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
相关论文
共 45 条
[21]   Regulation of p53 expression by thymidylate synthase [J].
Ju, JF ;
Pedersen-Lane, J ;
Maley, F ;
Chu, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3769-3774
[22]   THE C-ELEGANS HETEROCHRONIC GENE LIN-4 ENCODES SMALL RNAS WITH ANTISENSE COMPLEMENTARITY TO LIN-14 [J].
LEE, RC ;
FEINBAUM, RL ;
AMBROS, V .
CELL, 1993, 75 (05) :843-854
[23]   Drug resistance, predictive markers and pharmacogenomics in colorectal cancer [J].
Longley, Daniel B. ;
Allen, Wendy L. ;
Johnston, Patrick G. .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2006, 1766 (02) :184-196
[24]   MicroRNA expression profiles classify human cancers [J].
Lu, J ;
Getz, G ;
Miska, EA ;
Alvarez-Saavedra, E ;
Lamb, J ;
Peck, D ;
Sweet-Cordero, A ;
Ebet, BL ;
Mak, RH ;
Ferrando, AA ;
Downing, JR ;
Jacks, T ;
Horvitz, HR ;
Golub, TR .
NATURE, 2005, 435 (7043) :834-838
[25]   Prognostic Significance of TRAIL Signaling Molecules in Stage II and III Colorectal Cancer [J].
McLornan, Donal P. ;
Barrett, Helen L. ;
Cummins, Robert ;
McDermott, Ultan ;
McDowell, Cliona ;
Conlon, Susie J. ;
Coyle, Victoria M. ;
Van Schaeybroeck, Sandra ;
Wilson, Richard ;
Kay, Elaine W. ;
Longley, Daniel B. ;
Johnston, Patrick G. .
CLINICAL CANCER RESEARCH, 2010, 16 (13) :3442-3451
[26]   Small RNAs Guide Hematopoietic Cell Differentiation and Function [J].
Navarro, Francisco ;
Lieberman, Judy .
JOURNAL OF IMMUNOLOGY, 2010, 184 (11) :5939-5947
[27]   CDK Inhibitor p21 Is Degraded by a Proliferating Cell Nuclear Antigen-coupled Cul4-DDB1Cdt2 Pathway during S Phase and after UV Irradiation [J].
Nishitani, Hideo ;
Shiomi, Yasushi ;
Iida, Hiroka ;
Michishita, Masato ;
Takami, Toshihiro ;
Tsurimoto, Toshiki .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (43) :29045-29052
[28]   Colon cancer survival rates with the new American Joint Committee on cancer sixth edition staging [J].
O'Connell, JB ;
Maggard, MA ;
Ko, CY .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (19) :1420-1425
[29]   Role of L2DTL, cell cycle-regulated nuclear and centrosome protein, in aggressive hepatocellular carcinoma [J].
Pan, Hung-Wei ;
Chou, Han-Yi E. ;
Liu, Shu-Hsiang ;
Peng, Shian-Yang ;
Liu, Chao-Lien ;
Hsu, Hey-Chi .
CELL CYCLE, 2006, 5 (22) :2676-2687
[30]   DTL/CDT2 is essential for both CDT1 regulation and the early G2/M checkpoint [J].
Sansam, Christopher L. ;
Shepard, Jennifer L. ;
Lai, Kevin ;
Ianari, Alessandra ;
Danielian, Paul S. ;
Amsterdam, Adam ;
Hopkins, Nancy ;
Lees, Jacqueline A. .
GENES & DEVELOPMENT, 2006, 20 (22) :3117-3129