Circulating exosomal noncoding RNAs as prognostic biomarkers in human hepatocellular carcinoma

外体 微泡 肝细胞癌 小RNA 肿瘤进展 比例危险模型 生物标志物 医学 转移 癌症研究 生存分析 癌症 肿瘤科 内科学 生物 基因 生物化学
作者
Yu Rim Lee,Gyeonghwa Kim,Won Young Tak,Se Young Jang,Young Oh Kweon,Jung Gil Park,Hye Won Lee,Young Seok Han,Jae Min Chun,Soo Young Park,Keun Hur
出处
期刊:International Journal of Cancer [Wiley]
卷期号:144 (6): 1444-1452 被引量:223
标识
DOI:10.1002/ijc.31931
摘要

Exosomal noncoding RNAs (ncRNAs) have unique expression profiles reflecting the characteristics of a tumor, and their role in tumor progression and metastasis is emerging. However, the significance of circulating exosomal ncRNAs in the prognosis of hepatocellular carcinoma (HCC) remains to be elucidated. We therefore determined the prognostic significance of circulating exosomal ncRNAs (miRNA-21 and lncRNA-ATB) for human HCC. This prospective study enrolled 79 HCC patients between October 2014 and September 2015. Exosomes were extracted from serum samples using the ExoQuick Exosome Precipitation Solution. To validate the isolation of the exosomes from serum, immunoblotting for exosome markers and characterization of nanoparticle using NanoSight were performed. NcRNAs were isolated from exosomes using the miRNeasy serum/plasma micro kit. Both circulating exosomal miRNA-21 and lncRNA-ATB were related to TNM stage and other prognostic factors, including the T stage and portal vein thrombosis. Multivariate analysis using the Cox regression test identified that both higher miRNA-21 and higher lncRNA-ATB were independent predictors of mortality and disease progression, along with larger tumor size and higher C-reactive protein (all p < 0.05). The overall survival and progression-free survival were significantly lower in patients with higher circulating levels of exosomal miRNA-21 (≥0.09) and lncRNA-ATB (≥0.0016) (log-rank test: p < 0.05). In conclusion, our study has provided strong evidence that circulating exosomal ncRNAs (miRNA-21 and lncRNA-ATB) are novel prognostic markers and therapeutic targets for HCC.
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