Cargando…

Lung cancer: a new frontier for microbiome research and clinical translation

The lung microbiome has been shown to reflect a range of pulmonary diseases—for example: asthma, chronic obstructive pulmonary disease (COPD) and cystic fibrosis. Studies have now begun to show microbiological changes in the lung that correlate with lung cancer (LC) which could provide new insights...

Descripción completa

Detalles Bibliográficos
Autores principales: Mur, Luis AJ, Huws, Sharon A, Cameron, Simon JS, Lewis, Paul D, Lewis, Keir E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145518/
https://www.ncbi.nlm.nih.gov/pubmed/30263057
http://dx.doi.org/10.3332/ecancer.2018.866
_version_ 1783356270366949376
author Mur, Luis AJ
Huws, Sharon A
Cameron, Simon JS
Lewis, Paul D
Lewis, Keir E
author_facet Mur, Luis AJ
Huws, Sharon A
Cameron, Simon JS
Lewis, Paul D
Lewis, Keir E
author_sort Mur, Luis AJ
collection PubMed
description The lung microbiome has been shown to reflect a range of pulmonary diseases—for example: asthma, chronic obstructive pulmonary disease (COPD) and cystic fibrosis. Studies have now begun to show microbiological changes in the lung that correlate with lung cancer (LC) which could provide new insights into lung carcinogenesis and new biomarkers for disease screening. Clinical studies have suggested that infections with tuberculosis or pneumonia increased the risk of LC possibly through inflammatory or immunological changes. These have now been superseded by genomic-based microbiome sequencing studies based on bronchoalveolar lavage, sputum or saliva samples. Although some discrepancies exist, many have suggested changes in particular bacterial genera in LC samples particularly, Granulicatella, Streptococcus and Veillonella. Granulicatella is of particular interest, as it appeared to show LC stage-specific increases in abundance. We propose that these microbial community changes are likely to reflect biochemical changes in the LC lung, linked to an increase in anaerobic environmental niches and altered pyridoxal/polyamine/nitrogenous metabolism to which Granulicatella could be particularly responsive. These are clearly preliminary observations and many more expansive studies are required to develop our understanding of the LC microbiome.
format Online
Article
Text
id pubmed-6145518
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Cancer Intelligence
record_format MEDLINE/PubMed
spelling pubmed-61455182018-09-27 Lung cancer: a new frontier for microbiome research and clinical translation Mur, Luis AJ Huws, Sharon A Cameron, Simon JS Lewis, Paul D Lewis, Keir E Ecancermedicalscience Review The lung microbiome has been shown to reflect a range of pulmonary diseases—for example: asthma, chronic obstructive pulmonary disease (COPD) and cystic fibrosis. Studies have now begun to show microbiological changes in the lung that correlate with lung cancer (LC) which could provide new insights into lung carcinogenesis and new biomarkers for disease screening. Clinical studies have suggested that infections with tuberculosis or pneumonia increased the risk of LC possibly through inflammatory or immunological changes. These have now been superseded by genomic-based microbiome sequencing studies based on bronchoalveolar lavage, sputum or saliva samples. Although some discrepancies exist, many have suggested changes in particular bacterial genera in LC samples particularly, Granulicatella, Streptococcus and Veillonella. Granulicatella is of particular interest, as it appeared to show LC stage-specific increases in abundance. We propose that these microbial community changes are likely to reflect biochemical changes in the LC lung, linked to an increase in anaerobic environmental niches and altered pyridoxal/polyamine/nitrogenous metabolism to which Granulicatella could be particularly responsive. These are clearly preliminary observations and many more expansive studies are required to develop our understanding of the LC microbiome. Cancer Intelligence 2018-09-05 /pmc/articles/PMC6145518/ /pubmed/30263057 http://dx.doi.org/10.3332/ecancer.2018.866 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Mur, Luis AJ
Huws, Sharon A
Cameron, Simon JS
Lewis, Paul D
Lewis, Keir E
Lung cancer: a new frontier for microbiome research and clinical translation
title Lung cancer: a new frontier for microbiome research and clinical translation
title_full Lung cancer: a new frontier for microbiome research and clinical translation
title_fullStr Lung cancer: a new frontier for microbiome research and clinical translation
title_full_unstemmed Lung cancer: a new frontier for microbiome research and clinical translation
title_short Lung cancer: a new frontier for microbiome research and clinical translation
title_sort lung cancer: a new frontier for microbiome research and clinical translation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145518/
https://www.ncbi.nlm.nih.gov/pubmed/30263057
http://dx.doi.org/10.3332/ecancer.2018.866
work_keys_str_mv AT murluisaj lungcanceranewfrontierformicrobiomeresearchandclinicaltranslation
AT huwssharona lungcanceranewfrontierformicrobiomeresearchandclinicaltranslation
AT cameronsimonjs lungcanceranewfrontierformicrobiomeresearchandclinicaltranslation
AT lewispauld lungcanceranewfrontierformicrobiomeresearchandclinicaltranslation
AT lewiskeire lungcanceranewfrontierformicrobiomeresearchandclinicaltranslation