Author:
Wen Zhenyu,Li Yingqi,Zhao Zhengping,Li Rongkang,Li Xinji,Lu Chong,Sun Chen,Chen Wenkang,Ge Zhenjian,Ni Liangchao,Lai Yongqing
Abstract
Abstract
Background
Although non-invasive radiological techniques are widely applied in kidney renal clear cell carcinoma (KIRC) diagnosis, more than 50% of KIRCs are detected incidentally during the diagnostic procedures to identify renal cell carcinoma (RCC). Thus, sensitive and accurate KIRC diagnostic methods are required. Therefore, in this study, we aimed to identify KIRC-associated microRNAs (miRNAs).
Methods
This three-phase study included 224 participants (112 each of patients with KIRC and healthy controls (NCs)). RT-qPCR was used to evaluate miRNA expression in KIRC and NC samples. Receiver operating characteristic (ROC) curves and the area under the ROC curve (AUC) were used to predict the usefulness of serum miRNAs in KIRC diagnosis. In addition, we performed survival and bioinformatics analyses.
Results
We found that miR-1-3p, miR-129-5p, miR-146b-5p, miR-187-3p, and miR-200a-3p were significantly differentially expressed in patients with KIRC. A panel consisting of three miRNAs (miR-1-3p, miR-129-5p, and miR-146b-5p) had an AUC of 0.895, ranging from 0.848 to 0.942. In addition, using the GEPIA database, we found that the miRNAs were associated with CREB5. According to the survival analysis, miR-146b-5p overexpression was indicative of a poorer prognosis in patients with KIRC.
Conclusions
The identified three-miRNA panel could serve as a non-invasive indicator for KIRC and CREB5 as a potential target gene for KIRC treatment.
Funder
Clinical Research Project of Peking University Shenzhen Hospital
Science and Technology Development Fund Project of Shenzhen
the Scientific Research Projects of Medical and Health Institutions of Longhua District,.Shenzhen
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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