Expression of serum miR-221 in human hepatocellular carcinoma and its prognostic significance

被引:236
作者
Li, Jipeng [1 ]
Wang, Yiping [1 ]
Yu, Wanjun [1 ]
Chen, Jun [2 ]
Luo, Jianping [1 ]
机构
[1] Yinzhou Peoples Hosp, Lab Med Ctr, Ningbo 315040, Zhejiang, Peoples R China
[2] Hangzhou Normal Univ, Dept Clin Lab, Affiliated Hosp, Hangzhou 310015, Peoples R China
关键词
microRNA; Serum; HCC; Prognosis; MICRORNA EXPRESSION; CIRCULATING MICRORNAS; CANCER; PCR; TUMOR; PROLIFERATION; BIOMARKERS; INJURY;
D O I
10.1016/j.bbrc.2011.01.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Objective: To investigate whether the serum miR-221 expression correlates with clinicopathologic features and the prognosis of hepatocellular carcinoma (HCC) patients. Methods: Four miRNAs (miR-221, miR-222, miR-21 and miR-224) related to HCC were selected in the present study. Serum miRNA expression was investigated in 46 HCC patients and 20 healthy normal controls by using real-time PCR technique, and then correlations between miR-221 expression and the clinicopathological features and prognosis of HCC patients were evaluated. Results: The four miRNAs were found to be differentially overexpressed in HCC serum samples, and high level of miR-221 expression was correlated with tumor size (P < 0.001), cirrhosis (P = 0.003) and tumor stage (P = 0.016). In addition, Kaplan-Meier survival analysis showed that the overall survival rate of the high miR-221 expression group (27.6%) was significantly lower than that of the low miR-221 expression group (62.3%, P < 0.05). Conclusions: Serum miR-221, upregulated in HCC, can provide predictive significance for prognosis of HCC patients. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:70 / 73
页数:4
相关论文
共 29 条
[1]   Real-time quantification of microRNAs by stem-loop RT-PCR [J].
Chen, CF ;
Ridzon, DA ;
Broomer, AJ ;
Zhou, ZH ;
Lee, DH ;
Nguyen, JT ;
Barbisin, M ;
Xu, NL ;
Mahuvakar, VR ;
Andersen, MR ;
Lao, KQ ;
Livak, KJ ;
Guegler, KJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e179.1-e179.9
[2]   Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases [J].
Chen, Xi ;
Ba, Yi ;
Ma, Lijia ;
Cai, Xing ;
Yin, Yuan ;
Wang, Kehui ;
Guo, Jigang ;
Zhang, Yujing ;
Chen, Jiangning ;
Guo, Xing ;
Li, Qibin ;
Li, Xiaoying ;
Wang, Wenjing ;
Zhang, Yan ;
Wang, Jin ;
Jiang, Xueyuan ;
Xiang, Yang ;
Xu, Chen ;
Zheng, Pingping ;
Zhang, Juanbin ;
Li, Ruiqiang ;
Zhang, Hongjie ;
Shang, Xiaobin ;
Gong, Ting ;
Ning, Guang ;
Wang, Jun ;
Zen, Ke ;
Zhang, Junfeng ;
Zhang, Chen-Yu .
CELL RESEARCH, 2008, 18 (10) :997-1006
[3]   A translational study of circulating cell-free microRNA-1 in acute myocardial infarction [J].
Cheng, Yunhui ;
Tan, Ning ;
Yang, Jian ;
Liu, Xiaojun ;
Cao, Xiaopei ;
He, Pengcheng ;
Dong, Xiaoli ;
Qin, Shanshan ;
Zhang, Chunxiang .
CLINICAL SCIENCE, 2010, 119 (1-2) :87-95
[4]   Hepatocellular carcinoma: Epidemiology and molecular carcinogenesis [J].
El-Serag, Hashem B. ;
Rudolph, Lenhard .
GASTROENTEROLOGY, 2007, 132 (07) :2557-2576
[5]   miR-221 and miR-222 expression affects the proliferation potential of human prostate carcinoma cell lines by targeting p27Kip1* [J].
Galardi, Silvia ;
Mercatelli, Neri ;
Giorda, Ezio ;
Massalini, Simone ;
Frajese, Giovanni Vanni ;
Ciafre, Silvia Anna ;
Farace, Maria Giulia .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (32) :23716-23724
[6]   The role of microRNA genes in papillary thyroid carcinoma [J].
He, HL ;
Jazdzewski, K ;
Li, W ;
Liyanarachchi, S ;
Nagy, R ;
Volinia, S ;
Calin, GA ;
Liu, CG ;
Franssila, K ;
Suster, S ;
Kloos, RT ;
Croce, CM ;
de la Chapelle, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (52) :19075-19080
[7]   Plasma miR-208 as a Biomarker of Myocardial Injury [J].
Ji, Xu ;
Takahashi, Rie ;
Hiura, Yumiko ;
Hirokawa, Go ;
Fukushima, Yasue ;
Iwai, Naoharu .
CLINICAL CHEMISTRY, 2009, 55 (11) :1944-1949
[8]   HEPATIC RESECTION FOR HEPATOCELLULAR-CARCINOMA - AN AUDIT OF 343 PATIENTS [J].
LAI, ECS ;
FAN, ST ;
CHU, KM ;
WONG, J .
ANNALS OF SURGERY, 1995, 221 (03) :291-298
[9]  
Lau H, 1998, CANCER-AM CANCER SOC, V83, P2302, DOI 10.1002/(SICI)1097-0142(19981201)83:11<2302::AID-CNCR9>3.3.CO
[10]  
2-T