Role of EZH2 Polymorphisms in Esophageal Squamous Cell Carcinoma Risk in Han Chinese Population

International Journal of Molecular Sciences

Zhen-Bin Ma¹  Ning Shi¹  Qiong Niu¹  Guang-Hong Guo² 

[1] Department of Gastroenterology, Affiliated Hospital of Binzhou Medical College, No. 661, Yellow-River Second Street, Binzhou 256600, Shandong, China;Department of Gynaecology, Affiliated Hospital of Binzhou Medical College, No. 661,Yellow-River Second Street, Binzhou 256600, Shandong, China;

关键词: allele;    EZH2;    esophageal squamous cell carcinoma;    polymorphism;   

DOI  :  10.3390/ijms150712688

来源: DOAJ

【 摘 要 】

Gene single nucleotide polymorphisms play a critical role in the development of esophageal squamous cell carcinoma (ESCC). The aim of this study is to investigate the associations between EZH2 gene polymorphisms and ESCC risk. We undertook a case-control study to analyze three EZH2 polymorphisms (148505302C > T, 2110 + 6A > C and626 − 394T > C) in an Han Chinese population, by extraction of genomic DNA from the peripheral blood of 476 patients with ESCC and 492 control participants, and performed EZH2 genotyping using DNA sequencing. The obtained results indicated that overall, no statistically significant association was observed in 148505302C > T and 2110 + 6A > C. However, 626 − 394T > C genotype was at increased risk of ESCCs (p = 0.006; odds ratio (OR) = 1.131, CI 95%: 1.034–1.236). Moreover, 626 − 394C/C genotype ESCCs weremore significantly common in patients with tumor size of >5 cm than T allele ESCC andin cases of poor differentiation and lower advanced pathological stage. In conclusion, polymorphism in 626 − 394T > C was observed to be associated with susceptibilityof ESCC. Nevertheless, further investigation with a larger sample size is needed to support our results.

【 授权许可】

Unknown