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XRCC1 和 ADPRT 基因多态性与中国人群铂类化疗卵巢癌生存的关联。

Association between polymorphisms of XRCC1 and ADPRT genes and ovarian cancer survival with platinum-based chemotherapy in Chinese population.

机构信息

Department of Gynecologic Cancer, Shengjing Hospital of China Medical University, Shenyang, China.

出版信息

Mol Cell Biochem. 2013 Jan;372(1-2):27-33. doi: 10.1007/s11010-012-1442-4. Epub 2012 Sep 16.

Abstract

The role of DNA repair gene polymorphisms in cancer development, progression, and response to treatment has received increased attention. We conducted a prospective study to determine whether associations exist between two polymorphisms in XRCC1 and ADPRT and the outcomes of Chinese ovarian cancer patients treated with platinum-based chemotherapy. A total of 335 new cases of ovarian cancer were consecutively collected between May 2005 and May 2007. Follow-up lasted for 4 years, and the outcome measure was survival time. Individuals carrying XRCC1 194Trp/Trp had a longer survival time than did those with the Arg/Arg genotype. Similarly, those carrying XRCC1 399 Gln/Gln genotypes had 0.44-fold the risk of death than those with the Arg/Arg genotype. The combination of XRCC1 194 Trp allele and 399 Gln allele could decrease the death risk of ovarian cancer. In summary, this study is the first to evaluate the associations between polymorphisms in DNA repair gene polymorphism and the risk of ovarian cancer in Chinese population. Our study found a significant association between XRCC1 Arg399Gln and XRCC1 Arg194Trp polymorphism and the clinical outcome of ovarian cancer. Furthermore, studies with larger sample sizes are still needed to confirm these associations in Chinese population.

摘要

DNA 修复基因多态性在癌症的发生、发展和对治疗的反应中的作用受到了越来越多的关注。我们进行了一项前瞻性研究,以确定 XRCC1 和 ADPRT 中的两个多态性与接受铂类化疗的中国卵巢癌患者的结局之间是否存在关联。2005 年 5 月至 2007 年 5 月期间连续收集了 335 例新的卵巢癌病例。随访时间为 4 年,结局测量为生存时间。携带 XRCC1 194Trp/Trp 基因型的个体比携带 Arg/Arg 基因型的个体具有更长的生存时间。同样,携带 XRCC1 399Gln/Gln 基因型的个体的死亡风险是携带 Arg/Arg 基因型的个体的 0.44 倍。XRCC1 194Trp 等位基因和 399Gln 等位基因的组合可以降低卵巢癌的死亡风险。总之,这项研究首次评估了 DNA 修复基因多态性与中国人群卵巢癌风险之间的关联。我们的研究发现 XRCC1 Arg399Gln 和 XRCC1 Arg194Trp 多态性与卵巢癌的临床结局之间存在显著关联。然而,仍需要更大样本量的研究来在中国人群中证实这些关联。

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