG and GG) of Bax G(−248)A SNP were detected in 75 patients with esophageal squamous cell carcinoma (ESCC) via polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP). The expression of Bax in tumor tissues from 75 patients with ESCC and 30 para-carcinoma normal tissues were detected via immunohistochemistry. The association between the Bax protein expression and the Bax gene polymorphism was analyzed via the χ(2) test. The clinical data of patients was collected and the association between Bax gene polymorphism and the pathological parameters and the prognosis of patients with ESCC was analyzed. The PCR-RFLP results revealed that the number of cases and the distribution frequencies of GG, AG and AA genotypes of Bax polymorphism in patients with ESCC were 50 (66.67%), 16 (21.33%) and 9 (12%), respectively. The immunohistochemical results revealed that the positive expression rate of Bax in ESSC tissues was 42.67%. Bax protein expression was associated with the Bax gene polymorphism, which was associated with outer membrane infiltration, differentiation degree, lymphatic metastasis and the clinical staging of patients. The overall 5-year survival rate of patients was 38.6% (29/75). The survival analyses revealed that the prognosis of patients with AG+AA genotypes was favorable, while that of patients with GG genotype was poor. Bax gene polymorphism was associated with Bax gene expression, tumor staging and lymphatic metastasis in patients with ESCC, which is an influencing factor for the overall survival rate and may be used as a reference index for the prognosis evaluation of patients with ESCC. D.A. Spandidos 2018-12 2018-09-27 /pmc/articles/PMC6256320/ /pubmed/30546444 http://dx.doi.org/10.3892/ol.2018.9511 Text en Copyright: © Sun et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Sun, Lei
Wei, Lingyun
Wei, Lei
Li, Demin
Correlation between Bax gene polymorphisms and esophagus cancer
title Correlation between Bax gene polymorphisms and esophagus cancer
title_full Correlation between Bax gene polymorphisms and esophagus cancer
title_fullStr Correlation between Bax gene polymorphisms and esophagus cancer
title_full_unstemmed Correlation between Bax gene polymorphisms and esophagus cancer
title_short Correlation between Bax gene polymorphisms and esophagus cancer
title_sort correlation between bax gene polymorphisms and esophagus cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256320/
https://www.ncbi.nlm.nih.gov/pubmed/30546444
http://dx.doi.org/10.3892/ol.2018.9511
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