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基因中的遗传多态性是中国人罹患甲状腺癌的风险因素。

Genetic polymorphisms in the gene are risk factors for thyroid cancer in the Chinese population.

机构信息

Department of Otolaryngology Head & Neck Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, Shaanxi, China.

出版信息

Future Oncol. 2021 Dec;17(34):4677-4686. doi: 10.2217/fon-2021-0748. Epub 2021 Nov 8.

Abstract

Thyroid cancer is the most common endocrine malignancy and the fastest growing cancer worldwide. Thyroid cancer has the largest genetic component of all cancers. Previous genome-wide association studies indicated that genetic polymorphism in is related to thyroid cancer susceptibility in European populations. This study aims to determine the influence of polymorphisms on thyroid cancer risk in Chinese individuals. This case-control study identified four polymorphisms in among 510 thyroid cancer cases and 509 healthy controls. The associations of polymorphisms with thyroid cancer susceptibility were detected by calculating odds ratios. Multifactor dimensionality reduction was performed to detect the impact of SNP (single nucleotide polymorphism)-SNP interactions on the risk of thyroid cancer. The study showed that rs10910660 in was related to thyroid cancer susceptibility. Rs12129938 played a protective role in thyroid cancer susceptibility. Stratification analysis indicated that rs10910660 increased thyroid cancer risk at age >45 years. Rs12129938 enhanced susceptibility to thyroid cancer at age >45 years, while this SNP decreased thyroid cancer risk at age ≤45 years. Rs4649295 was associated with lower susceptibility to thyroid cancer at age ≤45 years. An association was observed between rs6424270 and rs12129938 with decreased susceptibility to thyroid cancer in women. Rs10910660 was related to thyroid cancer risk in men. The combination of rs6424270, rs10910660, rs12129938 and rs4649295 was the best model to predict thyroid cancer. This study suggests that polymorphisms are risk factors for thyroid cancer in the Chinese population.

摘要

甲状腺癌是最常见的内分泌恶性肿瘤,也是全球增长最快的癌症。甲状腺癌是所有癌症中遗传成分最大的。先前的全基因组关联研究表明, 中的遗传多态性与欧洲人群的甲状腺癌易感性有关。本研究旨在确定 多态性对中国人群甲状腺癌风险的影响。这项病例对照研究在 510 例甲状腺癌病例和 509 例健康对照中鉴定了 中的 4 个多态性。通过计算比值比来检测 多态性与甲状腺癌易感性的关联。多因子降维用于检测 SNP(单核苷酸多态性)-SNP 相互作用对甲状腺癌风险的影响。研究表明, 中的 rs10910660 与甲状腺癌易感性有关。rs12129938 对甲状腺癌易感性起保护作用。分层分析表明,rs10910660 增加了年龄 >45 岁的甲状腺癌风险。rs12129938 增强了年龄 >45 岁的甲状腺癌易感性,而该 SNP 降低了年龄 ≤45 岁的甲状腺癌风险。rs4649295 与年龄 ≤45 岁的甲状腺癌低易感性有关。rs6424270 与 rs12129938 与女性甲状腺癌易感性降低有关。rs10910660 与男性甲状腺癌风险有关。rs6424270、rs10910660、rs12129938 和 rs4649295 的组合是预测甲状腺癌的最佳模型。本研究表明, 多态性是中国人群甲状腺癌的危险因素。

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