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中国汉族人群基因多态性与肝细胞癌风险的病例对照研究

A Case-Control Study of Gene Polymorphisms and the Risk of Hepatocellular Carcinoma in the Chinese Han Population.

作者信息

Chao Xu, Jia Yong, Feng Xuesong, Wang Guoquan, Wang Xiaoping, Shi Hailong, Zhao Fei, Jiang Chao

机构信息

The College of Basic Medicine, Shaanxi University of Chinese Medicine, Xianyang, China.

The Second Affiliated Hospital, Shaanxi University of Chinese Medicine, Xianyang, China.

出版信息

Front Oncol. 2020 Aug 25;10:1450. doi: 10.3389/fonc.2020.01450. eCollection 2020.

Abstract

Adenylyl cyclase type 9 () modulates signal transduction by producing the second messenger cyclic AMP. It has been reported that gene polymorphisms were associated with cancer development. The aim of this study was to investigate whether gene polymorphisms could contribute to the susceptibility of hepatocellular carcinoma (HCC) in the Chinese Han population. In the present study, five single-nucleotide polymorphisms (SNPs) in were genotyped using Agena MassARRAY platform in 876 subjects from China. Logistic regression was used to assess the effects of SNPs on HCC risk. Associations were also evaluated for HCC risk stratified by age and gender. False discovery rate (FDR) was used to correct multiple testing. After adjusting for age and gender, we found a significant relationship between heterozygous genotypes of rs2531995 and HCC risk (OR = 1.34, 95% CI = 1.01-1.77, = 0.045). rs2230742 had a strong relationship with lower risk of HCC in allele ( = 0.006), co-dominant ( = 0.023), dominant ( = 0.010), and additive ( = 0.006) models. Stratified analysis showed that rs879620 increased HCC risk and rs2230742 was associated with lower risk of HCC in the individuals aged 55 or younger, rs2531992 significantly decreased HCC risk in the elder group (age > 55). For women, rs2230742 and rs2230741 were significantly associated with HCC risk in multiple models ( < 0.05). FDR analysis showed that rs2230742 could protect individuals from HCC risk in the allele model (FDR = 0.030). In addition, haplotype analysis indicated that CAA haplotype was a protective factor for HCC (OR = 0.67, 95% CI = 0.50-0.89, = 0.007, FDR = 0.028). Our findings suggest that gene polymorphisms are associated with HCC risk in the Chinese Han population.

摘要

9型腺苷酸环化酶()通过产生第二信使环磷酸腺苷来调节信号转导。据报道,基因多态性与癌症发生有关。本研究的目的是调查基因多态性是否会影响中国汉族人群肝细胞癌(HCC)的易感性。在本研究中,使用Agena MassARRAY平台对来自中国的876名受试者的中的五个单核苷酸多态性(SNP)进行基因分型。采用逻辑回归分析评估SNP对HCC风险的影响。还按年龄和性别对HCC风险分层进行了关联评估。使用错误发现率(FDR)来校正多重检验。在调整年龄和性别后,我们发现rs2531995的杂合基因型与HCC风险之间存在显著关系(OR = 1.34,95% CI = 1.01 - 1.77,= 0.045)。rs2230742在等位基因模型(= 0.006)、共显性模型(= 0.023)、显性模型(= 0.010)和加性模型(= 0.006)中与较低的HCC风险密切相关。分层分析表明,rs879620增加了HCC风险,而rs2230742在年龄55岁及以下的个体中与较低的HCC风险相关,rs2531992在老年组(年龄>55岁)中显著降低了HCC风险。对于女性,rs2230742和rs2230741在多个模型中与HCC风险显著相关(<0.05)。FDR分析表明,rs2230742在等位基因模型中可保护个体免受HCC风险(FDR = 0.030)。此外,单倍型分析表明,CAA单倍型是HCC的保护因素(OR = 0.67,95% CI = 0.50 - 0.89,= 0.007,FDR = 0.028)。我们的研究结果表明,基因多态性与中国汉族人群的HCC风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee22/7477943/e122e183b09f/fonc-10-01450-g0001.jpg

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