Nikolić Z, Savić Pavićević D, Vučić N, Cidilko S, Filipović N, Cerović S, Vukotić V, Romac S, Brajušković G
University of Belgrade, Faculty of Biology, Belgrade, Serbia.
Department of Urology, Clinical Centre "dr Dragiša Mišović", Belgrade, Serbia.
Exp Mol Pathol. 2015 Aug;99(1):145-50. doi: 10.1016/j.yexmp.2015.06.009. Epub 2015 Jun 22.
Due to their potentially functional significance, genetic variants within microRNA genes have been recognized as candidates for cancer-related genetic biomarkers. Among the most extensively studied so far are rs3746444, rs11614913 and rs895819. Nevertheless, only few previous studies in Asian population analyzed the association of rs3746444 and rs11614913 with prostate cancer (PCa) risk, while rs895819 was not evaluated in relation to this issue. The aim of this study was to assess the possible association between these genetic variants and PCa risk and progression in Serbian population. 355 samples of peripheral blood were obtained from the patients with PCa and 353 samples from patients with benign prostatic hyperplasia (BPH). 312 volunteers derived from general population who gave samples of buccal swabs were included in the control group. Genotyping of rs3746444, rs11614913 and rs895819 was performed by using PCR-RFLP method, HRM analysis and allele-specific PCR, respectively. Allelic and genotypic associations were evaluated by unconditional linear (for serum PSA level in PCa patients) and logistic regression method with adjustment for age. Minor allele C of rs895819 was found to be associated with the increased risk of developing PCa under dominant (P=0.035; OR=1.38, 95%CI 1.02-1.86) and overdominant (P=0.04; OR=1.37, 95%CI 1.01-1.85) genetic model. Same genetic variant was found to be associated with the clinical stage of localized PCa, as well as with the presence of distant metastases. Allele G of rs3746444 was also shown to be associated with the decreased risk of PCa progression. According to our data, rs3746444 qualifies for a genetic variant potentially associated with PCa aggressiveness in Serbian population. Furthermore, our study provided the first evidence of association between rs895819 and PCa risk, as well as for its genetic association with the presence of distant metastases among PCa patients.
由于其潜在的功能意义,微小RNA基因内的遗传变异已被视为癌症相关遗传生物标志物的候选者。迄今为止研究最广泛的是rs3746444、rs11614913和rs895819。然而,此前在亚洲人群中只有少数研究分析了rs3746444和rs11614913与前列腺癌(PCa)风险的关联,而rs895819在这方面尚未得到评估。本研究的目的是评估这些遗传变异与塞尔维亚人群中PCa风险及进展之间的可能关联。从PCa患者中获取了355份外周血样本,从良性前列腺增生(BPH)患者中获取了353份样本。对照组纳入了312名来自普通人群并提供颊拭子样本的志愿者。分别采用PCR-RFLP方法、高分辨率熔解曲线分析(HRM)和等位基因特异性PCR对rs3746444、rs11614913和rs895819进行基因分型。通过无条件线性回归(针对PCa患者的血清前列腺特异抗原水平)和逻辑回归方法评估等位基因和基因型关联,并对年龄进行校正。发现rs895819的次要等位基因C在显性遗传模型(P = 0.035;OR = 1.38,95%CI 1.02 - 1.86)和超显性遗传模型(P = 0.04;OR = 1.37,95%CI 1.01 - 1.85)下与PCa发病风险增加相关。同一遗传变异被发现与局限性PCa的临床分期以及远处转移的存在相关。rs3746444的等位基因G也显示与PCa进展风险降低相关。根据我们的数据,rs3746444有资格作为可能与塞尔维亚人群中PCa侵袭性相关的遗传变异。此外,我们的研究首次提供了rs895819与PCa风险之间关联的证据,以及其与PCa患者中远处转移存在的遗传关联证据。