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Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum

BACKGROUND: Survival time for lung cancer is poor with over 90% of patients dying within five years of diagnosis primarily due to detection at late stage. The main objective of this study was to evaluate Fourier transform infrared spectroscopy (FTIR) as a high throughput and cost effective method fo...

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Autores principales: Lewis, Paul D, Lewis, Keir E, Ghosal, Robin, Bayliss, Sion, Lloyd, Amanda J, Wills, John, Godfrey, Ruth, Kloer, Philip, Mur, Luis AJ
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000851/
https://www.ncbi.nlm.nih.gov/pubmed/21092279
http://dx.doi.org/10.1186/1471-2407-10-640
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author Lewis, Paul D
Lewis, Keir E
Ghosal, Robin
Bayliss, Sion
Lloyd, Amanda J
Wills, John
Godfrey, Ruth
Kloer, Philip
Mur, Luis AJ
author_facet Lewis, Paul D
Lewis, Keir E
Ghosal, Robin
Bayliss, Sion
Lloyd, Amanda J
Wills, John
Godfrey, Ruth
Kloer, Philip
Mur, Luis AJ
author_sort Lewis, Paul D
collection PubMed
description BACKGROUND: Survival time for lung cancer is poor with over 90% of patients dying within five years of diagnosis primarily due to detection at late stage. The main objective of this study was to evaluate Fourier transform infrared spectroscopy (FTIR) as a high throughput and cost effective method for identifying biochemical changes in sputum as biomarkers for detection of lung cancer. METHODS: Sputum was collected from 25 lung cancer patients in the Medlung observational study and 25 healthy controls. FTIR spectra were generated from sputum cell pellets using infrared wavenumbers within the 1800 to 950 cm(-1 )"fingerprint" region. RESULTS: A panel of 92 infrared wavenumbers had absorbances significantly different between cancer and normal sputum spectra and were associated with putative changes in protein, nucleic acid and glycogen levels in tumours. Five prominent significant wavenumbers at 964 cm(-1), 1024 cm(-1), 1411 cm(-1), 1577 cm(-1 )and 1656 cm(-1 )separated cancer spectra from normal spectra into two distinct groups using multivariate analysis (group 1: 100% cancer cases; group 2: 92% normal cases). Principal components analysis revealed that these wavenumbers were also able to distinguish lung cancer patients who had previously been diagnosed with breast cancer. No patterns of spectra groupings were associated with inflammation or other diseases of the airways. CONCLUSIONS: Our results suggest that FTIR applied to sputum might have high sensitivity and specificity in diagnosing lung cancer with potential as a non-invasive, cost-effective and high-throughput method for screening. TRIAL REGISTRATION: ClinicalTrials.gov: NCT00899262
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spelling pubmed-30008512010-12-11 Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum Lewis, Paul D Lewis, Keir E Ghosal, Robin Bayliss, Sion Lloyd, Amanda J Wills, John Godfrey, Ruth Kloer, Philip Mur, Luis AJ BMC Cancer Research Article BACKGROUND: Survival time for lung cancer is poor with over 90% of patients dying within five years of diagnosis primarily due to detection at late stage. The main objective of this study was to evaluate Fourier transform infrared spectroscopy (FTIR) as a high throughput and cost effective method for identifying biochemical changes in sputum as biomarkers for detection of lung cancer. METHODS: Sputum was collected from 25 lung cancer patients in the Medlung observational study and 25 healthy controls. FTIR spectra were generated from sputum cell pellets using infrared wavenumbers within the 1800 to 950 cm(-1 )"fingerprint" region. RESULTS: A panel of 92 infrared wavenumbers had absorbances significantly different between cancer and normal sputum spectra and were associated with putative changes in protein, nucleic acid and glycogen levels in tumours. Five prominent significant wavenumbers at 964 cm(-1), 1024 cm(-1), 1411 cm(-1), 1577 cm(-1 )and 1656 cm(-1 )separated cancer spectra from normal spectra into two distinct groups using multivariate analysis (group 1: 100% cancer cases; group 2: 92% normal cases). Principal components analysis revealed that these wavenumbers were also able to distinguish lung cancer patients who had previously been diagnosed with breast cancer. No patterns of spectra groupings were associated with inflammation or other diseases of the airways. CONCLUSIONS: Our results suggest that FTIR applied to sputum might have high sensitivity and specificity in diagnosing lung cancer with potential as a non-invasive, cost-effective and high-throughput method for screening. TRIAL REGISTRATION: ClinicalTrials.gov: NCT00899262 BioMed Central 2010-11-23 /pmc/articles/PMC3000851/ /pubmed/21092279 http://dx.doi.org/10.1186/1471-2407-10-640 Text en Copyright ©2010 Lewis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lewis, Paul D
Lewis, Keir E
Ghosal, Robin
Bayliss, Sion
Lloyd, Amanda J
Wills, John
Godfrey, Ruth
Kloer, Philip
Mur, Luis AJ
Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum
title Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum
title_full Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum
title_fullStr Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum
title_full_unstemmed Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum
title_short Evaluation of FTIR Spectroscopy as a diagnostic tool for lung cancer using sputum
title_sort evaluation of ftir spectroscopy as a diagnostic tool for lung cancer using sputum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000851/
https://www.ncbi.nlm.nih.gov/pubmed/21092279
http://dx.doi.org/10.1186/1471-2407-10-640
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