Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study

<i>Background</i>: Lung cancer is the most common cause of cancer-related deaths worldwide. Early diagnosis is crucial to increase the curability chance of the patients. Low dose CT screening can reduce lung cancer mortality, but it is associated with several limitations. Metabolomics is...

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Main Authors: Sandeep Singhal, Christian Rolfo, Andrew W. Maksymiuk, Paramjit S. Tappia, Daniel S. Sitar, Alessandro Russo, Parveen S. Akhtar, Nazrina Khatun, Parveen Rahnuma, Ahmed Rashiduzzaman, Rashid Ahmed Bux, Guoyu Huang, Bram Ramjiawan
Format: Article
Language:English
Published: MDPI AG 2019-07-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/11/8/1069
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spelling doaj-2787fde1005a4a3fabd753dfbbc3a2e02020-11-24T21:21:38ZengMDPI AGCancers2072-66942019-07-01118106910.3390/cancers11081069cancers11081069Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot StudySandeep Singhal0Christian Rolfo1Andrew W. Maksymiuk2Paramjit S. Tappia3Daniel S. Sitar4Alessandro Russo5Parveen S. Akhtar6Nazrina Khatun7Parveen Rahnuma8Ahmed Rashiduzzaman9Rashid Ahmed Bux10Guoyu Huang11Bram Ramjiawan12Columbia University Medical Center, New York, NY 10032, USAMarlene and Stewart Greenebaum Comprehensive Cancer Centre, University of Maryland, Baltimore, MD 21201, USACancer Care Manitoba, Winnipeg, MB R3E 0V9, CanadaAsper Clinical Research Institute &amp; Office of Clinical Research, St. Boniface Hospital, Winnipeg, MB R2H 2A6, CanadaDepartment of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3A 1R9, CanadaMarlene and Stewart Greenebaum Comprehensive Cancer Centre, University of Maryland, Baltimore, MD 21201, USADepartment of Medical Oncology, National Institute of Cancer Research &amp; Hospital, Mohakhali, 1221 Dhaka, BangladeshDepartment of Medical Oncology, National Institute of Cancer Research &amp; Hospital, Mohakhali, 1221 Dhaka, BangladeshDepartment of Medical Oncology, National Institute of Cancer Research &amp; Hospital, Mohakhali, 1221 Dhaka, BangladeshFastBios, House 12, Rd 14/C, Sector 4, Uttara, 1230 Dhaka, BangladeshBioMark Diagnostics Inc., Richmond, BC V6X 2W8, CanadaBioMark Diagnostics Inc., Richmond, BC V6X 2W8, CanadaAsper Clinical Research Institute &amp; Office of Clinical Research, St. Boniface Hospital, Winnipeg, MB R2H 2A6, Canada<i>Background</i>: Lung cancer is the most common cause of cancer-related deaths worldwide. Early diagnosis is crucial to increase the curability chance of the patients. Low dose CT screening can reduce lung cancer mortality, but it is associated with several limitations. Metabolomics is a promising technique for cancer diagnosis due to its ability to provide chemical phenotyping data. The intent of our study was to explore metabolomic effects and profiles of lung cancer patients to determine if metabolic perturbations in the SSAT-1/polyamine pathway can distinguish between healthy participants and lung cancer patients as a diagnostic and treatment monitoring tool. <i>Patients and Methods</i>: Plasma samples were collected as part of the SSAT1 Amantadine Cancer Study. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to identify and quantify metabolite concentrations in lung cancer patient and control samples. Standard statistical analyses were performed to determine whether metabolite concentrations could differentiate between healthy subjects and lung cancer patients, as well as risk prediction modeling applied to determine whether metabolic profiles could provide an indication of cancer progression in later stage patients. <i>Results</i>: A panel consisting of 14 metabolites, which included 6 metabolites in the polyamine pathway, was identified that correctly discriminated lung cancer patients from controls with an area under the curve of 0.97 (95% CI: 0.875-1.0). <b>Conclusion:</b> When used in conjunction with the SSAT-1/polyamine pathway, these metabolites may provide the specificity required for diagnosing lung cancer from other cancer types and could be used as a diagnostic and treatment monitoring tool.https://www.mdpi.com/2072-6694/11/8/1069metabolomicslung cancermetabolomic fingerprintNSCLCpolyamineSSAT-1
collection DOAJ
language English
format Article
sources DOAJ
author Sandeep Singhal
Christian Rolfo
Andrew W. Maksymiuk
Paramjit S. Tappia
Daniel S. Sitar
Alessandro Russo
Parveen S. Akhtar
Nazrina Khatun
Parveen Rahnuma
Ahmed Rashiduzzaman
Rashid Ahmed Bux
Guoyu Huang
Bram Ramjiawan
spellingShingle Sandeep Singhal
Christian Rolfo
Andrew W. Maksymiuk
Paramjit S. Tappia
Daniel S. Sitar
Alessandro Russo
Parveen S. Akhtar
Nazrina Khatun
Parveen Rahnuma
Ahmed Rashiduzzaman
Rashid Ahmed Bux
Guoyu Huang
Bram Ramjiawan
Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study
Cancers
metabolomics
lung cancer
metabolomic fingerprint
NSCLC
polyamine
SSAT-1
author_facet Sandeep Singhal
Christian Rolfo
Andrew W. Maksymiuk
Paramjit S. Tappia
Daniel S. Sitar
Alessandro Russo
Parveen S. Akhtar
Nazrina Khatun
Parveen Rahnuma
Ahmed Rashiduzzaman
Rashid Ahmed Bux
Guoyu Huang
Bram Ramjiawan
author_sort Sandeep Singhal
title Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study
title_short Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study
title_full Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study
title_fullStr Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study
title_full_unstemmed Liquid Biopsy in Lung Cancer Screening: The Contribution of Metabolomics. Results of A Pilot Study
title_sort liquid biopsy in lung cancer screening: the contribution of metabolomics. results of a pilot study
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2019-07-01
description <i>Background</i>: Lung cancer is the most common cause of cancer-related deaths worldwide. Early diagnosis is crucial to increase the curability chance of the patients. Low dose CT screening can reduce lung cancer mortality, but it is associated with several limitations. Metabolomics is a promising technique for cancer diagnosis due to its ability to provide chemical phenotyping data. The intent of our study was to explore metabolomic effects and profiles of lung cancer patients to determine if metabolic perturbations in the SSAT-1/polyamine pathway can distinguish between healthy participants and lung cancer patients as a diagnostic and treatment monitoring tool. <i>Patients and Methods</i>: Plasma samples were collected as part of the SSAT1 Amantadine Cancer Study. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to identify and quantify metabolite concentrations in lung cancer patient and control samples. Standard statistical analyses were performed to determine whether metabolite concentrations could differentiate between healthy subjects and lung cancer patients, as well as risk prediction modeling applied to determine whether metabolic profiles could provide an indication of cancer progression in later stage patients. <i>Results</i>: A panel consisting of 14 metabolites, which included 6 metabolites in the polyamine pathway, was identified that correctly discriminated lung cancer patients from controls with an area under the curve of 0.97 (95% CI: 0.875-1.0). <b>Conclusion:</b> When used in conjunction with the SSAT-1/polyamine pathway, these metabolites may provide the specificity required for diagnosing lung cancer from other cancer types and could be used as a diagnostic and treatment monitoring tool.
topic metabolomics
lung cancer
metabolomic fingerprint
NSCLC
polyamine
SSAT-1
url https://www.mdpi.com/2072-6694/11/8/1069
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