Division of Respiratory Medicine, Department of Internal Medicine, Nihon University School of Medicine, Tokyo, Japan.
Division of Oncologic Pathology, Department of Pathology and Microbiology, Nihon University School of Medicine, Tokyo, Japan.
Thorac Cancer. 2021 May;12(9):1449-1452. doi: 10.1111/1759-7714.13924. Epub 2021 Mar 30.
Lung cancer (LC) is the most fatal complication of idiopathic pulmonary fibrosis (IPF). However, the molecular pathogenesis of the development of LC from IPF is still unclear. Here, we report a case of IPF-associated LC for which we investigated the genetic alterations between IPF and LC. We extracted formalin-fixed paraffin-embedded DNA from each part of the surgical lung tissue using a laser-assisted microdissection technique. The mutations in each part were detected by next-generation sequencing (NGS) using 72 lung cancer-related mutation panels. Five mutations were found in IPF and four in LC. Almost all somatic mutations did not overlap between the IPF and LC regions. These findings suggest that IPF-associated LC may not be a result of the accumulation of somatic mutations in the regenerated epithelium of the honeycomb lung in the IPF region.
肺癌(LC)是特发性肺纤维化(IPF)最致命的并发症。然而,从 IPF 发展为 LC 的分子发病机制仍不清楚。在这里,我们报告了一例与特发性肺纤维化相关的肺癌,我们研究了 IPF 和 LC 之间的遗传改变。我们使用激光辅助显微切割技术从手术肺组织的每个部分提取福尔马林固定石蜡包埋的 DNA。通过使用 72 个肺癌相关突变面板的下一代测序(NGS)检测每个部分的突变。在 IPF 中发现了 5 个突变,在 LC 中发现了 4 个。几乎所有的体细胞突变在 IPF 和 LC 区域之间都没有重叠。这些发现表明,特发性肺纤维化相关的肺癌可能不是 IPF 区域蜂窝肺再生上皮中体细胞突变积累的结果。