A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material

被引:21
|
作者
Bediaga, N. G. [1 ,2 ]
Davies, M. P. A. [1 ]
Acha-Sagredo, A. [3 ,4 ]
Hyde, R. [1 ]
Raji, O. Y. [1 ]
Page, R. [5 ]
Walshaw, M. [6 ]
Gosney, J. [7 ]
Alfirevic, A. [8 ]
Field, J. K. [1 ]
Liloglou, T. [1 ]
机构
[1] Univ Liverpool, Inst Translat Med, Dept Mol & Clin Canc Med, Roy Castle Lung Canc Res Programme, Liverpool L69 3BX, Merseyside, England
[2] Univ Basque Country, BIOMICs Res Grp, Vitoria, Spain
[3] Univ Basque Country, Dept Stomatol 2, UFI 11 25, Leioa, Spain
[4] Basque Fdn Sci, IKERBASQUE, Bilbao, Spain
[5] Liverpool Heart & Chest Hosp, Dept Thorac Surg, Liverpool, Merseyside, England
[6] Liverpool Heart & Chest Hosp, Dept Resp Med, Liverpool, Merseyside, England
[7] Royal Liverpool & Broadgreen Univ Hosp Trust, Dept Pathol, Liverpool, Merseyside, England
[8] Univ Liverpool, Inst Translat Med, Dept Mol & Clin Pharmacol, Liverpool L69 3BX, Merseyside, England
关键词
EPIGENETICALLY SILENCED MICRORNA; DNA METHYLATION; E-CADHERIN; CANCER; EXPRESSION; PROGNOSIS; FAMILY; SPUTUM; PANEL; GENE;
D O I
10.1038/bjc.2013.623
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Diagnosis is jeopardised when limited biopsy material is available or histological quality compromised. Here we developed and validated a prediction algorithm based on microRNA (miRNA) expression that can assist clinical diagnosis of lung cancer in minimal biopsy material to improve clinical management. Methods: Discovery utilised Taqman Low Density Arrays (754 miRNAs) in 20 non-small cell lung cancer (NSCLC) tumour/normal pairs. In an independent set of 40 NSCLC patients, 28 miRNA targets were validated using qRT-PCR. A prediction algorithm based on eight miRNA targets was validated blindly in a third independent set of 47 NSCLC patients. The panel was also tested in formalin-fixed paraffin-embedded (FFPE) specimens from 20 NSCLC patients. The genomic methylation status of highly deregulated miRNAs was investigated by pyrosequencing. Results: In the final, frozen validation set the panel had very high sensitivity (97.5%), specificity (96.3%) and ROC-AUC (0.99, P = 10(-15)). The panel provided 100% sensitivity and 95% specificity in FFPE tissue (ROC-AUC 0.97 (P = 10(-6))). DNA methylation abnormalities contribute little to the deregulation of the miRNAs tested. Conclusion: The developed prediction algorithm is a valuable potential biomarker for assisting lung cancer diagnosis in minimal biopsy material. A prospective validation is required to measure the enhancement of diagnostic accuracy of our current clinical practice.
引用
收藏
页码:2404 / 2411
页数:8
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