Exosomal miR-1290 and miR-375 as Prognostic Markers in Castration-resistant Prostate Cancer

被引:531
|
作者
Huang, Xiaoyi [1 ,2 ,3 ]
Yuan, Tiezheng [1 ,2 ]
Liang, Meihua [4 ]
Du, Meijun [1 ,2 ]
Xia, Shu [1 ,2 ,5 ]
Dittmar, Rachel [1 ,2 ]
Wang, Dian [6 ]
See, William [7 ]
Costello, Brian A. [8 ]
Quevedo, Fernando [8 ]
Tan, Winston [9 ]
Nandy, Debashis [8 ]
Bevan, Graham H. [10 ]
Longenbach, Sherri [8 ]
Sun, Zhifu [11 ]
Lu, Yan [12 ]
Wang, Tao [13 ]
Thibodeau, Stephen N. [14 ]
Boardman, Lisa [8 ]
Kohli, Manish [8 ]
Wang, Liang [1 ,2 ]
机构
[1] Med Coll Wisconsin, Dept Pathol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Ctr Canc, Milwaukee, WI 53226 USA
[3] Harbin Med Univ, Affiliated Hosp 3, Biotherapy Ctr, Harbin, Peoples R China
[4] Harbin Med Univ, Affiliated Hosp 2, Dept Endocrinol, Harbin, Peoples R China
[5] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Oncol, Wuhan 430074, Peoples R China
[6] Med Coll Wisconsin, Dept Radiat Oncol, Milwaukee, WI 53226 USA
[7] Med Coll Wisconsin, Dept Urol, Milwaukee, WI 53226 USA
[8] Mayo Clin, Dept Oncol, Rochester, MN USA
[9] Mayo Clin, Dept Oncol, Jacksonville, FL 32224 USA
[10] Univ Rochester, Med Ctr, Rochester, NY 14642 USA
[11] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA
[12] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
[13] Med Coll Wisconsin, Div Biostat, Milwaukee, WI 53226 USA
[14] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
Exosome; microRNA; Extracellular RNA; RNA sequencing; Prostate cancer; Biomarker; Prognosis; Survival; CELL CARCINOMA; GENES; BIOMARKERS; SURVIVAL; PLASMA; SERUM; RNA;
D O I
10.1016/j.eururo.2014.07.035
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
1002 ; 100201 ;
摘要
Background: Extracellular microRNAs (miRNAs) embedded in circulating exosomes may serves as prognostic biomarkers in cancer. Objective: To identify and evaluate plasma exosomal miRNAs for prognosis in castration-resistant prostate cancer (CRPC). Design, setting, and participants: RNA sequencing was performed to identify candidate exosomal miRNAs associated with overall survival in a screening cohort of 23 CRPC patients. Candidate miRNAs were further evaluated for prognosis using quantitative real-time polymerase chain reaction in a follow-up cohort of 100 CRPC patients. Outcome measurements and statistical analysis: Cox regression and Kaplan-Meier survival analyses were used to evaluate survival association using candidate miRNAs along with clinical prognostic factors. Results and limitations: RNA sequencing in screening cohort generated approximately 6.80 million mappable reads per patient. Of those with normalized read counts >= 5, 43% were mapped to miRNAs for a total of 375 known and 57 novel miRNAs. Cox regression analysis identified an association of miR-1290, -1246, and -375 with overall survival (false discover rate < 0.05). Of those, higher levels of miR-1290 and -375 were significantly associated with poor overall survival (p < 0.004) in the follow-up cohort. Incorporation of miR-1290/-375 into putative clinical prognostic factors-based models in CRPC stage significantly improved predictive performance with a time-dependent area under the curve increase from 0.66 to 0.73 (p = 6.57 x 10 (6)). Conclusions: Plasma exosomal miR-1290 and miR-375 are promising prognostic biomarkers for CRPC patients. Prospective validation is needed for further evaluation of these candidate miRNAs. Patient summary: In this study, we evaluated whether small RNAs circulating in blood could be used to predict clinical outcomes in late-stage prostate cancer patients. We identified two blood-based small RNAs whose levels showed significant association with survival. Our results warrant further investigation because the noninvasive blood-based test has great potential in the management of late-stage prostate cancer. (C) 2014 European Association of Urology. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
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