Circulating miRNAs miR-34a and miR-150 associated with colorectal cancer progression

被引:84
|
作者
Aherne, Sinead T. [1 ]
Madden, Stephen F. [1 ]
Hughes, David J. [2 ,3 ]
Pardini, Barbara [4 ]
Naccarati, Alessio [4 ,7 ]
Levy, Miroslav [5 ,6 ]
Vodicka, Pavel [7 ]
Neary, Paul [8 ]
Dowling, Paul [1 ,9 ]
Clynes, Martin [1 ]
机构
[1] Dublin City Univ, Natl Inst Cellular Biotechnol, Mol Therapeut Canc Ireland, Dublin 9, Ireland
[2] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Dublin 2, Ireland
[3] Royal Coll Surgeons Ireland, Ctr Syst Med, Dublin 2, Ireland
[4] Human Genet Fdn, Turin, Italy
[5] Charles Univ Prague, Fac Med 1, Prague, Czech Republic
[6] Thomayer Hosp, Prague, Czech Republic
[7] Acad Sci Czech Republ, Inst Expt Med, Prague, Czech Republic
[8] AMNCH Hosp, Dept Colorectal Surg, Dublin 24, Ireland
[9] Maynooth Univ, Dept Biol, Maynooth, Kildare, Ireland
基金
爱尔兰科学基金会;
关键词
Colorectal cancer; Circulating miRNAs; miR-34a; miR-150; miR-923; MICRORNAS; BIOMARKERS; EXPRESSION; PLASMA; SERUM; CELLS; MIR-29A; MARKER; COLON;
D O I
10.1186/s12885-015-1327-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Screening for the early detection of colorectal cancer is important to improve patient survival. The aim of this study was to investigate the potential of circulating cell-free miRNAs as biomarkers of CRC, and their efficiency at delineating patients with polyps and benign adenomas from normal and cancer patient groups. Methods: The expression of 667 miRNAs was assessed in a discovery set of 48 plasma samples comprising normal, polyp, adenoma, and early and advanced cancer samples. Three miRNAs (miR-34a, miR-150, and miR-923) were further examined in a validation cohort of 97 subjects divided into the same five groups, and in an independent public dataset of 40 CRC samples and paired normal tissues. Results: High levels of circulating miR-34a and low miR-150 levels distinguished groups of patients with polyps from those with advanced cancer (AUC = 0.904), and low circulating miR-150 levels separated patients with adenomas from those with advanced cancer (AUC = 0.875). In addition, the altered expression of miR-34a and miR-150 in an independent public dataset of forty CRC samples and paired normal tissues was confirmed. Conclusion: We identified two circulating miRNAs capable of distinguishing patient groups with different diseases of the colon from each other, and patients with advanced cancer from benign disease groups.
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页数:13
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