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Serum and Plasma Metabolomic Biomarkers for Lung Cancer

In drug invention and early disease prediction of lung cancer, metabolomic biomarker detection is very important. Mortality rate can be decreased, if cancer is predicted at the earlier stage. Recent diagnostic techniques for lung cancer are not prognosis diagnostic techniques. However, if we know th...

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Autores principales: Kumar, Nishith, Shahjaman, Md., Mollah, Md. Nurul Haque, Islam, S. M. Shahinul, Hoque, Md. Aminul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512859/
https://www.ncbi.nlm.nih.gov/pubmed/28729763
http://dx.doi.org/10.6026/97320630013202
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author Kumar, Nishith
Shahjaman, Md.
Mollah, Md. Nurul Haque
Islam, S. M. Shahinul
Hoque, Md. Aminul
author_facet Kumar, Nishith
Shahjaman, Md.
Mollah, Md. Nurul Haque
Islam, S. M. Shahinul
Hoque, Md. Aminul
author_sort Kumar, Nishith
collection PubMed
description In drug invention and early disease prediction of lung cancer, metabolomic biomarker detection is very important. Mortality rate can be decreased, if cancer is predicted at the earlier stage. Recent diagnostic techniques for lung cancer are not prognosis diagnostic techniques. However, if we know the name of the metabolites, whose intensity levels are considerably changing between cancer subject and control subject, then it will be easy to early diagnosis the disease as well as to discover the drug. Therefore, in this paper we have identified the influential plasma and serum blood sample metabolites for lung cancer and also identified the biomarkers that will be helpful for early disease prediction as well as for drug invention. To identify the influential metabolites, we considered a parametric and a nonparametric test namely student׳s t-test as parametric and Kruskal-Wallis test as non-parametric test. We also categorized the up-regulated and down-regulated metabolites by the heatmap plot and identified the biomarkers by support vector machine (SVM) classifier and pathway analysis. From our analysis, we got 27 influential (p-value<0.05) metabolites from plasma sample and 13 influential (p-value<0.05) metabolites from serum sample. According to the importance plot through SVM classifier, pathway analysis and correlation network analysis, we declared 4 metabolites (taurine, aspertic acid, glutamine and pyruvic acid) as plasma biomarker and 3 metabolites (aspartic acid, taurine and inosine) as serum biomarker.
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spelling pubmed-55128592017-07-20 Serum and Plasma Metabolomic Biomarkers for Lung Cancer Kumar, Nishith Shahjaman, Md. Mollah, Md. Nurul Haque Islam, S. M. Shahinul Hoque, Md. Aminul Bioinformation Hypothesis In drug invention and early disease prediction of lung cancer, metabolomic biomarker detection is very important. Mortality rate can be decreased, if cancer is predicted at the earlier stage. Recent diagnostic techniques for lung cancer are not prognosis diagnostic techniques. However, if we know the name of the metabolites, whose intensity levels are considerably changing between cancer subject and control subject, then it will be easy to early diagnosis the disease as well as to discover the drug. Therefore, in this paper we have identified the influential plasma and serum blood sample metabolites for lung cancer and also identified the biomarkers that will be helpful for early disease prediction as well as for drug invention. To identify the influential metabolites, we considered a parametric and a nonparametric test namely student׳s t-test as parametric and Kruskal-Wallis test as non-parametric test. We also categorized the up-regulated and down-regulated metabolites by the heatmap plot and identified the biomarkers by support vector machine (SVM) classifier and pathway analysis. From our analysis, we got 27 influential (p-value<0.05) metabolites from plasma sample and 13 influential (p-value<0.05) metabolites from serum sample. According to the importance plot through SVM classifier, pathway analysis and correlation network analysis, we declared 4 metabolites (taurine, aspertic acid, glutamine and pyruvic acid) as plasma biomarker and 3 metabolites (aspartic acid, taurine and inosine) as serum biomarker. Biomedical Informatics 2017-06-30 /pmc/articles/PMC5512859/ /pubmed/28729763 http://dx.doi.org/10.6026/97320630013202 Text en © 2017 Biomedical Informatics http://creativecommons.org/licenses/by/3.0/ This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.
spellingShingle Hypothesis
Kumar, Nishith
Shahjaman, Md.
Mollah, Md. Nurul Haque
Islam, S. M. Shahinul
Hoque, Md. Aminul
Serum and Plasma Metabolomic Biomarkers for Lung Cancer
title Serum and Plasma Metabolomic Biomarkers for Lung Cancer
title_full Serum and Plasma Metabolomic Biomarkers for Lung Cancer
title_fullStr Serum and Plasma Metabolomic Biomarkers for Lung Cancer
title_full_unstemmed Serum and Plasma Metabolomic Biomarkers for Lung Cancer
title_short Serum and Plasma Metabolomic Biomarkers for Lung Cancer
title_sort serum and plasma metabolomic biomarkers for lung cancer
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512859/
https://www.ncbi.nlm.nih.gov/pubmed/28729763
http://dx.doi.org/10.6026/97320630013202
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