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Low levels of circulating microRNA-26a/29a as poor prognostic markers in patients with hepatocellular carcinoma who underwent curative treatment.

肿瘤科 生物标志物 小RNA 肝硬化
作者
Hyo Jung Cho,Soon Sun Kim,Ji Sun Nam,Jai Keun Kim,Jei Hee Lee,Bohyun Kim,Hee-Jung Wang,Bong-Wan Kim,J. H. Lee,Dae Yong Kang,Jihyun Kim,Yang Min Jae,Jae Chul Hwang,Sung Jae Shin,Kee Myung Lee,Sung Won Cho,Jae Youn Cheong
出处
期刊:Clinics and Research in Hepatology and Gastroenterology [Elsevier BV]
卷期号:41 (2): 181-189 被引量:30
标识
DOI:10.1016/j.clinre.2016.09.011
摘要

Summary Background/aims We evaluated the prognostic implication of circulating microRNA (miR)-21, miR-26a, and miR-29a in hepatocellular carcinoma (HCC) patients who underwent curative treatment. Methods The study included 120 hepatitis B virus-related HCC patients who underwent hepatic resection ( n  = 63) or radiofrequency ablation ( n  = 57). MiR-21, miR-26a, and miR-29a expression levels in pretreatment plasma and several clinical variables were analyzed to identify prognostic bio-markers. Results Old age, low albumin level, low platelet count, advanced tumor stage (modified Union for International Cancer Control stages III, IV), low miR-26a (hazard ratio [HR] = 1.72; 95% confidence interval [CI] = 1.04–2.83; P  = 0.035), and low miR-29a (HR = 1.75; 95% CI = 1.04–2.94; P  = 0.035) were identified as independent risk factors for predicting poor disease-free survival. Low miR-21, miR-26a, and miR-29a were associated with poor liver transplantation (LT)-free survival in the univariate analysis. Multivariate Cox regression analysis showed that low miR-26a (HR = 3.41; 95% CI = 1.32–8.82; P  = 0.011) and low miR-29a (HR = 2.75; 95% CI = 1.10–6.85; P  = 0.030), low platelet count, and advanced tumor stage were significantly associated with poor LT-free survival. Remarkable correlation was found between miR-26a and miR-29a (Spearman's rho = 0.734, P Conclusion Pretreatment levels of circulating miR-26a and miR-29a are independent prognostic markers for poor disease-free survival and LT-free survival in hepatitis B virus-related HCC patients.
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