人类透明细胞肾细胞癌中 HIF-1α 的表达和基因多态性分析

Daniela Vargová, Zuzana Kolková, Ján Dargaj, Lukáš Briš, J. Ľupták, Zuzana Dankova, S. Fraňová, Jan Svihra, P. Slávik, M. Šutovská
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摘要

导言:透明细胞肾细胞癌(ccRCC)多为偶发诊断,复发率相对较高。VHL/HIF和mTOR通路的改变常见于ccRCC。本研究试图在生化和分子水平上确定潜在的诊断标志物:方法:共招募了 54 名受试者(36 名 ccRCC 患者和 18 名无癌症对照者)。采用酶联免疫吸附法测定肿瘤和健康肾组织中 HIF-1α 的水平。利用实时聚合酶链式反应(real-time PCR)研究了斯洛伐克队列中病理相关通路(VHL/HIF和mTOR)基因中的五个选定SNPs(rs779805、rs11549465、rs2057482、rs2295080和rs701848)与ccRCC风险之间的关联:结果:在肿瘤和健康肾组织之间观察到 HIF-1α 组织水平的显著差异(p < 0.001)。在大多数病例(69%)中,肾脏中的 HIF-1α 水平高于肿瘤。此外,肿瘤中的 HIF-1α 浓度与 CCL3 和 IL-1β 呈显著正相关(p (R2) 0.007 (0.47);p (R2) 0.011 (0.38))。未观察到 HIF-1α 瘤内水平与临床肿瘤特征之间的关系。HIF1A 基因中的 Rs11549465、rs2057482 与肿瘤或正常肾脏中 HIF-1α 的表达均无相关性。所选 SNPs 均未影响 ccRCC 的易感性:结论:要阐明HIF-1α在ccRCC发病机制中的作用以及所选SNPs与该癌症易感性之间的关联,还需要更多的研究。
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Analysis of HIF-1α expression and genetic polymorphisms in human clear cell renal cell carcinoma
Introduction: Clear cell renal cell carcinoma (ccRCC) is mostly diagnosed incidentally and has relatively high recurrence rates. Alterations in VHL/HIF and mTOR pathways are commonly present in ccRCC. The present study attempted to identify potential diagnostic markers at the biochemical and molecular level.Methods: In total, 54 subjects (36 patients with ccRCC and 18 cancer-free controls) were enrolled. ELISA was used to measure the levels of HIF-1α in the tumor and healthy kidney tissue. The association between five selected SNPs (rs779805, rs11549465, rs2057482, rs2295080 and rs701848) located in genes of pathologically relevant pathways (VHL/HIF and mTOR) and the risk of ccRCC in the Slovak cohort was studied using real-time PCR.Results: Significant differences in HIF-1α tissue levels were observed between the tumor and healthy kidney tissue (p < 0.001). In the majority (69%) of cases, the levels of HIF-1α were higher in the kidney than in the tumor. Furthermore, the concentration of HIF-1α in the tumor showed a significant positive correlation with CCL3 and IL-1β (p (R2) 0.007 (0.47); p (R2) 0.011 (0.38). No relationship between intratumoral levels of HIF-1α and clinical tumor characteristics was observed. Rs11549465, rs2057482 in the HIF1A gene did not correlate with the expression of HIF-1α either in the tumor or in the normal kidney. None of the selected SNPs has influenced the susceptibility to ccRCC.Conclusion: More research is neccesary to elucidate the role of HIF-1α in the pathogenesis of ccRCC and the association between selected SNPs and susceptibility to this cancer.
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