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DNA修复基因多态性与肾细胞癌发生发展的关联

The association of DNA repair gene polymorphisms with the development and progression of renal cell carcinoma.

作者信息

Sakano S, Hinoda Y, Okayama N, Kawai Y, Korenaga Y, Eguchi S, Nagao K, Ohmi C, Naito K

机构信息

Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, Japan.

出版信息

Ann Oncol. 2007 Nov;18(11):1817-27. doi: 10.1093/annonc/mdm337. Epub 2007 Aug 21.

Abstract

BACKGROUND

DNA repair enzymes repair some of the DNA damage associated with risk factors for renal cell carcinoma (RCC), including smoking. DNA repair gene polymorphisms modulate the repair capacity and might influence individual risk and progression of RCC. We examined associations between functional polymorphisms and risk, clinicopathologic characteristics and survival of RCC.

PATIENTS AND METHODS

The study groups comprised 215 RCC patients and 215 age- and gender-matched healthy controls. Polymorphisms in xeroderma pigmentosum complementation groups C, D and G and X-ray repair cross-complementing groups 1 and 3 genes were genotyped.

RESULTS

No significant differences in DNA repair genotype were observed between RCC cases and controls. In all patients, however, greater numbers (> or =3) of total variant alleles in all DNA repair genes studied were associated with less frequent venous extension (P = 0.0079). In smokers, some genotypes were associated with characteristics of RCC (Ps < or = 0.0067) and smokers with greater numbers of total variant alleles had improved overall survival (P = 0.040).

CONCLUSION

These results suggest that DNA repair gene polymorphisms may not influence RCC susceptibility, but that some of them may influence RCC progression, especially in smokers, possibly due to altered DNA repair capacity by these polymorphisms.

摘要

背景

DNA修复酶可修复一些与肾细胞癌(RCC)风险因素相关的DNA损伤,包括吸烟。DNA修复基因多态性可调节修复能力,并可能影响RCC的个体风险和进展。我们研究了功能性多态性与RCC风险、临床病理特征及生存之间的关联。

患者与方法

研究组包括215例RCC患者以及215例年龄和性别匹配的健康对照。对着色性干皮病C、D和G互补组以及X线修复交叉互补组1和3基因的多态性进行基因分型。

结果

RCC病例与对照之间在DNA修复基因型上未观察到显著差异。然而,在所有患者中,所研究的所有DNA修复基因中总变异等位基因数量较多(≥3个)与静脉蔓延频率较低相关(P = 0.0079)。在吸烟者中,某些基因型与RCC特征相关(P≤0.0067),且总变异等位基因数量较多的吸烟者总生存期有所改善(P = 0.040)。

结论

这些结果表明,DNA修复基因多态性可能不影响RCC易感性,但其中一些可能影响RCC进展,尤其是在吸烟者中,这可能是由于这些多态性改变了DNA修复能力。

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