Vaz Michelle, Hwang Stephen Y, Kagiampakis Ioannis, Phallen Jillian, Patil Ashwini, O'Hagan Heather M, Murphy Lauren, Zahnow Cynthia A, Gabrielson Edward, Velculescu Victor E, Easwaran Hariharan P, Baylin Stephen B
Department of Oncology, The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Krieger School of Arts and Sciences, Baltimore, MD 21218, USA.
Cancer Cell. 2017 Sep 11;32(3):360-376.e6. doi: 10.1016/j.ccell.2017.08.006.
We define how chronic cigarette smoke-induced time-dependent epigenetic alterations can sensitize human bronchial epithelial cells for transformation by a single oncogene. The smoke-induced chromatin changes include initial repressive polycomb marking of genes, later manifesting abnormal DNA methylation by 10 months. At this time, cells exhibit epithelial-to-mesenchymal changes, anchorage-independent growth, and upregulated RAS/MAPK signaling with silencing of hypermethylated genes, which normally inhibit these pathways and are associated with smoking-related non-small cell lung cancer. These cells, in the absence of any driver gene mutations, now transform by introducing a single KRAS mutation and form adenosquamous lung carcinomas in mice. Thus, epigenetic abnormalities may prime for changing oncogene senescence to addiction for a single key oncogene involved in lung cancer initiation.
我们定义了慢性香烟烟雾诱导的时间依赖性表观遗传改变如何使人类支气管上皮细胞对单一癌基因介导的转化敏感。烟雾诱导的染色质变化包括基因最初的抑制性多梳标记,10个月后表现为异常的DNA甲基化。此时,细胞表现出上皮-间质转化、不依赖贴壁生长,以及RAS/MAPK信号上调,同时高甲基化基因沉默,这些基因通常抑制这些信号通路,并与吸烟相关的非小细胞肺癌有关。在没有任何驱动基因突变的情况下,这些细胞通过引入单个KRAS突变而发生转化,并在小鼠体内形成腺鳞癌。因此,表观遗传异常可能促使参与肺癌发生的单个关键癌基因从衰老转变为成瘾状态。