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首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >The relationship between three heat shock protein 70 gene polymorphisms and susceptibility to lung cancer.
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The relationship between three heat shock protein 70 gene polymorphisms and susceptibility to lung cancer.

机译:三种热休克蛋白70基因多态性与肺癌易感性的关系。

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BACKGROUND: Heat shock protein 70 (Hsp70) has been shown to act as a chaperone and be associated with a variety of tumors. We investigated HSP70-1 G+190C, HSP70-2 A+1267G, and HSP70-hom T+2437C polymorphisms to assess whether genetic variation in HSP70 plays a role in the occurrence and development of lung cancer. METHODS: A case-control study was conducted using 159 patients with lung cancer and 202 control subjects. Genomic DNA was typed for HSP70 polymorphisms using polymerase chain reactions with restriction fragment length polymorphism (PCR-RFLP). Unconditional logistic regression was used to estimate the relative risks of lung cancer. RESULTS: There were significant differences in genotype and allele distributions between patients and controls for the HSP70-1 G+190C polymorphisms with and without adjustment for age, gender, smoking history, drinking history and family history of cancer (p<0.05). No significant differences were found in the polymorphisms of HSP70-2 A+1267G and HSP70-hom T+2437C. The haplotype analysis showed that the G/A/C and C/G/T haplotypes were associated with a significantly increased risk of lung cancer compared to the G/G/T haplotype. After adjustments for other risk factors, such as age, gender, drinking history and family history of cancer, the interactions between the HSP70-1 and HSP70-hom genotypes and smoking were confirmed [I(AB), 2.56 and 5.12, respectively]. CONCLUSIONS: HSP70-1 G+190C may be a functional polymorphism and affect susceptibility to lung cancer, and homozygous C/C genotype may enhance the risk of lung cancer. In addition, smoking along with HSP70-1 G+190C and HSP70-hom T+2437C, may increase the risk of lung cancer.
机译:背景:热休克蛋白70(Hsp70)已被证明可以充当伴侣并与多种肿瘤有关。我们调查了HSP70-1 G + 190C,HSP70-2 A + 1267G和HSP70-hom T + 2437C多态性,以评估HSP70中的遗传变异是否在肺癌的发生和发展中起作用。方法:进行了一项病例对照研究,研究对象为159例肺癌患者和202例对照受试者。使用具有限制性片段长度多态性(PCR-RFLP)的聚合酶链式反应对HSP70多态性的基因组DNA进行分型。使用无条件逻辑回归来估计肺癌的相对风险。结果:HSP70-1 G + 190C基因多态性在患者和对照之间的基因型和等位基因分布之间存在显着差异,且不考虑年龄,性别,吸烟史,饮酒史和癌症家族史的调整(p <0.05)。在HSP70-2 A + 1267G和HSP70-hom T + 2437C的多态性上没有发现显着差异。单倍型分析显示,与G / G / T单倍型相比,G / A / C和C / G / T单倍型与肺癌风险显着增加有关。在调整了其他危险因素(例如年龄,性别,饮酒史和癌症家族史)后,确定了HSP70-1和HSP70-hom基因型与吸烟之间的相互作用[分别为I(AB),2.56和5.12]。结论:HSP70-1 G + 190C可能是功能性多态性并影响肺癌的易感性,纯合的C / C基因型可能会增加患肺癌的风险。此外,与HSP70-1 G + 190C和HSP70-hom T + 2437C一起吸烟可能会增加患肺癌的风险。

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