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Association between genetic variant in hsa-miR-146a gene and prostate cancer progression: evidence from Serbian population

机译:hsa-miR-146a基因遗传变异与前列腺癌进展之间的关联:来自塞尔维亚人口的证据

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Purpose: Two previous studies of association between rs2910164 in miR-146a gene and prostate cancer (PCa) risk have provided opposing results. Furthermore, no evidence of association of this SNP with standard prognostic parameters of PCa progression was obtained in mentioned studies. The main aim of this study was to evaluate the possible association between PCa onset and progression to a more aggressive form, since it has not been assessed in a population of European descent.Methods: In this study, 286 samples of peripheral blood were obtained from patients with PCa, while the control group comprised 199 volunteers derived from general population who gave samples of buccal swabs. For individuals diagnosed with PCa clinicopathological characteristics including serum prostate-specific antigen level at diagnosis, Gleason score (GS), and clinical stage were determined. Genotyping of rs2910164 was performed using Taqman?SNP Genotyping Assay. Analysis of SNP association was done using PLINK and SNPStats software.Results: rs2910164 showed no association with PCa risk. Nevertheless, heterozygous genotype was found to be associated with higher GS, as well as with the presence of distant metastases. rs2910164 was also shown to be associated with cancer aggressiveness (p = 0.0067; ORGC = 2.22, 95 %CI 1.24–3.97; ORCC = 0.47, 95 %CI 0.13–1.68).Conclusions: Our results show no evidence of association between rs2910164 and PCa risk in Serbian population. Conversely, this variant was found to be associated with PCa aggressiveness.
机译:目的:先前两项关于miR-146a基因中rs2910164与前列腺癌(PCa)风险之间关联的研究提供了相反的结果。此外,在上述研究中未获得该SNP与PCa进展的标准预后参数相关的证据。这项研究的主要目的是评估PCa发作与进展为更具侵略性的形式之间的可能联系,因为尚未在欧洲血统的人群中对其进行评估。方法:在这项研究中,获得了286份外周血样本患有PCa的患者,而对照组包括199名来自普通人群的志愿者,他们提供了口腔拭子样本。对于诊断为PCa临床病理特征的个体,包括诊断时血清前列腺特异性抗原水平,格里森评分(GS)和临床阶段。使用Taqman?SNP基因分型分析法对rs2910164进行基因分型。使用PLINK和SNPStats软件对SNP关联进行分析。结果:rs2910164显示与PCa风险无关联。然而,发现杂合基因型与较高的GS以及远处转移相关。 rs2910164也显示出与癌症的侵袭性相关(p = 0.0067; ORGC = 2.22,95%CI 1.24–3.97; ORCC = 0.47,95%CI 0.13–1.68)。结论:我们的结果表明,rs2910164与塞尔维亚人口的PCa风险。相反,发现该变体与PCa的侵袭性有关。

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