Trassl Lilith, Stathopoulos Georgios T
Institute for Lung Health and Immunity, Helmholtz Munich-German Research Center for Environmental Health, 81377 Munich, Germany.
Munich Medical Research School, Ludwig-Maximilian-University Munich, 81377 Munich, Germany.
Cancers (Basel). 2022 Sep 2;14(17):4303. doi: 10.3390/cancers14174303.
Malignant pleural mesothelioma (MPM) is a rare, incurable cancer of the mesothelial cells lining the lungs and the chest wall that is mainly caused by asbestos inhalation. The molecular mechanisms of mesothelial carcinogenesis are still unclear despite comprehensive studies of the mutational landscape of MPM, and the most frequently mutated genes and cannot cause MPM in mice in a standalone fashion. Although pathway alterations were sporadically detected in older studies employing targeted sequencing, they have been largely undetected by next generation sequencing. We recently identified mutations and copy number alterations in a significant proportion of MPM patients. Here, we review and analyze multiple human datasets and the published literature to show that, in addition to , multiple other genes of the pathway are perturbed in a significant proportion of patients with MPM.
恶性胸膜间皮瘤(MPM)是一种罕见的、无法治愈的癌症,发生于肺和胸壁的间皮细胞,主要由吸入石棉所致。尽管对MPM的突变图谱进行了全面研究,但间皮细胞癌变的分子机制仍不清楚,而且最常发生突变的基因无法单独在小鼠中引发MPM。虽然在早期采用靶向测序的研究中偶尔检测到通路改变,但下一代测序在很大程度上未检测到这些改变。我们最近在相当一部分MPM患者中发现了突变和拷贝数改变。在此,我们回顾并分析了多个人类数据集和已发表的文献,以表明除了[具体基因]外,相当一部分MPM患者中多个其他[具体通路]基因也受到干扰。