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原发性微小RNA-34b/c rs4938723多态性与肝细胞癌风险相关:一项中国人群的病例对照研究

pri-miR-34b/c rs4938723 polymorphism is associated with hepatocellular carcinoma risk: a case-control study in a Chinese population.

作者信息

Liu Chun-Jia, Ma Xue-Wei, Zhang Xue-Jun, Shen Shi-Qiang

机构信息

Department of General Surgery, The People's Hospital of Wuhan University Wuhan 430060, China.

Chengdu University of Traditional Chinese MedicineChengdu 610000, China; Department of Integrated TCM & Western Medicine, Inner Mongolia People's HospitalHohhot 010017, China.

出版信息

Int J Mol Epidemiol Genet. 2017 Feb 15;8(1):1-7. eCollection 2017.

Abstract

Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide. miR-34 induces changes of its downstream genes, and plays a key role in altering the apoptotic cycle and pathways of downstream cells, and finally influences the development of cancer. We assessed the relationship of the rs4938723 polymorphism with hepatocellular carcinoma risk in a Chinese population. During the period of January 2014 and December 2015, a total of 164 HCC patients and 305 healthy controls were recruited from the Inner Mongolia People's Hospital. Genotyping of the pri-miR-34b/c rs4938723 was determined using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Using χ test, we observed that HCC patients were likely to have a habit of alcohol consumption (χ = 10.24, P = 0.001) and infect with HBV or HCV (χ = 128.17, P < 0.001). In co-dominant model, the CC genotype of rs4938723 had a significant higher risk of HCC as compared with the TT genotype, and the corresponding adjusted OR (95% CI) was 4.14 (1.91-9.75). In dominant model, we observed that the TC+CC genotype were associated with an increased risk of HCC in comparison to the TT genotype (OR = 1.67, 95% CI = 1.17-2.55). In recessive model, the CC genotype was correlated with an elevated risk of HCC when compared with the TT+TC genotype (OR = 3.46, 95% CI = 1.62-8.54). The rs4938723 polymorphism was associated with a higher risk of HCC in the Chinese population examined. Further large-scale and multi-center studies are required to confirm these results.

摘要

肝细胞癌(HCC)是全球最常见的癌症之一。miR-34可诱导其下游基因发生变化,并在改变下游细胞的凋亡周期和途径中起关键作用,最终影响癌症的发展。我们评估了中国人群中rs4938723多态性与肝细胞癌风险的关系。在2014年1月至2015年12月期间,从内蒙古自治区人民医院招募了164例HCC患者和305例健康对照。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对pri-miR-34b/c rs4938723进行基因分型。通过χ检验,我们观察到HCC患者可能有饮酒习惯(χ=10.24,P=0.001),并且感染乙肝病毒或丙肝病毒(χ=128.17,P<0.001)。在共显性模型中,rs4938723的CC基因型与TT基因型相比,HCC风险显著更高,相应的校正比值比(95%可信区间)为4.14(1.91-9.75)。在显性模型中,我们观察到与TT基因型相比,TC+CC基因型与HCC风险增加相关(比值比=1.67,95%可信区间=1.17-2.55)。在隐性模型中,与TT+TC基因型相比,CC基因型与HCC风险升高相关(比值比=3.46,95%可信区间=1.62-8.54)。在所研究的中国人群中,rs4938723多态性与较高的HCC风险相关。需要进一步进行大规模多中心研究来证实这些结果。

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