Clinicopathological and Prognostic Value of MicroRNA-21 and MicroRNA-155 in Colorectal Cancer

被引:215
作者
Shibuya, Hajime [1 ]
Iinuma, Hisae [1 ]
Shimada, Ryu [1 ]
Horiuchi, Atsushi [1 ]
Watanabe, Toshiaki [1 ]
机构
[1] Teikyo Univ, Dept Surg, Sch Med, Itabashi Ku, Tokyo 1730003, Japan
关键词
Colorectal cancer; MicroRNA-21; MicroRNA-155; PDCD4; Prognostic factor; TP53INP1; TUMOR-SUPPRESSOR PDCD4; EXPRESSION; MIR-21; TRANSFORMATION; METASTASIS; PROFILES; FEATURES; MIRNAS; GENE;
D O I
10.1159/000323283
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The clinical significance of microRNA-21 (miR-21) and miR-155 in colorectal cancer (CRC) patients remains elusive. In this study, we established the prognostic value of miR-21 and miR-155 using clinical samples from CRC patients. Furthermore, relationships between these microRNAs and target genes (PDCD4 and TP53INP1 mRNAs) were examined. Methods: miR-21 and miR-155 expression was assessed in tumor tissue and in adjacent normal tissue of 156 CRC patients by TaqMan MicroRNA assays, and PDCD4 and TP53INP1 mRNA levels were measured by quantitative real-time reverse transcriptase PCR (RT-PCR). Results: High miR21 expression was significantly associated with venous invasion, liver metastasis and tumor stage, and high miR-155 expression was significantly correlated with lymph node metastases. The overall (OS) and disease-free survival (DFS) rates of patients with high miR-21 expression were significantly worse than those of patients with low miR-21 expression. The OS and DFS of patients with high miR-155 expression were also significantly worse than those in patients with low miR-155 expression. miR-21 and miR-155 expression levels in CRC tissue were independent prognostic factors for OS and DFS. Significant inverse correlations were demonstrated between miR-21 and PDCD4 mRNA, and miR-155 and TP53INP1 mRNA. Conclusion: Increases in miR-21 and miR155 expression may represent effective biomarkers for the prediction of a poor prognosis. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:313 / 320
页数:8
相关论文
共 35 条
[21]   New microRNAs from mouse and human [J].
Lagos-Quintana, M ;
Rauhut, R ;
Meyer, J ;
Borkhardt, A ;
Tuschl, T .
RNA, 2003, 9 (02) :175-179
[22]   Pdcd4 inhibits growth of tumor cells by suppression of carbonic anhydrase type II [J].
Lankat-Buttgereit, B ;
Gregel, C ;
Knolle, A ;
Hasilik, A ;
Arnold, R ;
Göke, R .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2004, 214 (1-2) :149-153
[23]   MicroRNA-21 promotes cell transformation by targeting the programmed cell death 4 gene [J].
Lu, Z. ;
Liu, M. ;
Stribinskis, V. ;
Klinge, C. M. ;
Ramos, K. S. ;
Colburn, N. H. ;
Li, Y. .
ONCOGENE, 2008, 27 (31) :4373-4379
[24]   MicroRNA-21 regulates expression of the PTEN tumor suppressor gene in human hepatocellular cancer [J].
Meng, Fanyin ;
Henson, Roger ;
Wehbe-Janek, Hania ;
Ghoshal, Kalpana ;
Jacob, Samson T. ;
Patel, Tushar .
GASTROENTEROLOGY, 2007, 133 (02) :647-658
[25]   Clinicopathological and prognostic significance of PDCD4 and microRNA-21 in human gastric cancer [J].
Motoyama, Kazuo ;
Inoue, Hiroshi ;
Mimori, Koshi ;
Tanaka, Fumiaki ;
Kojima, Kazuyuki ;
Uetake, Hiroyuki ;
Sugihara, Kenichi ;
Mori, Masaki .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 36 (05) :1089-1095
[26]   MicroRNA Classifiers for Predicting Prognosis of Squamous Cell Lung Cancer [J].
Raponi, Mitch ;
Dossey, Lesley ;
Jatkoe, Tim ;
Wu, Xiaoying ;
Chen, Guoan ;
Fan, Hongtao ;
Beer, David G. .
CANCER RESEARCH, 2009, 69 (14) :5776-5783
[27]   MicroRNA expression abnormalities in pancreatic endocrine and acinar tumors are associated with distinctive pathologic features and clinical behavior [J].
Roldo, Claudia ;
Missiaglia, Edoardo ;
Hagan, John P. ;
Falconi, Massimo ;
Capelli, Paola ;
Bersani, Samantha ;
Calin, George Adrian ;
Volinia, Stefano ;
Liu, Chang-Gong ;
Scarpa, Aldo ;
Croce, Carlo M. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (29) :4677-4684
[28]   MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma [J].
Schetter, Aaron J. ;
Leung, Suet Yi ;
Sohn, Jane J. ;
Zanetti, Krista A. ;
Bowman, Elise D. ;
Yanaihara, Nozomu ;
Yuen, Siu Tsan ;
Chan, Tsun Leung ;
Kwong, Dora L. W. ;
Au, Gordon K. H. ;
Liu, Chang-Gong ;
Calin, George A. ;
Croce, Carlo M. ;
Harris, Curtis C. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2008, 299 (04) :425-436
[29]  
SHIKE M, 1990, B WORLD HEALTH ORGAN, V68, P377
[30]   Altered expression of miR-21, miR-31, miR-143 and miR-145 is related to clinicopathologic features of colorectal cancer [J].
Slaby, O. ;
Svoboda, M. ;
Fabian, P. ;
Smerdova, T. ;
Knoflickova, D. ;
Bednarikova, M. ;
Nenutil, R. ;
Vyzula, R. .
ONCOLOGY, 2007, 72 (5-6) :397-402