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The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion
For malignant pleural effusions, pleural fluid cytology is a diagnostic method, but sensitivity is low. The pleural fluid contains metabolites directly released from cancer cells. The objective of this study was to diagnose lung cancer with malignant pleural effusion using the volatilomic profiling...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245642/ https://www.ncbi.nlm.nih.gov/pubmed/34193905 http://dx.doi.org/10.1038/s41598-021-93032-y |
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author | Chen, Ke-Cheng Tsai, Shih-Wei Zhang, Xiang Zeng, Chian Yang, Hsiao-Yu |
author_facet | Chen, Ke-Cheng Tsai, Shih-Wei Zhang, Xiang Zeng, Chian Yang, Hsiao-Yu |
author_sort | Chen, Ke-Cheng |
collection | PubMed |
description | For malignant pleural effusions, pleural fluid cytology is a diagnostic method, but sensitivity is low. The pleural fluid contains metabolites directly released from cancer cells. The objective of this study was to diagnose lung cancer with malignant pleural effusion using the volatilomic profiling method. We recruited lung cancer patients with malignant pleural effusion and patients with nonmalignant diseases with pleural effusion as controls. We analyzed the headspace air of the pleural effusion by gas chromatography-mass spectrometry. We used partial least squares discriminant analysis (PLS-DA) to identify metabolites and the support vector machine (SVM) to establish the prediction model. We split data into a training set (80%) and a testing set (20%) to validate the accuracy. A total of 68 subjects were included in the final analysis. The PLS-DA showed high discrimination with an R(2) of 0.95 and Q(2) of 0.58. The accuracy of the SVM in the test set was 0.93 (95% CI 0.66, 0.998), the sensitivity was 83%, the specificity was 100%, and kappa was 0.85, and the area under the receiver operating characteristic curve was 0.96 (95% CI 0.86, 1.00). Volatile metabolites of pleural effusion might be used in patients with cytology-negative pleural effusion to rule out malignancy. |
format | Online Article Text |
id | pubmed-8245642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82456422021-07-06 The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion Chen, Ke-Cheng Tsai, Shih-Wei Zhang, Xiang Zeng, Chian Yang, Hsiao-Yu Sci Rep Article For malignant pleural effusions, pleural fluid cytology is a diagnostic method, but sensitivity is low. The pleural fluid contains metabolites directly released from cancer cells. The objective of this study was to diagnose lung cancer with malignant pleural effusion using the volatilomic profiling method. We recruited lung cancer patients with malignant pleural effusion and patients with nonmalignant diseases with pleural effusion as controls. We analyzed the headspace air of the pleural effusion by gas chromatography-mass spectrometry. We used partial least squares discriminant analysis (PLS-DA) to identify metabolites and the support vector machine (SVM) to establish the prediction model. We split data into a training set (80%) and a testing set (20%) to validate the accuracy. A total of 68 subjects were included in the final analysis. The PLS-DA showed high discrimination with an R(2) of 0.95 and Q(2) of 0.58. The accuracy of the SVM in the test set was 0.93 (95% CI 0.66, 0.998), the sensitivity was 83%, the specificity was 100%, and kappa was 0.85, and the area under the receiver operating characteristic curve was 0.96 (95% CI 0.86, 1.00). Volatile metabolites of pleural effusion might be used in patients with cytology-negative pleural effusion to rule out malignancy. Nature Publishing Group UK 2021-06-30 /pmc/articles/PMC8245642/ /pubmed/34193905 http://dx.doi.org/10.1038/s41598-021-93032-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chen, Ke-Cheng Tsai, Shih-Wei Zhang, Xiang Zeng, Chian Yang, Hsiao-Yu The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
title | The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
title_full | The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
title_fullStr | The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
title_full_unstemmed | The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
title_short | The investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
title_sort | investigation of the volatile metabolites of lung cancer from the microenvironment of malignant pleural effusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245642/ https://www.ncbi.nlm.nih.gov/pubmed/34193905 http://dx.doi.org/10.1038/s41598-021-93032-y |
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