Tagging polymorphisms of methyl-CpG binding domain 4 and gastric cardiac adenocarcinoma risk in a Chinese population

被引:0
|
作者
Wang, Xu [1 ]
Dong, Changqing [1 ]
Yin, Jun [2 ]
Tang, Weifeng [2 ]
Shen, Zhenya [1 ]
机构
[1] Soochow Univ, Dept Cardiovasc Surg, Affiliated Hosp 1, Inst Cardiovasc Sci, Suzhou 215006, Jiangsu, Peoples R China
[2] Jiangsu Univ, Dept Cardiothorac Surg, Affiliated Peoples Hosp, Zhenjiang, Jiangsu, Peoples R China
来源
DISEASES OF THE ESOPHAGUS | 2017年 / 30卷 / 02期
关键词
adenocarcinoma; gastric cardiac; MBD4; molecular epidemiology; polymorphisms; MISMATCH REPAIR; MICROSATELLITE INSTABILITY; GLU346LYS POLYMORPHISM; FRAMESHIFT MUTATIONS; GLYCOSYLASE MBD4; DNA-DAMAGE; GENE; MED1; CANCER; DEFICIENCY;
D O I
10.1111/dote.12500
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Potential effects of genetic factors on carcinogenesis of gastric cardiac adenocarcinoma (GCA) may exist. The present experiment specifically evaluated the genetic influence of single nucleotide in methyl-CpG binding domain 4 (MBD4) onGCA tumorigenesis. A case-control experiment based on hospital recruited 330 GCA patients and 608 non-cancer patients was carried out. We employed ligation detection reaction method to detect the genotypes. The results revealed that MBD4 rs3138373, rs2005618, and rs3138355 mutations had no significant association with the risk of GCA. However, a lower risk of GCA presented in male patients who carried the MBD4 rs3138355 G>A polymorphic loci by the stratified analyses. In general, The MBD4 gene polymorphism could not influence GCA hereditary predisposition. Nevertheless, whether the finding learned fromour experiment could apply to other ethnic groups will remain vague until future multicenter studies further test and verify our conclusions.
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页数:7
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