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Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review
OBJECTIVE: We systematically review the molecular mechanism of the interaction between lung cancer (LC) and tuberculosis (TB), and put forward the existing problems in order to provide suggestions for early intervention and future research direction. BACKGROUND: TB and LC are two global public healt...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577982/ https://www.ncbi.nlm.nih.gov/pubmed/34858788 http://dx.doi.org/10.21037/tlcr-21-465 |
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author | Xiong, Kunlong Sun, Wenwen He, Yayi Fan, Lin |
author_facet | Xiong, Kunlong Sun, Wenwen He, Yayi Fan, Lin |
author_sort | Xiong, Kunlong |
collection | PubMed |
description | OBJECTIVE: We systematically review the molecular mechanism of the interaction between lung cancer (LC) and tuberculosis (TB), and put forward the existing problems in order to provide suggestions for early intervention and future research direction. BACKGROUND: TB and LC are two global public health problems affecting human health. LC is the main cause of cancer-related death worldwide and TB is one of the leading causes of death among infectious diseases, especially in resource-poor areas. Previous studies have suggested that a history of TB may be associated with an increased risk of LC. With the improvement of LC treatment, the occurrence of pulmonary tuberculosis in the course of LC treatment is also frequently reported recently. METHODS: The molecular immunological mechanisms of interaction between LC and TB, and related epidemiological literature are reviewed. The research progress and problems to be solved are summarized. CONCLUSIONS: Chronic inflammation, immune abnormalities, scar formation, gene mutations and drug effects caused by TB may be associated with the occurrence of LC induced by abnormalities in various molecular pathways. LC and decreased immunity during treatment may also increase the risk of latent TB activation or new TB infection through immune pathways. Data on dual burden areas of TB and LC are still lacking, and more clinical studies are needed to elucidate the association. |
format | Online Article Text |
id | pubmed-8577982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-85779822021-12-01 Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review Xiong, Kunlong Sun, Wenwen He, Yayi Fan, Lin Transl Lung Cancer Res Review Article OBJECTIVE: We systematically review the molecular mechanism of the interaction between lung cancer (LC) and tuberculosis (TB), and put forward the existing problems in order to provide suggestions for early intervention and future research direction. BACKGROUND: TB and LC are two global public health problems affecting human health. LC is the main cause of cancer-related death worldwide and TB is one of the leading causes of death among infectious diseases, especially in resource-poor areas. Previous studies have suggested that a history of TB may be associated with an increased risk of LC. With the improvement of LC treatment, the occurrence of pulmonary tuberculosis in the course of LC treatment is also frequently reported recently. METHODS: The molecular immunological mechanisms of interaction between LC and TB, and related epidemiological literature are reviewed. The research progress and problems to be solved are summarized. CONCLUSIONS: Chronic inflammation, immune abnormalities, scar formation, gene mutations and drug effects caused by TB may be associated with the occurrence of LC induced by abnormalities in various molecular pathways. LC and decreased immunity during treatment may also increase the risk of latent TB activation or new TB infection through immune pathways. Data on dual burden areas of TB and LC are still lacking, and more clinical studies are needed to elucidate the association. AME Publishing Company 2021-10 /pmc/articles/PMC8577982/ /pubmed/34858788 http://dx.doi.org/10.21037/tlcr-21-465 Text en 2021 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Article Xiong, Kunlong Sun, Wenwen He, Yayi Fan, Lin Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review |
title | Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review |
title_full | Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review |
title_fullStr | Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review |
title_full_unstemmed | Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review |
title_short | Advances in molecular mechanisms of interaction between Mycobacterium tuberculosis and lung cancer: a narrative review |
title_sort | advances in molecular mechanisms of interaction between mycobacterium tuberculosis and lung cancer: a narrative review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577982/ https://www.ncbi.nlm.nih.gov/pubmed/34858788 http://dx.doi.org/10.21037/tlcr-21-465 |
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