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AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population

BACKGROUND: A functional -94 insertion/deletion polymorphism (rs28362491) in the promoter of the NFKB1 gene was reported to influence NFKB1 expression and confer susceptibility to different types of cancer. This study aims to determine whether the polymorphism is associated with risk of bladder canc...

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Autores principales: Li, Pengchao, Gu, Jinbao, Yang, Xiao, Cai, Hongzhou, Tao, Jun, Yang, Xuejian, Lu, Qiang, Wang, Zengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708321/
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s102
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author Li, Pengchao
Gu, Jinbao
Yang, Xiao
Cai, Hongzhou
Tao, Jun
Yang, Xuejian
Lu, Qiang
Wang, Zengjun
author_facet Li, Pengchao
Gu, Jinbao
Yang, Xiao
Cai, Hongzhou
Tao, Jun
Yang, Xuejian
Lu, Qiang
Wang, Zengjun
author_sort Li, Pengchao
collection PubMed
description BACKGROUND: A functional -94 insertion/deletion polymorphism (rs28362491) in the promoter of the NFKB1 gene was reported to influence NFKB1 expression and confer susceptibility to different types of cancer. This study aims to determine whether the polymorphism is associated with risk of bladder cancer. MATERIALS AND METHODS: TaqMan assay was used to determine genotype among 609 cases and 640 controls in a Chinese population. Logistic regression was used to assess the association between the polymorphism and bladder cancer risk, and quantitative real-time polymerase chain reaction was used to determine NFKB1 mRNA expression. RESULTS: Compared with the ins/ins/ins/del genotypes, the del/del genotype was associated with a significantly increased risk of bladder cancer [adjusted odd ratio (OR) =1.92, 95% confidence interval (CI), 1.42-2.59]. The increased risk was more prominent among subjects over 65 years old (OR =2.37, 95% CI, 1.52-3.70), male subjects (OR =1.97, 95% CI, 1.40-2.79) and subjects with self-reported family history of cancer (OR =3.59, 95% CI, 1.19-10.9). Furthermore, the polymorphism was associated with a higher risk of developing non-muscle invasive bladder cancer (OR =2.07, 95% CI, 1.51-2.85), grade1 bladder cancer (OR =2.40, 95% CI, 1.68-3.43), single tumor bladder cancer (OR =2.04, 95% CI =1.48-2.82) and smaller tumor size bladder cancer (OR =2.10, 95% CI, 1.51-2.92). The expression of NFKB1 mRNA in bladder cancer tissues with homozygous insertion genotype was higher than that with deletion allele. CONCLUSIONS: In conclusion, the -94 ins/del ATTG polymorphism in NFKB1 promoter may contribute to the etiology of bladder cancer in the Chinese population.
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spelling pubmed-47083212016-01-26 AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population Li, Pengchao Gu, Jinbao Yang, Xiao Cai, Hongzhou Tao, Jun Yang, Xuejian Lu, Qiang Wang, Zengjun Transl Androl Urol Abstract Publication Urology BACKGROUND: A functional -94 insertion/deletion polymorphism (rs28362491) in the promoter of the NFKB1 gene was reported to influence NFKB1 expression and confer susceptibility to different types of cancer. This study aims to determine whether the polymorphism is associated with risk of bladder cancer. MATERIALS AND METHODS: TaqMan assay was used to determine genotype among 609 cases and 640 controls in a Chinese population. Logistic regression was used to assess the association between the polymorphism and bladder cancer risk, and quantitative real-time polymerase chain reaction was used to determine NFKB1 mRNA expression. RESULTS: Compared with the ins/ins/ins/del genotypes, the del/del genotype was associated with a significantly increased risk of bladder cancer [adjusted odd ratio (OR) =1.92, 95% confidence interval (CI), 1.42-2.59]. The increased risk was more prominent among subjects over 65 years old (OR =2.37, 95% CI, 1.52-3.70), male subjects (OR =1.97, 95% CI, 1.40-2.79) and subjects with self-reported family history of cancer (OR =3.59, 95% CI, 1.19-10.9). Furthermore, the polymorphism was associated with a higher risk of developing non-muscle invasive bladder cancer (OR =2.07, 95% CI, 1.51-2.85), grade1 bladder cancer (OR =2.40, 95% CI, 1.68-3.43), single tumor bladder cancer (OR =2.04, 95% CI =1.48-2.82) and smaller tumor size bladder cancer (OR =2.10, 95% CI, 1.51-2.92). The expression of NFKB1 mRNA in bladder cancer tissues with homozygous insertion genotype was higher than that with deletion allele. CONCLUSIONS: In conclusion, the -94 ins/del ATTG polymorphism in NFKB1 promoter may contribute to the etiology of bladder cancer in the Chinese population. AME Publishing Company 2014-09 /pmc/articles/PMC4708321/ http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s102 Text en 2014 Translational Andrology and Urology. All rights reserved.
spellingShingle Abstract Publication Urology
Li, Pengchao
Gu, Jinbao
Yang, Xiao
Cai, Hongzhou
Tao, Jun
Yang, Xuejian
Lu, Qiang
Wang, Zengjun
AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population
title AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population
title_full AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population
title_fullStr AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population
title_full_unstemmed AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population
title_short AB102. Functional promoter-94 ins/del ATTG polymorphism in NFKB1 gene is associated with bladder cancer risk in a Chinese population
title_sort ab102. functional promoter-94 ins/del attg polymorphism in nfkb1 gene is associated with bladder cancer risk in a chinese population
topic Abstract Publication Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708321/
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s102
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