| Literature DB >> 23857717 |
Renat Shaykhiev1, Rui Wang, Rachel K Zwick, Neil R Hackett, Roland Leung, Malcolm A S Moore, Camelia S Sima, Ion Wa Chao, Robert J Downey, Yael Strulovici-Barel, Jacqueline Salit, Ronald G Crystal.
Abstract
Activation of the human embryonic stem cell (hESC) signature genes has been observed in various epithelial cancers. In this study, we found that the hESC signature is selectively induced in the airway basal stem/progenitor cell population of healthy smokers (BC-S), with a pattern similar to that activated in all major types of human lung cancer. We further identified a subset of 6 BC-S hESC genes, whose coherent overexpression in lung adenocarcinoma (AdCa) was associated with reduced lung function, poorer differentiation grade, more advanced tumor stage, remarkably shorter survival, and higher frequency of TP53 mutations. BC-S shared with hESC and a considerable subset of lung carcinomas a common TP53 inactivation molecular pattern which strongly correlated with the BC-S hESC gene expression. These data provide transcriptome-based evidence that smoking-induced reprogramming of airway BC toward the hESC-like phenotype might represent a common early molecular event in the development of aggressive lung carcinomas in humans. © AlphaMed Press.Entities:
Keywords: Airway epithelium; Basal cells; Gene expression; Lung cancer; Stem cells
Mesh:
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Year: 2013 PMID: 23857717 PMCID: PMC4051142 DOI: 10.1002/stem.1459
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277