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The Kinome of Human Alveolar Type II and Basal Cells, and Its Reprogramming in Lung Cancer.

Sonia M LeachJay FiniganVihas T VasuRangnath MishraMoumita GhoshDaniel FosterRobert MasonBeata KosmiderEveline Farias HessonJeffrey A Kern
Published in: American journal of respiratory cell and molecular biology (2020)
The discovery of mutant tyrosine kinases as oncogenic drivers of lung adenocarcinomas has changed the basic understanding of lung cancer development and therapy. Yet, expressed kinases (kinome) in lung cancer progenitor cells, as well as whether kinase expression and the overall kinome changes or is reprogrammed upon transformation, is incompletely understood. We hypothesized that the kinome differs between lung cancer progenitor cells, alveolar type II cells (ATII), and basal cells (BC) and that their respective kinomes undergo distinct lineage-specific reprogramming to adenocarcinomas and squamous cell carcinomas upon transformation. We performed RNA sequencing on freshly isolated human ATII, BC, and lung cancer cell lines to define the kinome in nontransformed cells and transformed cells. Our studies identified a unique kinome for ATII and BC and changes in their kinome upon transformation to their respective carcinomas.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • endothelial cells
  • endoplasmic reticulum stress
  • oxidative stress
  • small molecule
  • stem cells
  • cell proliferation
  • high throughput
  • tyrosine kinase
  • protein kinase
  • cell fate