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Caspase 9 promoter polymorphisms and risk of primary lung cancer.

机译:Caspase 9启动子多态性与原发性肺癌的风险。

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摘要

Caspase-9 (CASP-9) is an initiator CASP in the apoptosome-driven apoptosis pathway and plays an important role in the development and progression of cancer. Polymorphisms in the promoter region of the CASP-9 gene may influence the promoter activity of this gene, thereby modulating susceptibility to lung cancer. To test this hypothesis, we examined the association of four polymorphisms [-1263A>G, -905T>G, -712C>T and -293_-275delCGTGAGGTCAGTGCGGGGA (-293del)] in the CASP-9 promoter with the risk of lung cancer in a Korean population. The CASP-9 genotypes were determined in 432 lung cancer patients and 432 healthy controls that were frequency-matched for age and gender. The -1263 GG genotype was associated with a significantly decreased risk of lung cancer compared with the -1263 AA genotype or combined -1263 AA+AG genotype [adjusted odds ratio (OR)=0.64, 95% confidence interval (95% CI)=0.42-0.98, P=0.04 and adjusted OR=0.67, 95% CI=0.46-0.97, P=0.01, respectively]. For the -712C>T polymorphism, individuals with at least one -712T allele were at a significantly increased risk of lung cancer compared with those harboring the -712 CC genotype (adjusted OR=1.42, 95% CI=1.06-1.89, P=0.02). Consistent with the results of genotype analyses, the -1263G/-712C (G-C) haplotype was associated with a significantly decreased risk of lung cancer [adjusted OR=0.59, 95% CI=0.47-0.75, P and Bonferroni corrected P (Pc)<0.001]. Moreover, the risk of lung cancer decreased in a dose-dependent manner as the number of the G-C haplotypes increased (adjusted OR=0.60, 95% CI=0.45-0.81, P=0.0007 and Pc=0.0014 for the G-C heterozygotes and adjusted OR=0.34, 95% CI=0.17-0.68, P=0.0023 and Pc=0.0046 for the G-C homozygotes; P(trend)<0.001). The promoter assay revealed the G-C haplotype to have a significantly higher promoter activity than the -1263G/-712T and -1263A/-712C haplotypes. These results suggest that CASP-9 promoter polymorphisms affect CASP-9 expression and contribute to genetic susceptibility to lung cancer.
机译:Caspase-9(CASP-9)是凋亡小体驱动的细胞凋亡途径中的启动子CASP,在癌症的发生和发展中起重要作用。 CASP-9基因启动子区域的多态性可能影响该基因的启动子活性,从而调节对肺癌的敏感性。为了验证该假设,我们研究了CASP-9启动子中四种多态性[-1263A> G,-905T> G,-712C> T和-293_-275delCGTGAGGTCAGTGCGGGGA(-293del)]与肺癌风险的相关性。韩国人在432例肺癌患者和432例健康对照中确定了CASP-9基因型,这些患者的年龄和性别均频率匹配。与-1263 AA基因型或组合的-1263 AA + AG基因型相比,-1263 GG基因型与肺癌风险显着降低[调整比值比(OR)= 0.64,95%置信区间(95%CI)= 0.42-0.98,P = 0.04,调整后的OR = 0.67,95%CI = 0.46-0.97,P = 0.01]。对于-712C> T多态性,至少具有-712T等位基因的个体与具有-712 CC基因型的个体相比,患肺癌的风险显着增加(调整后的OR = 1.42,95%CI = 1.06-1.89,P = 0.02)。与基因型分析结果一致,-1263G / -712C(GC)单倍型与肺癌风险显着降低有关[校正后的OR = 0.59、95%CI = 0.47-0.75,P和Bonferroni校正后的P(Pc) <0.001]。此外,随着GC单倍型数目的增加,肺癌的风险呈剂量依赖性降低(对于GC杂合子,校正后的OR = 0.60,95%CI = 0.45-0.81,P = 0.0007和Pc = 0.0014,校正后的OR对于GC纯合子,= 0.34,95%CI = 0.17-0.68,P = 0.0023和Pc = 0.0046; P(趋势)<0.001)。启动子分析显示,G-C单倍型比-1263G / -712T和-1263A / -712C单倍型具有显着更高的启动子活性。这些结果表明,CASP-9启动子多态性影响CASP-9的表达并有助于肺癌的遗传易感性。

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