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Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor

BACKGROUND: Lung cancer is the most common second primary cancer. We investigated whether the TNF-α-308 and TNF-α-238 polymorphisms were associated with the susceptibility and severity of lung cancer as the second primary cancer (LC2). MATERIAL/METHODS: This study included 104 patients from the grou...

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Autores principales: Flego, Veljko, Ristić, Smiljana, Pavlić, Sanja Dević, Lender, Dubravka Matanić, Bulat-Kardum, Ljiljana, Kapović, Miljenko, Badovinac, Andjelka Radojčić
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3808239/
https://www.ncbi.nlm.nih.gov/pubmed/24113849
http://dx.doi.org/10.12659/MSM.889554
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author Flego, Veljko
Ristić, Smiljana
Pavlić, Sanja Dević
Lender, Dubravka Matanić
Bulat-Kardum, Ljiljana
Kapović, Miljenko
Badovinac, Andjelka Radojčić
author_facet Flego, Veljko
Ristić, Smiljana
Pavlić, Sanja Dević
Lender, Dubravka Matanić
Bulat-Kardum, Ljiljana
Kapović, Miljenko
Badovinac, Andjelka Radojčić
author_sort Flego, Veljko
collection PubMed
description BACKGROUND: Lung cancer is the most common second primary cancer. We investigated whether the TNF-α-308 and TNF-α-238 polymorphisms were associated with the susceptibility and severity of lung cancer as the second primary cancer (LC2). MATERIAL/METHODS: This study included 104 patients from the group LC2. The control subjects included 2 groups. The first control group (LC1) comprised 201 unrelated patients with lung cancer as a first primary cancer. The second control group (HC) comprised 230 healthy blood donors, matched for sex and age to the study group. RESULTS: The frequencies of the TNF-α-238 polymorphism GG genotype and the G allele were higher in the LC2 group than in the LC1 group, but the differences did not reach significance (p=0.054 and p=0.057, respectively). Similar differences were found in the TNF-α-238 polymorphism GG genotype and G allele between the LC2 group and the HC group (p=0.054 and p=0.057, respectively). In terms of the different types of lung cancer, patients with a second primary NSCLC (non-small cell lung cancer) more frequently had TNF-α-238 polymorphism GG genotypes and G alleles than patients with a first primary NSCLC (the differences approached statistical significance: p=0.060, p=0.064, respectively). All (100%) patients of group LC2 (n=104) had the GG genotype and the G allele. GG genotype was exclusive and no A allele was found in group LC2. CONCLUSIONS: TNF-α-238 polymorphism GG genotype and the G allele could have a promotional effect on the development of NSCLC in the group of patients with LC2.
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spelling pubmed-38082392013-10-28 Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor Flego, Veljko Ristić, Smiljana Pavlić, Sanja Dević Lender, Dubravka Matanić Bulat-Kardum, Ljiljana Kapović, Miljenko Badovinac, Andjelka Radojčić Med Sci Monit Clinical Research BACKGROUND: Lung cancer is the most common second primary cancer. We investigated whether the TNF-α-308 and TNF-α-238 polymorphisms were associated with the susceptibility and severity of lung cancer as the second primary cancer (LC2). MATERIAL/METHODS: This study included 104 patients from the group LC2. The control subjects included 2 groups. The first control group (LC1) comprised 201 unrelated patients with lung cancer as a first primary cancer. The second control group (HC) comprised 230 healthy blood donors, matched for sex and age to the study group. RESULTS: The frequencies of the TNF-α-238 polymorphism GG genotype and the G allele were higher in the LC2 group than in the LC1 group, but the differences did not reach significance (p=0.054 and p=0.057, respectively). Similar differences were found in the TNF-α-238 polymorphism GG genotype and G allele between the LC2 group and the HC group (p=0.054 and p=0.057, respectively). In terms of the different types of lung cancer, patients with a second primary NSCLC (non-small cell lung cancer) more frequently had TNF-α-238 polymorphism GG genotypes and G alleles than patients with a first primary NSCLC (the differences approached statistical significance: p=0.060, p=0.064, respectively). All (100%) patients of group LC2 (n=104) had the GG genotype and the G allele. GG genotype was exclusive and no A allele was found in group LC2. CONCLUSIONS: TNF-α-238 polymorphism GG genotype and the G allele could have a promotional effect on the development of NSCLC in the group of patients with LC2. International Scientific Literature, Inc. 2013-10-11 /pmc/articles/PMC3808239/ /pubmed/24113849 http://dx.doi.org/10.12659/MSM.889554 Text en © Med Sci Monit, 2013 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Clinical Research
Flego, Veljko
Ristić, Smiljana
Pavlić, Sanja Dević
Lender, Dubravka Matanić
Bulat-Kardum, Ljiljana
Kapović, Miljenko
Badovinac, Andjelka Radojčić
Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
title Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
title_full Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
title_fullStr Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
title_full_unstemmed Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
title_short Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
title_sort tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3808239/
https://www.ncbi.nlm.nih.gov/pubmed/24113849
http://dx.doi.org/10.12659/MSM.889554
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