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Prognostic value of microRNA expression in operable non-small cell lung cancer patients
BACKGROUND: About 50% of non-small cell lung cancer (NSCLC) patients develop distant metastases following pulmonary resection. Currently, there are no reliable factors allowing for individual selection of high-risk patients for adjuvant systemic therapies. METHODS: We assessed by quantitative revers...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929871/ https://www.ncbi.nlm.nih.gov/pubmed/24448358 http://dx.doi.org/10.1038/bjc.2013.786 |
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author | Skrzypski, M Czapiewski, P Goryca, K Jassem, E Wyrwicz, L Pawłowski, R Rzyman, W Biernat, W Jassem, J |
author_facet | Skrzypski, M Czapiewski, P Goryca, K Jassem, E Wyrwicz, L Pawłowski, R Rzyman, W Biernat, W Jassem, J |
author_sort | Skrzypski, M |
collection | PubMed |
description | BACKGROUND: About 50% of non-small cell lung cancer (NSCLC) patients develop distant metastases following pulmonary resection. Currently, there are no reliable factors allowing for individual selection of high-risk patients for adjuvant systemic therapies. METHODS: We assessed by quantitative reverse transcription PCR microRNA (miRNA) expression in 273 stage I–IIIA NSCLC samples. Expression of 677 miRNAs was evaluated in fresh-frozen tumour samples in the training cohort of 50 squamous cell carcinoma (SCC) patients who underwent curative surgery. Of those, 20 patients developed distant metastases, and 30 were free of recurrence for >4 years. In the second step, miRNAs with highest predictive value for distant relapse were re-evaluated in formalin-fixed paraffin-embedded material in an independent group of 134 stage I–IIIA SCC patients. Additionally, the same miRNAs were investigated in 89 lung adenocarcinoma (AC) patients and in normal lung parenchyma (NLP). RESULTS: In the training cohort of SCC, six miRNAs were differently expressed in the non-recurrent vs recurrent groups and correlated with distant recurrence-free survival, however none reached the level of significance after correction for multiple testing. Of these six miRNAs, miR-662, -192 and -192* were confirmed as prognostic in the independent SCC cohort. Expression of miR-128, -10b, -502-3p and -192 differed between SCC and AC, and miR-128 and -192 – between NLP and NSCLC. CONCLUSIONS: We identified three new miRNAs predictive of distant relapse in operable SCC. Future miRNA studies should account for differences between NSCLC subtypes. |
format | Online Article Text |
id | pubmed-3929871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39298712015-02-18 Prognostic value of microRNA expression in operable non-small cell lung cancer patients Skrzypski, M Czapiewski, P Goryca, K Jassem, E Wyrwicz, L Pawłowski, R Rzyman, W Biernat, W Jassem, J Br J Cancer Molecular Diagnostics BACKGROUND: About 50% of non-small cell lung cancer (NSCLC) patients develop distant metastases following pulmonary resection. Currently, there are no reliable factors allowing for individual selection of high-risk patients for adjuvant systemic therapies. METHODS: We assessed by quantitative reverse transcription PCR microRNA (miRNA) expression in 273 stage I–IIIA NSCLC samples. Expression of 677 miRNAs was evaluated in fresh-frozen tumour samples in the training cohort of 50 squamous cell carcinoma (SCC) patients who underwent curative surgery. Of those, 20 patients developed distant metastases, and 30 were free of recurrence for >4 years. In the second step, miRNAs with highest predictive value for distant relapse were re-evaluated in formalin-fixed paraffin-embedded material in an independent group of 134 stage I–IIIA SCC patients. Additionally, the same miRNAs were investigated in 89 lung adenocarcinoma (AC) patients and in normal lung parenchyma (NLP). RESULTS: In the training cohort of SCC, six miRNAs were differently expressed in the non-recurrent vs recurrent groups and correlated with distant recurrence-free survival, however none reached the level of significance after correction for multiple testing. Of these six miRNAs, miR-662, -192 and -192* were confirmed as prognostic in the independent SCC cohort. Expression of miR-128, -10b, -502-3p and -192 differed between SCC and AC, and miR-128 and -192 – between NLP and NSCLC. CONCLUSIONS: We identified three new miRNAs predictive of distant relapse in operable SCC. Future miRNA studies should account for differences between NSCLC subtypes. Nature Publishing Group 2014-02-18 2014-01-21 /pmc/articles/PMC3929871/ /pubmed/24448358 http://dx.doi.org/10.1038/bjc.2013.786 Text en Copyright © 2014 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 Skrzypski, M Czapiewski, P Goryca, K Jassem, E Wyrwicz, L Pawłowski, R Rzyman, W Biernat, W Jassem, J Prognostic value of microRNA expression in operable non-small cell lung cancer patients |
title | Prognostic value of microRNA expression in operable non-small cell lung cancer patients |
title_full | Prognostic value of microRNA expression in operable non-small cell lung cancer patients |
title_fullStr | Prognostic value of microRNA expression in operable non-small cell lung cancer patients |
title_full_unstemmed | Prognostic value of microRNA expression in operable non-small cell lung cancer patients |
title_short | Prognostic value of microRNA expression in operable non-small cell lung cancer patients |
title_sort | prognostic value of microrna expression in operable non-small cell lung cancer patients |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929871/ https://www.ncbi.nlm.nih.gov/pubmed/24448358 http://dx.doi.org/10.1038/bjc.2013.786 |
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