Exosomal MicroRNAs Are Diagnostic Biomarkers and Can Mediate Cell-Cell Communication in Renal Cell Carcinoma

被引:116
作者
Butz, Henriett [1 ,2 ,3 ]
Nofech-Mozes, Roy [1 ,2 ]
Ding, Qiang [1 ,2 ]
Khella, Heba W. Z. [1 ,2 ]
Szabo, Peter M. [4 ]
Jewett, Michael [5 ]
Finelli, Antonio [5 ]
Lee, Jason [6 ]
Ordon, Michael [6 ]
Stewart, Robert [6 ]
Krylov, Sergey [7 ,8 ]
Yousef, George M. [1 ,2 ,3 ]
机构
[1] St Michaels Hosp, Dept Lab Med, 30 Bond St, Toronto, ON M5B 1W8, Canada
[2] St Michaels Hosp, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada
[3] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[4] NCI, Biometr Res Branch, Div Canc Treatment & Diag, NIH, Bethesda, MD 20892 USA
[5] Princess Margaret Hosp, Dept Surg, Toronto, ON, Canada
[6] St Michaels Hosp, Dept Surg, Toronto, ON, Canada
[7] York Univ, Dept Chem, Toronto, ON, Canada
[8] York Univ, Ctr Res Biomol Interact, Toronto, ON, Canada
关键词
Exosomes; miRNAs; Noninvasive biomarker; Renal cell carcinoma; Urine; Cell-cell communication;
D O I
10.1016/j.euf.2015.11.006
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Background: Apart from an invasive biopsy, currently no tools are available to confirm the diagnosis of clear cell renal cell carcinoma (ccRCC); this resulted in approximately 30% of patients being diagnosed with metastatic disease. Objective: To determine whether urinary microRNAs (miRNAs) can serve as biomarkers to confirm the diagnosis of ccRCC. Design, setting, and participants: Global miRNA expression was assessed in 28 preoperative urine samples from patients with ccRCC and 18 healthy participants. The independent validation set consisted of 81 ccRCC patients, 24 patients with benign lesions, and 33 healthy participants. We extracted both cell-free and exosomal RNA for miRNA expression analysis using miRNA-specific polymerase chain reaction assays. We also investigated exosomal miRNA secretion in cell line models and performed exosome transfer between RCC and endothelial cell types. Outcome measurements and statistical analysis: Receiver operating characteristic analysis was applied to identify the discrimination power of miRNAs. Results and limitations: Overall, miR-126-3p combined with miR-449a or with miR-34b-5p could significantly distinguish ccRCC patients from healthy participants (miR-126-3p-miR-449a: area under the curve [AUC]: 0.84; 95% confidence interval [CI], 0.7620-0.9151; p < 0.001; miR-126-3p-miR-34b-5p: AUC: 0.79; 95% CI, 0.7013-0.8815; p < 0.001). The combination of miR-126-3p and miR-34b-5p was also able to distinguish small renal masses (pT1a, <= 4 cm) from healthy controls (AUC: 0.79; 95% CI, 0.6848-0.8980; p < 0.001). Using miR-126-3p and miR-486-5p in combination, we were able to differentiate between benign lesions and ccRCC (AUC: 0.85; 95% CI, 0.7295-0.9615; p < 0.01). The expression of a number of miRNAs returned to a level comparable with health after surgery. Kidney cancer cell lines were found to secrete exosomal miR-126-3p, miR-17-5p, miR-21-3p, and miR-25-3p, and these miRNAs were found to be internalized by other cell types. Conclusions: We identified exosomal miRNAs as potential noninvasive diagnostic urinary biomarkers for ccRCC and provided evidence that miRNAs are secreted by the tumor and can function as a tool for intercellular communication. Patient summary: We identified urinary microRNAs that can serve as diagnostic biomarkers for clear cell renal cell carcinoma. (C) 2015 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:210 / 218
页数:9
相关论文
共 30 条
[1]
From bench to bedside: current and future applications of molecular profiling in renal cell carcinoma [J].
Arsanious, Androu ;
Bjarnason, Georg A. ;
Yousef, George M. .
MOLECULAR CANCER, 2009, 8
[2]
MicroRNA-449a acts as a tumor suppressor in human bladder cancer through the regulation of pocket proteins [J].
Chen, Hong ;
Lin, Yi-Wei ;
Mao, Ye-Qing ;
Wu, Jian ;
Liu, Yun-Fu ;
Zheng, Xiang-Yi ;
Xie, Li-Ping .
CANCER LETTERS, 2012, 320 (01) :40-47
[3]
MicroRNA profile indicates downregulation of the TGFβ pathway in sporadic non-functioning pituitary adenomas [J].
Henriett Butz ;
Istvan Liko ;
Sandor Czirjak ;
Peter Igaz ;
Marta Korbonits ;
Karoly Racz ;
Attila Patocs .
PITUITARY, 2011, 14 (02) :112-124
[4]
Extracellular MicroRNAs in Urologic Malignancies: Chances and Challenges [J].
Huang, Xiaoyi ;
Liang, Meihua ;
Dittmar, Rachel ;
Wang, Liang .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (07) :14785-14799
[5]
Renal tumor-derived exosomes inhibit hepaCAM expression of renal carcinoma cells in a p-AKT-dependent manner [J].
Jiang, X. L. ;
Zhang, Y. ;
Tan, B. ;
Luo, C. L. ;
Wu, X. H. .
NEOPLASMA, 2014, 61 (04) :416-423
[6]
Identification of a MicroRNA Panel for Clear-cell Kidney Cancer [J].
Juan, David ;
Alexe, Gabriela ;
Antes, Travis ;
Liu, Huiqing ;
Madabhushi, Anant ;
Delisi, Charles ;
Ganesan, Shridhar ;
Bhanot, Gyan ;
Liou, Louis S. .
UROLOGY, 2010, 75 (04) :835-841
[7]
MicroRNA profiling of clear cell renal cell cancer identifies a robust signature to define renal malignancy [J].
Jung, Monika ;
Mollenkopf, Hans-Joachim ;
Grimm, Christina ;
Wagner, Ina ;
Albrecht, Marco ;
Waller, Tobias ;
Pilarsky, Christian ;
Johannsen, Manfred ;
Stephan, Carsten ;
Lehrach, Hans ;
Nietfeld, Wilfried ;
Rudel, Thomas ;
Jung, Klaus ;
Kristiansen, Glen .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2009, 13 (9B) :3918-3928
[8]
Exploring the role of miRNAs in renal cell carcinoma progression and metastasis through bioinformatic and experimental analyses [J].
Khella, Heba W. Z. ;
White, Nicole M. A. ;
Faragalla, Hala ;
Gabril, Manal ;
Boazak, Mina ;
Dorian, David ;
Khalil, Bishoy ;
Antonios, Hany ;
Bao, Tian Tian ;
Pasic, Maria D. ;
Honey, R. John ;
Stewart, Robert ;
Pace, Kenneth T. ;
Bjarnason, Georg A. ;
Jewett, Michael A. S. ;
Yousef, George M. .
TUMOR BIOLOGY, 2012, 33 (01) :131-140
[9]
Kurban G, 2013, ARCH ESP UROL, V66, P505
[10]
Microvesicle-mediated Transfer of MicroRNA-150 from Monocytes to Endothelial Cells Promotes Angiogenesis [J].
Li, Jing ;
Zhang, Yujing ;
Liu, Yuchen ;
Dai, Xin ;
Li, Wenyang ;
Cai, Xing ;
Yin, Yuan ;
Wang, Qiang ;
Xue, Yunxing ;
Wang, Cheng ;
Li, Dameng ;
Hou, Dongxia ;
Jiang, Xiaohong ;
Zhang, Junfeng ;
Zen, Ke ;
Chen, Xi ;
Zhang, Chen-Yu .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (32) :23586-23596