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miR-627中rs2620381多态性与胃癌的关联

Association of rs2620381 polymorphism in miR-627 and gastric cancer.

作者信息

Raad M, Salehi Z, Habibzaadeh Baalsini M, Mashayekhi F, Saeidi Saedi H

机构信息

Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.

Department of Radiation Oncology, Cancer Research Center, Guilan University of Medical Sciences (GUMS), Rasht, Iran.

出版信息

Br J Biomed Sci. 2020 Apr;77(2):76-80. doi: 10.1080/09674845.2019.1692762. Epub 2020 Jan 27.

Abstract

: Gastric cancer is a complicated malignancy whose aetiology is not well characterized. Single nucleotide polymorphisms (SNPs), some located within microRNA genes, are linked with gastric cancer. We hypothesized a link between SNP rs2620381 (A > C) in miR-627 and gastric cancer.: We recruited 280 healthy controls and 240 gastric cancer patients. Genotyping was conducted by allele-specific polymerase chain reaction. In addition, analyses were carried out via databases and web tools including miRBase, dbSNP, RNAfold, MiRNASNP V2.0, miRWalk V2.0, miRTarBase, and miRmap.: Any C genotype in rs2620381 was linked to gastric cancer: CC vs. AA: OR/95% CI 2.67 (1.17-6.09), p = 0.01, CC+AC vs. AA: OR/95% CI 1.66 (1.12-2.46), p = 0.01, CC vs. AC+AA: OR/95% CI 2.44 (1.07-5.54), p = 0.03. The minor allele C of miR-627 was linked with gastric cancer compared with A allele (OR/95%CI 1.88 (1.30-2.73), p = 0.0008). There were no links between age, sex, tumour type, distant metastasis, and tumour stages and the miR-627 polymorphism in gastric cancer patients.: Presence of the C SNP in miR-627 rs2620381 in linked with gastric cancer, and may be important in pathogenesis.

摘要

胃癌是一种复杂的恶性肿瘤,其病因尚未完全明确。单核苷酸多态性(SNP),其中一些位于微小RNA基因内,与胃癌有关。我们推测微小RNA-627中的SNP rs2620381(A>C)与胃癌之间存在联系。

我们招募了280名健康对照者和240名胃癌患者。通过等位基因特异性聚合酶链反应进行基因分型。此外,还通过包括miRBase、dbSNP、RNAfold、MiRNASNP V2.0、miRWalk V2.0、miRTarBase和miRmap在内的数据库和网络工具进行了分析。

rs2620381中的任何C基因型都与胃癌有关:CC与AA相比:比值比/95%置信区间为2.67(1.17-6.09),p=0.01;CC+AC与AA相比:比值比/95%置信区间为1.66(1.12-2.46),p=0.01;CC与AC+AA相比:比值比/95%置信区间为2.44(1.07-5.54),p=0.03。与A等位基因相比,微小RNA-627的次要等位基因C与胃癌有关(比值比/95%置信区间为1.88(1.30-2.73),p=0.0008)。在胃癌患者中,年龄、性别、肿瘤类型、远处转移和肿瘤分期与微小RNA-627多态性之间没有关联。

微小RNA-627 rs2620381中C SNP 的存在与胃癌有关,可能在发病机制中起重要作用。

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