| Literature DB >> 28898697 |
Michelle Vaz1, Stephen Y Hwang1, Ioannis Kagiampakis1, Jillian Phallen1, Ashwini Patil2, Heather M O'Hagan3, Lauren Murphy1, Cynthia A Zahnow1, Edward Gabrielson4, Victor E Velculescu1, Hariharan P Easwaran5, Stephen B Baylin6.
Abstract
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.Entities:
Keywords: DNA methylation; HBECs; Kras; addiction; cigarette smoke exposure; epigenetic; genetic; human bronchial epithelial cells; lung cancer; oncogene; polycomb
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Year: 2017 PMID: 28898697 PMCID: PMC5596892 DOI: 10.1016/j.ccell.2017.08.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743