Combination of MiR-378 and MiR-210 Serum Levels Enables Sensitive Detection of Renal Cell Carcinoma

被引:73
作者
Fedorko, Michal [1 ,2 ]
Stanik, Michal [3 ]
Iliev, Robert [4 ,5 ]
Redova-Lojova, Martina [5 ]
Machackova, Tana [5 ]
Svoboda, Marek [4 ]
Pacik, Dalibor [1 ,2 ]
Dolezel, Jan [3 ]
Slaby, Ondrej [4 ,5 ]
机构
[1] Univ Hosp Brno, Dept Urol, Brno 62500, Czech Republic
[2] Masaryk Univ, Brno 62500, Czech Republic
[3] Masaryk Mem Canc Inst, Dept Urol Oncol, Brno 65653, Czech Republic
[4] Masaryk Mem Canc Inst, Dept Comprehens Canc Care, Brno 65653, Czech Republic
[5] Masaryk Univ, Cent European Inst Technol, Brno 62500, Czech Republic
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2015年 / 16卷 / 10期
关键词
renal cell carcinoma; microRNA; blood serum; biomarker; COLORECTAL-CANCER; MICRORNAS; BIOMARKERS; PLASMA;
D O I
10.3390/ijms161023382
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Serum microRNAs are emerging as a clinically useful tool for early and non-invasive detection of various cancer types including renal cell carcinoma (RCC). Based on our previous results, we performed the study to analyze circulating serum miR-378 and miR-210 in patients with various histological subtypes of RCC. RNA was purified from blood serum samples of 195 RCC patients and 100 healthy controls. The levels of miR-378 and miR-210 in serum were determined absolutely using quantitative real-time PCR. Pre- and postoperative levels of both microRNAs were compared in 20 RCC patients. Significantly increased serum levels of both miR-378 and miR-210 enabled to clearly distinguish RCC patients and healthy controls with 80% sensitivity and 78% specificity if analyzed in combination (p < 0.0001), and their levels significantly decreased in the time period of three months after radical nephrectomy (p < 0.0001). Increased level of miR-378 positively correlates with disease-free survival (p = 0.036) and clinical stage (p = 0.0476). The analysis of serum miR-378 and miR-210 proved their potential to serve as powerful non-invasive diagnostic and prognostic biomarkers in RCC.
引用
收藏
页码:23382 / 23389
页数:8
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