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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
来源:
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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