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肺纤维化中的肺癌:上皮细胞可塑性的故事。

Lung cancer in pulmonary fibrosis: tales of epithelial cell plasticity.

机构信息

Comprehensive Pneumology Center, Ludwig Maximilians University, University Hospital Grosshadern, and Helmholtz Zentrum München, Munich, Germany. melanie.koenigshoff @ helmholtz-muenchen.de

出版信息

Respiration. 2011;81(5):353-8. doi: 10.1159/000326299. Epub 2011 Apr 19.

Abstract

Lung epithelial cells exhibit a high degree of plasticity. Alterations to lung epithelial cell function are critically involved in several chronic lung diseases such as pulmonary fibrosis. Pulmonary fibrosis is characterized by repetitive injury and subsequent impaired repair of epithelial cells, which leads to aberrant growth factor activation and fibroblast accumulation. Increased proliferation and hyper- and metaplasia of epithelial cells upon injury have also been observed in pulmonary fibrosis; this epithelial cell activation might represent the basis for lung cancer development. Indeed, several studies have provided histopathological evidence of an increased incidence of lung cancer in pulmonary fibrosis. The mechanisms involved in the development of cancer in pulmonary fibrosis, however, remain poorly understood. This review highlights recently uncovered molecular mechanisms shared between lung cancer and fibrosis, which extend the current evidence of a common trait of cancer and fibrosis, as provided by histopathological observations.

摘要

肺上皮细胞表现出高度的可塑性。肺上皮细胞功能的改变与几种慢性肺部疾病(如肺纤维化)密切相关。肺纤维化的特征是上皮细胞反复损伤和随后的修复受损,导致生长因子异常激活和成纤维细胞积聚。在肺纤维化中也观察到损伤后上皮细胞的增殖增加以及过度和化生;这种上皮细胞激活可能是肺癌发展的基础。事实上,几项研究提供了肺纤维化中肺癌发病率增加的组织病理学证据。然而,肺纤维化中癌症发展所涉及的机制仍知之甚少。本综述强调了最近发现的肺癌和纤维化之间共同的分子机制,这些机制扩展了组织病理学观察所提供的癌症和纤维化的共同特征的现有证据。

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