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中国汉族人群中结直肠癌标签多态性的研究。

Investigation of tagging polymorphisms with colorectal cancer in Chinese Han population.

作者信息

Zhang Sheng, Chen Shuchen, Chen Yu, Kang Mingqiang, Liu Chao, Qiu Hao, Wang Yafeng, Tang Weifeng

机构信息

Department of General Surgery, Changzhou No. 3 People's Hospital, Changzhou, Jiangsu Province, China.

Department of Thoracic Surgery, Affiliated Union Hospital of Fujian Medical University, Fuzhou, Fujian Province, China.

出版信息

Oncotarget. 2017 Jun 29;8(38):63518-63527. doi: 10.18632/oncotarget.18845. eCollection 2017 Sep 8.

Abstract

The aim of this case-control study was to assess the relationship between the tagging polymorphisms in () gene and the susceptibility to colorectal cancer (CRC) in a Chinese Han population. A custom-by-design 48-Plex SNPscan Kit was used to determine the genotypes of rs3753584 T>C, rs9651118 T>C, rs1801133 G>A, rs4846048 A>G and rs4845882 G>A polymorphisms in 387 CRC patients and 1,536 non-cancer controls. The results revealed that rs1801133 G>A polymorphism was associated with a decreased risk of overall CRC. While rs4845882 G>A polymorphism conferred an increased risk to overall CRC. In a stratified analysis by CRC region, we found rs3753584 T>C and rs9651118 T>C polymorphisms were associated with the increased risk of colon cancer. In addition, a significantly increased risk of rectum cancer associated with rs3753584 T>C polymorphism was overt. However, rs1801133 G>A polymorphism conferred a decreased risk to colon cancer. In conclusion, findings of the present study reveal that the tagging polymorphisms in gene (rs3753584 T>C, rs9651118 T>C and rs4845882 G>A) are associated with the increased risk of CRC. However, rs1801133 G>A polymorphism confers a decreased risk to CRC. Additional studies with larger sample size are needed to confirm these findings.

摘要

本病例对照研究的目的是评估()基因中的标签多态性与中国汉族人群患结直肠癌(CRC)易感性之间的关系。使用定制的48重SNPscan试剂盒来确定387例CRC患者和1536例非癌症对照中rs3753584 T>C、rs9651118 T>C、rs1801133 G>A、rs4846048 A>G和rs4845882 G>A多态性的基因型。结果显示,rs1801133 G>A多态性与总体CRC风险降低相关。而rs4845882 G>A多态性使总体CRC风险增加。在按CRC部位进行的分层分析中,我们发现rs3753584 T>C和rs9651118 T>C多态性与结肠癌风险增加相关。此外,rs3753584 T>C多态性与直肠癌风险显著增加相关。然而,rs1801133 G>A多态性使结肠癌风险降低。总之,本研究结果表明,基因中的标签多态性(rs3753584 T>C、rs9651118 T>C和rs4845882 G>A)与CRC风险增加相关。然而,rs1801133 G>A多态性使CRC风险降低。需要更多大样本量的研究来证实这些发现。

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