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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
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.
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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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