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Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS
Non-small-cell lung cancer (NSCLC) constitutes approximately 80% of all diagnosed lung cancers, and diagnostic markers detectable in the plasma/serum of NSCLC patients are greatly needed. In this study, we established a pipeline for the discovery of markers using 9 transcriptome datasets from public...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570484/ https://www.ncbi.nlm.nih.gov/pubmed/28837649 http://dx.doi.org/10.1371/journal.pone.0183896 |
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author | Shin, Jihye Song, Sang-Yun Ahn, Hee-Sung An, Byung Chull Choi, Yoo-Duk Yang, Eun Gyeong Na, Kook-Joo Lee, Seung-Taek Park, Jae-Il Kim, Seon-Young Lee, Cheolju Lee, Seung-won |
author_facet | Shin, Jihye Song, Sang-Yun Ahn, Hee-Sung An, Byung Chull Choi, Yoo-Duk Yang, Eun Gyeong Na, Kook-Joo Lee, Seung-Taek Park, Jae-Il Kim, Seon-Young Lee, Cheolju Lee, Seung-won |
author_sort | Shin, Jihye |
collection | PubMed |
description | Non-small-cell lung cancer (NSCLC) constitutes approximately 80% of all diagnosed lung cancers, and diagnostic markers detectable in the plasma/serum of NSCLC patients are greatly needed. In this study, we established a pipeline for the discovery of markers using 9 transcriptome datasets from publicly available databases and profiling of six lung cancer cell secretomes. Thirty-one out of 312 proteins that overlapped between two-fold differentially expressed genes and identified cell secretome proteins were detected in the pooled plasma of lung cancer patients. To quantify the candidates in the serum of NSCLC patients, multiple-reaction-monitoring mass spectrometry (MRM-MS) was performed for five candidate biomarkers. Finally, two potential biomarkers (BCHE and GPx3; AUC = 0.713 and 0.673, respectively) and one two-marker panel generated by logistic regression (BCHE/GPx3; AUC = 0.773) were identified. A validation test was performed by ELISA to evaluate the reproducibility of GPx3 and BCHE expression in an independent set of samples (BCHE and GPx3; AUC = 0.630 and 0.759, respectively, BCHE/GPx3 panel; AUC = 0.788). Collectively, these results demonstrate the feasibility of using our pipeline for marker discovery and our MRM-MS platform for verifying potential biomarkers of human diseases. |
format | Online Article Text |
id | pubmed-5570484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55704842017-09-09 Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS Shin, Jihye Song, Sang-Yun Ahn, Hee-Sung An, Byung Chull Choi, Yoo-Duk Yang, Eun Gyeong Na, Kook-Joo Lee, Seung-Taek Park, Jae-Il Kim, Seon-Young Lee, Cheolju Lee, Seung-won PLoS One Research Article Non-small-cell lung cancer (NSCLC) constitutes approximately 80% of all diagnosed lung cancers, and diagnostic markers detectable in the plasma/serum of NSCLC patients are greatly needed. In this study, we established a pipeline for the discovery of markers using 9 transcriptome datasets from publicly available databases and profiling of six lung cancer cell secretomes. Thirty-one out of 312 proteins that overlapped between two-fold differentially expressed genes and identified cell secretome proteins were detected in the pooled plasma of lung cancer patients. To quantify the candidates in the serum of NSCLC patients, multiple-reaction-monitoring mass spectrometry (MRM-MS) was performed for five candidate biomarkers. Finally, two potential biomarkers (BCHE and GPx3; AUC = 0.713 and 0.673, respectively) and one two-marker panel generated by logistic regression (BCHE/GPx3; AUC = 0.773) were identified. A validation test was performed by ELISA to evaluate the reproducibility of GPx3 and BCHE expression in an independent set of samples (BCHE and GPx3; AUC = 0.630 and 0.759, respectively, BCHE/GPx3 panel; AUC = 0.788). Collectively, these results demonstrate the feasibility of using our pipeline for marker discovery and our MRM-MS platform for verifying potential biomarkers of human diseases. Public Library of Science 2017-08-24 /pmc/articles/PMC5570484/ /pubmed/28837649 http://dx.doi.org/10.1371/journal.pone.0183896 Text en © 2017 Shin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Shin, Jihye Song, Sang-Yun Ahn, Hee-Sung An, Byung Chull Choi, Yoo-Duk Yang, Eun Gyeong Na, Kook-Joo Lee, Seung-Taek Park, Jae-Il Kim, Seon-Young Lee, Cheolju Lee, Seung-won Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS |
title | Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS |
title_full | Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS |
title_fullStr | Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS |
title_full_unstemmed | Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS |
title_short | Integrative analysis for the discovery of lung cancer serological markers and validation by MRM-MS |
title_sort | integrative analysis for the discovery of lung cancer serological markers and validation by mrm-ms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570484/ https://www.ncbi.nlm.nih.gov/pubmed/28837649 http://dx.doi.org/10.1371/journal.pone.0183896 |
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