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特发性肺纤维化相关的肺癌发病机制的研究进展

Idiopathic pulmonary fibrosis (IPF) is the most common interstitial lung disease (ILD) of unknown causes, which is characterized by pulmonary fibrosis. The median survival period after diagnosis is about 2-4 years. In recent years, the incidence rate of lung cancer associated with IPF (IPF-LC) is in...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720683/
https://www.ncbi.nlm.nih.gov/pubmed/36419395
http://dx.doi.org/10.3779/j.issn.1009-3419.2022.101.51
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description Idiopathic pulmonary fibrosis (IPF) is the most common interstitial lung disease (ILD) of unknown causes, which is characterized by pulmonary fibrosis. The median survival period after diagnosis is about 2-4 years. In recent years, the incidence rate of lung cancer associated with IPF (IPF-LC) is increasing, and the prognosis is worse than that of IPF alone. Pulmonary fibrosis may be closely associated with the occurrence and development of lung cancer. Although the pathogenesis of IPF-LC is still unclear, the current research shows that there are similarities between the pathogenesis of these two diseases at molecular and cellular levels. At present, the research on the cellular and molecular mechanism of lung cancer related to pulmonary fibrosis has become the focus of researchers' attention. This article reviews the related literature, focusing on the latest status of the cellular and molecular mechanisms and treatment of IPF-LC, hoping to help clinicians understand IPF-LC.
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spelling pubmed-97206832022-12-22 特发性肺纤维化相关的肺癌发病机制的研究进展 Zhongguo Fei Ai Za Zhi 综述 Idiopathic pulmonary fibrosis (IPF) is the most common interstitial lung disease (ILD) of unknown causes, which is characterized by pulmonary fibrosis. The median survival period after diagnosis is about 2-4 years. In recent years, the incidence rate of lung cancer associated with IPF (IPF-LC) is increasing, and the prognosis is worse than that of IPF alone. Pulmonary fibrosis may be closely associated with the occurrence and development of lung cancer. Although the pathogenesis of IPF-LC is still unclear, the current research shows that there are similarities between the pathogenesis of these two diseases at molecular and cellular levels. At present, the research on the cellular and molecular mechanism of lung cancer related to pulmonary fibrosis has become the focus of researchers' attention. This article reviews the related literature, focusing on the latest status of the cellular and molecular mechanisms and treatment of IPF-LC, hoping to help clinicians understand IPF-LC. 中国肺癌杂志编辑部 2022-11-20 /pmc/articles/PMC9720683/ /pubmed/36419395 http://dx.doi.org/10.3779/j.issn.1009-3419.2022.101.51 Text en 版权所有©《中国肺癌杂志》编辑部2022 https://creativecommons.org/licenses/by/3.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/.
spellingShingle 综述
特发性肺纤维化相关的肺癌发病机制的研究进展
title 特发性肺纤维化相关的肺癌发病机制的研究进展
title_full 特发性肺纤维化相关的肺癌发病机制的研究进展
title_fullStr 特发性肺纤维化相关的肺癌发病机制的研究进展
title_full_unstemmed 特发性肺纤维化相关的肺癌发病机制的研究进展
title_short 特发性肺纤维化相关的肺癌发病机制的研究进展
title_sort 特发性肺纤维化相关的肺癌发病机制的研究进展
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720683/
https://www.ncbi.nlm.nih.gov/pubmed/36419395
http://dx.doi.org/10.3779/j.issn.1009-3419.2022.101.51
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