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胱天蛋白酶8(CASP8)启动子区的一个六核苷酸插入-缺失多态性与膀胱癌的风险及进展相关。

A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter associated with risk and progression of bladder cancer.

作者信息

Wang Meilin, Zhang Zhizhong, Tian Yuanyuan, Shao Jianfeng, Zhang Zhengdong

机构信息

Department of Molecular and Genetic Toxicology and Epidemiology and Biostatistics, Cancer Center of Nanjing Medical University, Nanjing, People's Republic of China.

出版信息

Clin Cancer Res. 2009 Apr 1;15(7):2567-72. doi: 10.1158/1078-0432.CCR-08-2829. Epub 2009 Mar 10.

Abstract

PURPOSE

Caspase-8 (CASP8) is a key regulator of apoptosis or programmed cell death, an essential defense mechanism against hyperproliferation and malignancy. We hypothesized that the variants in the CASP8 gene are associated with risk of bladder cancer.

EXPERIMENTAL DESIGN

In a hospital-based case-control study of 365 case patients with newly diagnosed bladder transitional cell carcinoma and 368 cancer-free controls frequency-matched by age and sex, we genotyped the functional -652 6N ins/del polymorphism (rs3834129) in the promoter of CASP8 and assessed its associations with risk of bladder cancer and interaction with tobacco smoking.

RESULTS

A significant decreased risk of bladder cancer was found for the CASP8 -652 6N ins/del (adjusted odds ratio, 0.72; 95% confidence interval, 0.53-0.99) and del/del (odds ratio, 0.37; 95% confidence interval, 0.18-0.77) genotypes. Furthermore, a significant additive interaction between CASP8 polymorphism and tobacco smoking on bladder cancer risk was observed.

CONCLUSIONS

These results suggested that the CASP8 -652 6N ins/del polymorphism is involved in etiology of bladder cancer and thus may be a marker for genetic susceptibility to bladder cancer in Chinese populations. Larger studies are warranted to validate our findings.

摘要

目的

半胱天冬酶8(CASP8)是细胞凋亡或程序性细胞死亡的关键调节因子,是对抗细胞过度增殖和恶性肿瘤的重要防御机制。我们推测CASP8基因变异与膀胱癌风险相关。

实验设计

在一项基于医院的病例对照研究中,对365例新诊断的膀胱移行细胞癌患者和368例年龄和性别频率匹配的无癌对照进行研究,我们对CASP8启动子中的功能性-652 6N插入/缺失多态性(rs3834129)进行基因分型,并评估其与膀胱癌风险的关联以及与吸烟的相互作用。

结果

发现CASP8 -652 6N插入/缺失(校正比值比,0.72;95%置信区间,0.53 - 0.99)和缺失/缺失(比值比,0.37;95%置信区间,0.18 - 0.77)基因型的膀胱癌风险显著降低。此外,观察到CASP8多态性与吸烟之间对膀胱癌风险存在显著的相加相互作用。

结论

这些结果表明,CASP8 -652 6N插入/缺失多态性参与膀胱癌的病因学,因此可能是中国人群膀胱癌遗传易感性的一个标志物。需要更大规模的研究来验证我们的发现。

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