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NFKB1 基因启动子-94ins/del ATTG 多态性与中国人群膀胱癌风险相关。

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

机构信息

Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

PLoS One. 2013 Aug 20;8(8):e71604. doi: 10.1371/journal.pone.0071604. eCollection 2013.

Abstract

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), grade 1 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.

摘要

背景

NFKB1 基因启动子中的功能-94 插入/缺失多态性(rs28362491)被报道会影响 NFKB1 的表达并易患不同类型的癌症。本研究旨在确定该多态性是否与膀胱癌风险相关。

材料和方法

在中国人群中,使用 TaqMan 分析检测 609 例病例和 640 例对照的基因型。使用 logistic 回归评估该多态性与膀胱癌风险之间的关联,使用实时定量聚合酶链反应确定 NFKB1 mRNA 的表达。

结果

与 ins/ins/ins/del 基因型相比,del/del 基因型与膀胱癌风险显著增加相关[调整后的比值比(OR)=1.92,95%置信区间(CI)=1.42-2.59]。该风险在 65 岁以上的人群(OR=2.37,95%CI=1.52-3.70)、男性(OR=1.97,95%CI=1.40-2.79)和有癌症家族史的人群(OR=3.59,95%CI=1.19-10.9)中更为明显。此外,该多态性与非肌肉浸润性膀胱癌(OR=2.07,95%CI=1.51-2.85)、1 级膀胱癌(OR=2.40,95%CI=1.68-3.43)、单发肿瘤膀胱癌(OR=2.04,95%CI=1.48-2.82)和肿瘤较小的膀胱癌(OR=2.10,95%CI=1.51-2.92)的发病风险增加相关。NFKB1 启动子中杂合插入基因型的膀胱癌组织中 NFKB1 mRNA 的表达高于缺失等位基因。

结论

总之,NFKB1 启动子中的-94 ins/del ATTG 多态性可能导致中国人群膀胱癌的病因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecb0/3748046/217e94bca389/pone.0071604.g001.jpg

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