Germline Variants and Genetic Interactions of Several EMT Regulatory Genes Increase the Risk of HBV-Related Hepatocellular Carcinoma

被引:2
|
作者
Liu, Wen-Xuan [1 ,2 ]
Yang, Lei [1 ,2 ]
Yan, Hui-Min [3 ]
Yan, Li-Na [1 ,2 ]
Zhang, Xiao-Lin [1 ,2 ]
Ma, Ning [2 ,4 ]
Tang, Long-Mei [1 ,2 ]
Gao, Xia [1 ,2 ]
Liu, Dian-Wu [1 ,2 ]
机构
[1] Hebei Med Univ, Sch Publ Hlth, Dept Epidemiol & Stat, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Sch Publ Hlth, Hebei Prov Key Lab Environm & Human Hlth, Shijiazhuang, Hebei, Peoples R China
[3] Shijiazhuang Fifth Hosp, Dept Lab Med, Shijiazhuang, Hebei, Peoples R China
[4] Hebei Med Univ, Sch Publ Hlth, Dept Social Med & Hlth Care Management, Shijiazhuang, Hebei, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
基金
中国国家自然科学基金;
关键词
hepatocellular carcinoma; epithelial-mesenchymal transition; polymorphisms; interaction; multifactor dimensionality reduction; EPITHELIAL-MESENCHYMAL TRANSITION; SNAIL EXPRESSION; CHEMORESISTANCE; METASTASIS; TWIST; GEMCITABINE; ACTIVATION; RESISTANCE; CELLS;
D O I
10.3389/fonc.2021.564477
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epithelial-mesenchymal transition (EMT) plays an important role in the development of hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC). We hypothesized that germline variants in the major EMT regulatory genes (SNAIL1, ZEB1, ZEB2, TWIST1) may influence the development of HBV-related HCC. We included 421 cases of HBsAg-positive patients with HCC, 1371 cases of HBsAg-positive subjects without HCC [patients with chronic hepatitis B (CHB) or liver cirrhosis (LC)] and 618 cases of healthy controls in the case-control study. Genotype, allele, and haplotype associations in the major EMT regulatory genes were tested. Environment-gene and gene-gene interactions were analysed using the non-parametric model-free multifactor dimensionality reduction (MDR) method. The SNAIL1rs4647958T>C was associated with a significantly increased risk of both HCC (CT+CC vs. TT: OR=1.559; 95% confidence interval [CI], 1.073-2.264; P=0.020) and CHB+LC (CT+CC vs. TT: OR=1.509; 95% CI, 1.145-1.988; P=0.003). Carriers of the TWIST1rs2285681G>C (genotypes CT+CC) had an increased risk of HCC (CG+CC vs. GG: OR=1.407; 95% CI, 1.065-1.858; P=0.016). The ZEB2rs3806475T>C was associated with significantly increased risk of both HCC (P (recessive) =0.001) and CHB+LC (P (recessive)<0.001). The CG haplotype of the rs4647958/rs1543442 haplotype block was associated with significant differences between healthy subjects and HCC patients (P=0.0347). Meanwhile, the CT haplotype of the rs2285681/rs2285682 haplotype block was associated with significant differences between CHB+LC and HCC patients (P=0.0123). In MDR analysis, the combination of TWIST1rs2285681, ZEB2rs3806475, SNAIL1rs4647958 exhibited the most significant association with CHB+LC and Health control in the three-locus model. Our results suggest significant single-gene associations and environment-gene/gene-gene interactions of EMT-related genes with HBV-related HCC.
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页数:11
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