Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2114135 | Cancer Letters | 2010 | 8 Pages |
p19ras is an alternative splicing product of the proto-oncogene c-H-ras pre-mRNA. In this study, we identified a novel p19ras-binding protein, Neuron-Specific Enolase (NSE), using the yeast two-hybrid method. NSE is one of the enolase families that convert 2-phospho-d-glycerate (PGA) to phosphoenolpyruvate (PEP) in the glycolysis pathway. In both endogenous and over-expressed systems, we confirmed interactions between p19ras and NSE via co-immunoprecipitation assay. We also identified the interaction region of p19ras, which is required for binding with NSE. When full-length p19ras and C-terminal region are bound to NSE, it inhibits the enzymatic activity of NSE. Furthermore, p19ras interacted with Enolase α (Enoα) and repressed its enzymatic activity in vitro. p19ras repressed lung cancer cell proliferation mostly increased by NSE in H1299 cells. Taken together, these results suggest that p19ras is a novel regulator to suppress cell proliferation in lung cancer through the interaction with NSE.