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基因多态性与中国人群肝癌易感性的关系。

, , and Gene Polymorphisms on Hepatocellular Carcinoma Susceptibility in the Chinese Population.

机构信息

Department of Clinical Laboratory, The Affiliated Tumor Hospital of Guangxi Medical University, Nanning, 530021 Guangxi, China.

Department of Surgery, Maternal and Child Health Hospital of the Guangxi Zhuang Autonomous Region, Nanning, China.

出版信息

Biomed Res Int. 2020 Sep 29;2020:2918517. doi: 10.1155/2020/2918517. eCollection 2020.

Abstract

The interleukin- (IL-) 33/ axis plays a pivotal role in tumorigenesis through influencing cancer stemness and other mechanisms. is one of the critical markers of hepatocellular carcinoma (HCC) among the cancer stem cells (CSCs). There is still a lack of gene single-nucleotide polymorphisms (SNPs) combined with / pathway single-nucleotide polymorphisms in HCC susceptibility analysis literature, although and / have been reported separately in human cancers. This study is aimed at investigating the relationship between , , and SNPs and HCC susceptibility and clinicopathological features. We analyzed 565 HCC patients and 561 healthy controls in the Chinese population. The genes for rs187115A>G, rs1929992A>G, and rs3821204G>C were typed using the SNaPshot method. We found that the distribution frequencies of and alleles and genotypes in both the HCC case group and the control group were statistically significant ( < 0.05). The results showed that individuals carrying at least one G allele of the rs187115 gene were at a higher risk than the AA genotype carriers ( = 0.007, odds ratio (OR) = 1.429, 95% confidence interval (CI): 1.102-1.854). Similarly, individuals with at least one C allele of rs3821204 had a higher risk of HCC than those with GG genes ( ≤ 0.001, OR = 1.647, 95% CI: 1.296-2.093). Combining the haplotype analysis of the 3 loci suggested that rs187115, rs1929992, and rs3821204 are associated with the risk of HCC and could potentially serve as useful genetic markers for HCC in some populations of China.

摘要

白细胞介素- (IL-) 33/ 轴通过影响癌症干细胞特性和其他机制在肿瘤发生中发挥关键作用。 是肝癌 (HCC) 中癌症干细胞 (CSC) 的关键标志物之一。尽管已分别在人类癌症中报道了 和 / ,但在 HCC 易感性分析文献中仍缺乏 基因单核苷酸多态性 (SNP) 与 / 途径单核苷酸多态性的组合。本研究旨在探讨 、 和 基因 SNP 与 HCC 易感性和临床病理特征的关系。我们在中国人群中分析了 565 例 HCC 患者和 561 例健康对照者。采用 SNaPshot 方法对 rs187115A>G、rs1929992A>G 和 rs3821204G>C 基因进行分型。我们发现 HCC 病例组和对照组中 和 等位基因和基因型的分布频率均具有统计学意义 ( < 0.05)。结果表明,携带至少一个 基因 rs187115 位点 G 等位基因的个体患 HCC 的风险高于 AA 基因型携带者 ( = 0.007,比值比 (OR) = 1.429,95%置信区间 (CI):1.102-1.854)。同样,携带至少一个 基因 rs3821204 位点 C 等位基因的个体患 HCC 的风险高于 GG 基因型携带者 ( ≤ 0.001,OR = 1.647,95% CI:1.296-2.093)。对 3 个位点的单体型分析表明,rs187115、rs1929992 和 rs3821204 与 HCC 风险相关,在我国某些人群中可能成为 HCC 的有用遗传标志物。

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