检验医学 ›› 2017, Vol. 32 ›› Issue (1): 35-40.DOI: 10.3969/j.issn.1673-8640.2017.01.009

• 临床应用研究_论著 • 上一篇    下一篇

广西壮族人群TNF-α基因多态性及其表达与原发性肝细胞癌的相关性研究

李艳秋, 朱波, 欧超, 赵惠柳, 舒宏, 容敏华   

  1. 广西医科大学附属肿瘤医院检验科,广西 南宁 530021
  • 收稿日期:2016-04-06 出版日期:2017-01-20 发布日期:2017-02-10
  • 作者简介:null

    作者简介:李艳秋,女,1990年生,主要从事分子生物学研究。

    通信作者:朱 波,联系电话:0771-5605891。

  • 基金资助:
    广西自然科学基金项目(2012GXNSFAA053170)

Correlations of TNF-α gene polymorphism and its expression with primary hepatocellular carcinoma in Guangxi Zhuang population

LI Yanqiu, ZHU Bo, OU Chao, ZHAO Huiliu, SHU Hong, RONG Minhua   

  1. Department of Clinical Laboratory,Tumor Hospital of Guangxi Medical University,Nanning 530021,Guangxi,China
  • Received:2016-04-06 Online:2017-01-20 Published:2017-02-10

摘要:

目的 探讨肿瘤坏死因子TNF-α)-238/-308 2个位点的基因单核苷酸多态性(SNP)及血清TNF-α水平与广西壮族人群原发性肝细胞癌(HCC)的关系及其临床意义。方法 将175名研究对象分为HCC组102例和正常对照组73名,采用双抗体夹心酶联免疫吸附试验(ELISA)和聚合酶链反应-限制性内切酶长度多态性(PCR-RFLP)技术检测血清TNF-α水平并对TNF-α-308/-238 2个位点基因多态性进行分型。结果 HCC组血清TNF-α水平显著高于正常对照组(P<0.01),携带TNF-α-308 GA+AA基因型的个体血清TNF-α水平表达高于携带TNF-α-308 GG基因型个体(P<0.01)。HCC组TNF-α-308位点的基因型和等位基因频率均高于正常对照组(P<0.05),TNF-α-238位点的基因型和等位基因频率在HCC组和正常对照组中的分布差异均无统计学意义(P>0.05)。携带TNF-α-308位点GA或AA基因型的个体与携带GG基因型的个体相比发生肝癌的风险更高[比值比OR=3.556,95%可信区间(CI)1.581~7.994],携带TNF-α-308 A等位基因的个体患HCC的风险是携带G等位基因个体的3.153倍(OR=3.153,95%CI 1.465~6.784)。结论 HCC患者的血清TNF-α水平高于正常对照组。TNF-α-308位点多态性与血清TNF-α水平有关。TNF-α-308位点多态性可能与广西地区壮族人群HCC的遗传易感性有关。

关键词: 肿瘤坏死因子-α, 原发性肝细胞癌, 单核苷酸多态性, 易感性

Abstract:

Objective To investigate the correlations of tumor necrosis factor-alpha(TNF-α) -238/-308 single nucleotide polymorphism(SNP) and serum TNF-α levels with primary hepatocellular carcinoma (HCC) in Guangxi Zhuang population. Methods A total of 175 subjects were classified into primary HCC group(102 cases) and healthy control group(73 cases). Serum TNF-α levels and the genotypes of TNF-α-238/-308 SNP were determined by double antibody sandwich enzyme-linked immunosorbent assay(ELISA) and polymerase chain reaction(PCR)-restriction fragment length polymorphism(RFLP). Results Serum TNF-α levels in primary HCC group were higher than those in healthy control group(P<0.01). For the genotype of TNF-α-308,serum TNF-α level of GA+AA genotype was higher than that of GG genotype(P<0.01). The genotype and allele frequencies of TNF-α-308 in primary HCC group were higher than those in healthy control group(P<0.05). The genotype and allele frequencies of TNF-α-238 in primary HCC group and healthy control group had no statistical significance(P>0.05). The risk of primary HCC was higher in TNF-α-308 GA or AA genotype than that in TNF-α-308 GG genotype [odds ratio(OR)=3.556,95% confidence interval(CI)1.581-7.994]. The risk in TNF-α-308 A allele was 3.153 times higher than that in TNF-α-308 G allele (OR=3.153,95%CI 1.465-6.784). Conclusions Serum TNF-α levels in primary HCC group are higher than those in healthy control group. TNF-α-308 SNP are correlated to serum TNF-α levels. TNF-α-308 SNP may be correlated to the genetic susceptibility of primary HCC in Guangxi Zhuang population.

Key words: Tumor necrosis factor-alpha, Primary hepatocellular carcinoma, Single nucleotide polymorphism, Susceptibility

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