Department of Laboratory Medicine, Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital, and Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
J Urol. 2011 Sep;186(3):1077-83. doi: 10.1016/j.juro.2011.04.110. Epub 2011 Jul 23.
Renal cell carcinoma is the most common neoplasm of the adult kidney. Currently to our knowledge there are no biomarkers for diagnostic, prognostic or predictive applications for renal cell carcinoma. miRNAs are nonprotein coding RNAs that negatively regulate gene expression and are potential biomarkers for cancer.
We analyzed 70 matched pairs of clear cell renal cell carcinoma and normal kidney tissues from the same patients by microarray analysis and validated our results by quantitative real-time polymerase chain reaction. We also performed extensive bioinformatic analysis to explore the role and regulation of miRNAs in clear cell renal cell carcinoma.
We identified 166 miRNAs that were significantly dysregulated in clear cell renal cell carcinoma, including miR-122, miR-155 and miR-210, which had the highest over expression, and miR-200c, miR-335 and miR-218, which were most down-regulated. Analysis of previously reported miRNAs dysregulated in RCC showed overall agreement in the direction of dysregulation. Extensive target prediction analysis revealed that many miRNAs were predicted to target genes involved in renal cell carcinoma pathogenesis. In renal cell carcinoma miRNA dysregulation can be attributed in part to chromosomal aberrations, co-regulation of miRNA clusters and co-expression with host genes. We also performed a preliminary analysis showing that miR-155 expression correlated with clear cell renal cell carcinoma size. This finding must be validated in a larger independent cohort.
Analysis showed that miRNAs are dysregulated in clear cell renal cell carcinoma and may contribute to kidney cancer pathogenesis by targeting more than 1 key molecule. We identified mechanisms that may contribute to miRNA dysregulation in clear cell renal cell carcinoma. Dysregulated miRNAs represent potential biomarkers for kidney cancer.
肾细胞癌是成人肾脏最常见的肿瘤。目前据我们所知,肾细胞癌没有用于诊断、预后或预测的生物标志物。miRNA 是非编码蛋白的 RNA,可以负调控基因表达,是癌症的潜在生物标志物。
我们通过微阵列分析对 70 对来自同一患者的透明细胞肾细胞癌和正常肾组织进行了分析,并通过定量实时聚合酶链反应验证了我们的结果。我们还进行了广泛的生物信息学分析,以探讨 miRNA 在透明细胞肾细胞癌中的作用和调控。
我们鉴定了 166 个在透明细胞肾细胞癌中显著失调的 miRNA,包括 miR-122、miR-155 和 miR-210,它们的表达水平最高,而 miR-200c、miR-335 和 miR-218 的表达水平最低。对已报道的 RCC 中失调的 miRNA 的分析显示,在失调方向上总体一致。广泛的靶标预测分析表明,许多 miRNA 被预测靶向参与肾细胞癌发病机制的基因。在肾细胞癌中,miRNA 的失调部分归因于染色体异常、miRNA 簇的共同调控以及与宿主基因的共同表达。我们还进行了初步分析,表明 miR-155 的表达与透明细胞肾细胞癌的大小有关。这一发现必须在更大的独立队列中进行验证。
分析表明,miRNA 在透明细胞肾细胞癌中失调,可能通过靶向超过 1 个关键分子来促进肾癌的发病机制。我们确定了可能导致透明细胞肾细胞癌中 miRNA 失调的机制。失调的 miRNA 代表了肾癌的潜在生物标志物。