miR-566 functions as an oncogene and a potential biomarker for prognosis in renal cell carcinoma

被引:19
作者
Pan, Xiang [1 ,2 ,4 ]
Quan, Jing [1 ,2 ,4 ]
Li, Zuwei [1 ,3 ,4 ]
Zhao, Liwen [1 ,2 ,4 ]
Zhou, Liang [1 ,4 ,5 ]
Xu, Jinling [1 ]
Xu, Weijie [1 ]
Guan, Xin [1 ]
Li, Hang [1 ]
Yang, Shangqi [1 ]
Gui, Yaoting [4 ]
Lai, Yongqing [1 ,4 ]
机构
[1] Peking Univ, Dept Urol, Shenzhen Hosp, 1120 Lianhua Rd, Shenzhen 518036, Guangdong, Peoples R China
[2] Anhui Med Univ, Dept Urol, Hefei 230032, Anhui, Peoples R China
[3] Shantou Univ, Dept Urol, Coll Med, Shantou 515041, Guangdong, Peoples R China
[4] Peking Univ, Shenzhen Hosp, Guangdong & Shenzhen Key Lab Male Reprod Med & Ge, Inst Urol Shenzhen PKU HKUST Med Ctr, Shenzhen 518036, Guangdong, Peoples R China
[5] Guangzhou Med Univ, Dept Urol, Guangzhou 511436, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNAs; miR-566; Renal cell carcinoma; Oncogene; Prognosis biomarker; TUMOR-SUPPRESSOR; MICRORNAS; APOPTOSIS; CANCER;
D O I
10.1016/j.biopha.2018.03.072
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Renal cell carcinoma (RCC), a heterogeneous type of cancer originating from the nephron, occupies approximately 3.9% of new carcinomas, with an increasing incidence in the past two decades. The most common subtype of renal cell carcinoma is clear cell RCC (ccRCC). Though surgery and other treatments are applied to RCC, it has the highest recurrence rate and mortality rate among the genitourinary cancers. As the study progressed, miRNAs are found to be the biomarkers for tumor diagnosis, prognosis and the targets for tumor management. Methods: In present study, RT-qPCR, wound scratch assay, cell proliferation assay, transwell assay and flow cytometry assay were performed to ascertain miR-566 expression level and its proliferation, migration and apoptosis in RCC. Moreover, we analyzed the relation between miR-566 expression and clinicopathological variables or overall survival from the 42 formalin-fixed paraffin-embedded (FFPE) renal cancer samples. We further evaluate prognostic values of miR-566 expression. Results: miR-566 is up-regulated in RCC tissue samples and renal carcinoma cell lines. miR-566 promotes cell proliferation, mobility and inhibits cell apoptosis in 786-O and ACHN cell lines. Cox proportional hazard regression analysis indicates that low expression of miR-566 patients have a remarkable longer overall survival in the univariate and multivariate analysis. The Kaplan-Meier survival curves show that the low expression of miR-566 patients have a remarkable longer overall survival. Conclusions: The results of the current study demonstrate that oncogene miR-566 is a potential biomarker not only for diagnosis but also for prognosis for RCC.
引用
收藏
页码:718 / 727
页数:10
相关论文
共 26 条
[1]  
[Anonymous], ONCOGENE
[2]   Treatment of renal cell carcinoma: Current status and future directions [J].
Barata, Pedro C. ;
Rini, Brian I. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2017, 67 (06) :507-524
[3]   Landmarks in the diagnosis and treatment of renal cell carcinoma [J].
Bhatt, Jaimin R. ;
Finelli, Antonio .
NATURE REVIEWS UROLOGY, 2014, 11 (09) :517-525
[4]   Renal cell carcinoma [J].
Cairns, Paul .
CANCER BIOMARKERS, 2011, 9 (1-6) :461-473
[5]   MicroRNA in Prostate, Bladder, and Kidney Cancer: A Systematic Review [J].
Catto, James W. F. ;
Alcaraz, Antonio ;
Bjartell, Anders S. ;
White, Ralph De Vere ;
Evans, Christopher P. ;
Fussel, Susanne ;
Hamdy, Freddie C. ;
Kallioniemi, Olli ;
Mengual, Lourdes ;
Schlomm, Thorsten ;
Visakorpi, Tapio .
EUROPEAN UROLOGY, 2011, 59 (05) :671-681
[6]   Multilevel Genomics-Based Taxonomy of Renal Cell Carcinoma [J].
Chen, Fengju ;
Zhang, Yiqun ;
Senbabaoglu, Yasin ;
Ciriello, Giovanni ;
Yang, Lixing ;
Reznik, Ed ;
Shuch, Brian ;
Micevic, Goran ;
De Velasco, Guillermo ;
Shinbrot, Eve ;
Noble, Michael S. ;
Lu, Yiling ;
Covington, Kyle R. ;
Xi, Liu ;
Drummond, Jennifer A. ;
Muzny, Donna ;
Kang, Hyojin ;
Lee, Junehawk ;
Tamboli, Pheroze ;
Reuter, Victor ;
Shelley, Carl Simon ;
Kaipparettu, Benny A. ;
Bottaro, Donald P. ;
Godwin, Andrew K. ;
Gibbs, Richard A. ;
Getz, Gad ;
Kucherlapati, Raju ;
Park, Peter J. ;
Sander, Chris ;
Henske, Elizabeth P. ;
Zhou, Jane H. ;
Kwiatkowski, David J. ;
Ho, Thai H. ;
Choueiri, Toni K. ;
Hsieh, James J. ;
Akbani, Rehan ;
Mills, Gordon B. ;
Hakimi, A. Ari ;
Wheeler, David A. ;
Creighton, Chad J. .
CELL REPORTS, 2016, 14 (10) :2476-2489
[7]   MicroRNA Profiles Discriminate among Colon Cancer Metastasis [J].
Drusco, Alessandra ;
Nuovo, Gerard J. ;
Zanesi, Nicola ;
Di Leva, Gianpiero ;
Pichiorri, Flavia ;
Volinia, Stefano ;
Fernandez, Cecilia ;
Antenucci, Anna ;
Costinean, Stefan ;
Bottoni, Arianna ;
Rosito, Immacolata A. ;
Liu, Chang-Gong ;
Burch, Aaron ;
Acunzo, Mario ;
Pekarsky, Yuri ;
Alder, Hansjuerg ;
Ciardi, Antonio ;
Croce, Carlo M. .
PLOS ONE, 2014, 9 (06)
[8]   The role of microRNAs in bladder cancer [J].
Enokida, Hideki ;
Yoshino, Hirofumi ;
Matsushita, Ryosuke ;
Nakagawa, Masayuki .
INVESTIGATIVE AND CLINICAL UROLOGY, 2016, 57 :S60-S76
[9]   MiRNA-200a induce cell apoptosis in renal cell carcinoma by directly targeting SIRT1 [J].
Fu, Hao ;
Song, Wenke ;
Chen, Xuancai ;
Guo, Tao ;
Duan, Bin ;
Wang, Xinxi ;
Tang, Yachun ;
Huang, Liang ;
Zhang, Chi .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2018, 437 (1-2) :143-152
[10]  
Homami Amene, 2016, Med J Islam Repub Iran, V30, P475