Down-regulation of microRNA-181b is a potential prognostic marker of non-small cell lung cancer

被引:48
作者
Yang, Junquan [1 ]
Liu, Hongxia [2 ]
Wang, Hongbin [1 ]
Sun, Yuman [2 ]
机构
[1] Peoples Hosp Tangshan City, Dept Radiotherapy & Chemotherapy, Tangshan City, Hebei Province, Peoples R China
[2] Xiehe Hosp Tangshan City, Dept Pathol, Tangshan City, Hebei Province, Peoples R China
关键词
MicroRNA-181b; Non-small cell lung cancer; Real-time quantitative RT-PCR assay; Prognosis; TUMOR-SUPPRESSOR; EXPRESSION; MIR-181B; SENSITIVITY; PROGRESSION; STATISTICS; SIGNATURES; GENE;
D O I
10.1016/j.prp.2013.04.018
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The aim of this study was to investigate the clinical significance of microRNA-181b (miR-181b) expression in non-small cell lung cancer (NSCLC). MiR-181b expression in 126 pairs of surgically removed NSCLC tissues and their corresponding normal lung tissues was measured by real-time quantitative RT-PCR assay. Additionally, the correlation of miR-181b expression with clinicopathological factors or prognosis of patients was analyzed. At first, miR-181b expression was significantly down-regulated in NSCLC tissues as compared with their normal counterparts (P<0.001). Then, the low miR-181b expression was found to be closely correlated with larger tumor size (P=0.02), higher p-TNM stage (P=0.008) and positive lymph node metastasis (P=0.03) of NSCLC patients. After that, survival analysis found that the overall survival (P=0.001) and disease-free survival (P=0.008) of NSCLC patients with low miR-181b expression were both significantly poorer compared to those patients with high miR-181b expression. Finally, both univariate and multivariate analyses demonstrated that low miR-181b expression may be a poor prognostic marker of NSCLC patients. This is the first study to indicate that down-regulation of miR-181b may be correlated with aggressive disease progression and poor prognosis of NSCLC patients, suggesting that miR-181b might be involved in lung carcinogenesis and become a potential prognostic marker for NSCLC. (C) 2013 Elsevier GmbH. All rights reserved.
引用
收藏
页码:490 / 494
页数:5
相关论文
共 32 条
[1]   Differential microRNA expression and identification of putative miRNA targets and pathways in head and neck cancers [J].
Ab Mutalib, Nurul-Syakima ;
Yoke-Kqueen, Cheah ;
Rahman, Sabariah Abdul ;
Sidik, Shiran Mohd ;
Singh, Avatar Singh Mohan ;
Learn-Han, Lee .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2011, 28 (03) :327-336
[2]  
[Anonymous], PRAC PREVENT MED
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   miRNA-181b increases the sensitivity of pancreatic ductal adenocarcinoma cells to gemcitabine in vitro and in nude mice by targeting BCL-2 [J].
Cai, Baobao ;
An, Yong ;
Lv, Nan ;
Chen, Jianmin ;
Tu, Min ;
Sun, Jie ;
Wu, Pengfei ;
Wei, Jishu ;
Jiang, Kuirong ;
Miao, Yi .
ONCOLOGY REPORTS, 2013, 29 (05) :1769-1776
[5]   MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866
[6]   MicroRNAs modulate hematopoietic lineage differentiation [J].
Chen, CZ ;
Li, L ;
Lodish, HF ;
Bartel, DP .
SCIENCE, 2004, 303 (5654) :83-86
[7]   MicroRNA-378 is associated with non-small cell lung cancer brain metastasis by promoting cell migration, invasion and tumor angiogenesis [J].
Chen, Lan-tao ;
Xu, Shi-dong ;
Xu, Hai ;
Zhang, Jin-feng ;
Ning, Jin-feng ;
Wang, Sheng-fa .
MEDICAL ONCOLOGY, 2012, 29 (03) :1673-1680
[8]   MicroRNA-181b targets cAMP responsive element binding protein 1 in gastric adenocarcinomas [J].
Chen, Lin ;
Yang, Qian ;
Kong, Wei-Qing ;
Liu, Tao ;
Liu, Min ;
Li, Xin ;
Tang, Hua .
IUBMB LIFE, 2012, 64 (07) :628-635
[9]   Extensive modulation of a set of microRNAs in primary glioblastoma [J].
Ciafrè, SA ;
Galardi, S ;
Mangiola, A ;
Ferracin, M ;
Liu, CG ;
Sabatino, G ;
Negrini, M ;
Maira, G ;
Croce, CM ;
Farace, MG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 334 (04) :1351-1358
[10]   MicroRNA-181b and microRNA-9 mediate arsenic-induced angiogenesis via NRP1 [J].
Cui, Yi ;
Han, Zhongji ;
Hu, Yi ;
Song, Ge ;
Hao, Chanjuan ;
Xia, Hongfei ;
Ma, Xu .
JOURNAL OF CELLULAR PHYSIOLOGY, 2012, 227 (02) :772-783