Prognostic Significance of miR-215 in Colon Cancer

被引:129
作者
Karaayvaz, Mihriban
Pal, Timothy
Song, Bo
Zhang, Cecilia [2 ]
Georgakopoulos, Penelope
Mehmood, Saira
Burke, Stephanie
Shroyer, Kenneth
Ju, Jingfang [1 ]
机构
[1] SUNY Stony Brook, Translat Res Lab, Dept Pathol, Med Ctr, Stony Brook, NY 11794 USA
[2] NYU, New York, NY USA
关键词
Biomarker; Colon cancer; MicroRNA; Prognosis; THYMIDYLATE SYNTHASE; MICRORNA EXPRESSION; CELL-PROLIFERATION; SMALL RNAS; GENE-EXPRESSION; P53; CHEMORESISTANCE; OSTEOSARCOMA; MIR-34A; PROTEIN;
D O I
10.1016/j.clcc.2011.06.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The clinical utility of miR-215 as a potential biomarker in colon cancer was investigated. The levels of miR-215 were quantified by real-time qRT-PCR in 34 paired normal and tumor specimens. The expression levels of miR-215 were decreased in colon tumors, and were associated with patient survival. Thus, miR-215 is a potential prognostic biomarker in colon cancer. Background: We have previously shown that miR-215 suppressed the expression of key targets such as thymidylate synthase (TS), dihydrofolate reductase, and denticleless protein homolog (DTL) in colon cancer. miR-215 is a tumor suppressor candidate due to the upregulation of p53 and p21 by targeting DTL. However, high levels of miR-215 conferred chemoresistance due to cell cycle arrest and reduced cell proliferation by suppressing DTL. In this study, the clinical significance of miR-215 was further investigated as a potential prognostic biomarker in colon cancer patients. Methods: Total RNAs were extracted from 34 paired normal and colon (stage II and III) tumor specimens using the Trizol-based approach. The levels of miR-215 and a closely related miR-192 were quantified using quantitative real-time polymerase chain reaction (qRT-PCR) expression analysis. The expression of DTL mRNA and protein were quantified by real time qRT-PCR and immunohistochemistry. Results: The expression levels of miR-192 (P = .0008) and miR-215 (P < .0001) were significantly decreased in colon tumors compared with normal tissues. DTL was significantly over-expressed and was inversely correlated with miR-215, further suggesting an in vivo physiologic relevance of miR-215 mediated DTL suppression. Kaplan-Meier survival analysis by Cox regression revealed that high levels of miR-215 expression (hazard ratio, 3.516; 95% confidence interval, 1.007-12.28, P = .025) are closely associated with poor patient's overall survival. Furthermore, an elevated expression of a miR-215 target protein DTL was detected in colon cancer tissues whereas no expression was present in normal tissues. Conclusion: miR-215 has a unique potential as a prognostic biomarker in stage II and III colon cancer. Clinical Colorectal Cancer, Vol. 10, No. 4, 340-7 (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:340 / 347
页数:8
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