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A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material
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 clin...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817343/ https://www.ncbi.nlm.nih.gov/pubmed/24113142 http://dx.doi.org/10.1038/bjc.2013.623 |
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author | Bediaga, N G Davies, M P A Acha-Sagredo, A Hyde, R Raji, O Y Page, R Walshaw, M Gosney, J Alfirevic, A Field, J K Liloglou, T |
author_facet | Bediaga, N G Davies, M P A Acha-Sagredo, A Hyde, R Raji, O Y Page, R Walshaw, M Gosney, J Alfirevic, A Field, J K Liloglou, T |
author_sort | Bediaga, N G |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3817343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-38173432014-10-29 A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material Bediaga, N G Davies, M P A Acha-Sagredo, A Hyde, R Raji, O Y Page, R Walshaw, M Gosney, J Alfirevic, A Field, J K Liloglou, T Br J Cancer Molecular Diagnostics 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. Nature Publishing Group 2013-10-29 2013-10-10 /pmc/articles/PMC3817343/ /pubmed/24113142 http://dx.doi.org/10.1038/bjc.2013.623 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Molecular Diagnostics Bediaga, N G Davies, M P A Acha-Sagredo, A Hyde, R Raji, O Y Page, R Walshaw, M Gosney, J Alfirevic, A Field, J K Liloglou, T A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
title | A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
title_full | A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
title_fullStr | A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
title_full_unstemmed | A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
title_short | A microRNA-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
title_sort | microrna-based prediction algorithm for diagnosis of non-small lung cell carcinoma in minimal biopsy material |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817343/ https://www.ncbi.nlm.nih.gov/pubmed/24113142 http://dx.doi.org/10.1038/bjc.2013.623 |
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