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在碳转移途径中的 TYMS 基因变异与卵巢癌协会联盟的卵巢癌类型有关。

Genetic variation in TYMS in the one-carbon transfer pathway is associated with ovarian carcinoma types in the Ovarian Cancer Association Consortium.

机构信息

Department of Population Health Research, Alberta Health Services-Cancer Care, 1331 29th Street Northwest, Calgary, Alberta T2N4N2, Canada.

出版信息

Cancer Epidemiol Biomarkers Prev. 2010 Jul;19(7):1822-30. doi: 10.1158/1055-9965.EPI-09-1317. Epub 2010 Jun 22.

Abstract

BACKGROUND

We previously reported the risks of ovarian carcinoma for common polymorphisms in one-carbon transfer genes. We sought to replicate associations for DPYD rs1801265, DNMT3A rs13420827, MTHFD1 rs1950902, MTHFS rs17284990, and TYMS rs495139 with risk of ovarian carcinoma overall and to use the large sample of assembled cases to investigate associations by histologic type.

METHODS

Associations were evaluated in the Ovarian Cancer Association Consortium, including 16 studies of 5,593 epithelial ovarian carcinoma cases and 9,962 controls of white non-Hispanic origin. Odds ratios (OR) and 95% confidence intervals (CI) were adjusted for age and study site.

RESULTS

The five polymorphisms were not associated with ovarian carcinoma overall (P(trend) > 0.13); however, associations for the minor allele at TYMS rs495139 were observed for carcinomas of mucinous type (OR, 1.19; 95% CI, 1.03-1.39; P = 0.02), clear cell type (OR, 0.86; 95% CI, 0.75-0.99; P = 0.04), and endometrioid type (OR, 0.90; 95% CI, 0.81-0.99; P = 0.04; P(heterogeneity) = 0.001). Restriction to low-grade mucinous carcinomas further strengthened the association for the mucinous type (OR, 1.32; 95% CI, 1.07-1.62; P = 0.01). TYMS rs495139 was not associated with serous type (OR, 1.06; 95% CI, 1.00-1.13; P = 0.05).

CONCLUSIONS

TYMS rs495139 may be associated with a differential risk of ovarian carcinoma types, indicating the importance of accurate histopathologic classification.

IMPACT

Biomarkers that distinguish ovarian carcinoma types are few, and TYMS rs495139 may provide a novel clue to type etiology.

摘要

背景

我们之前报道了常见的一碳转移基因多态性与卵巢癌风险的关系。我们试图复制 DPYD rs1801265、DNMT3A rs13420827、MTHFD1 rs1950902、MTHFS rs17284990 和 TYMS rs495139 与卵巢癌总体风险的关联,并利用大量已组装病例来按组织学类型调查关联。

方法

卵巢癌协会联盟中的 16 项研究包括 5593 例上皮性卵巢癌病例和 9962 例白色非西班牙裔起源的对照组,评估了这些关联。优势比(OR)和 95%置信区间(CI)根据年龄和研究地点进行了调整。

结果

这五个多态性与卵巢癌总体无关(P(趋势)>0.13);然而,TYMS rs495139 中的次要等位基因与黏液型癌(OR,1.19;95%CI,1.03-1.39;P=0.02)、透明细胞癌(OR,0.86;95%CI,0.75-0.99;P=0.04)和子宫内膜样癌(OR,0.90;95%CI,0.81-0.99;P=0.04;P(异质性)=0.001)有关。限制为低级别黏液性癌进一步加强了与黏液型癌的关联(OR,1.32;95%CI,1.07-1.62;P=0.01)。TYMS rs495139 与浆液型癌无关(OR,1.06;95%CI,1.00-1.13;P=0.05)。

结论

TYMS rs495139 可能与卵巢癌类型的不同风险相关,表明准确的组织病理学分类的重要性。

影响

区分卵巢癌类型的生物标志物很少,而 TYMS rs495139 可能为类型病因学提供新线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/478e/3013232/33c5bf733305/nihms258964f1.jpg

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