Title of article :
p19ras Represses proliferation of non-small cell lung cancer possibly through interaction with Neuron-Specific Enolase (NSE)
Author/Authors :
Jang، نويسنده , , Sang-Min and Kim، نويسنده , , Jung-Woong and Kim، نويسنده , , Chul-Hong and Kim، نويسنده , , Daehwan and Rhee، نويسنده , , Sangmyung and Choi، نويسنده , , Kyung-Hee، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2010
Abstract :
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.
Keywords :
p19ras , glycolytic enzyme , Protein–protein interaction , Non-small cell lung cancer , Neuron-specific enolase (NSE)
Journal title :
Cancer Letters
Journal title :
Cancer Letters