p19ras Represses proliferation of non-small cell lung cancer possibly through interaction with Neuron-Specific Enolase (NSE)

被引:15
作者
Jang, Sang-Min [1 ]
Kim, Jung-Woong [1 ]
Kim, Chul-Hong [1 ]
Kim, Daehwan [1 ]
Rhee, Sangmyung [1 ]
Choi, Kyung-Hee [1 ]
机构
[1] Chung Ang Univ, Coll Nat Sci, Dept Life Sci, Program BK21, Seoul 156756, South Korea
关键词
p19(ras); Neuron-Specific Enolase (NSE); Glycolytic enzyme; Protein-protein interaction; Non-small cell lung cancer; SERUM TUMOR-MARKERS; GLYCOLYTIC-ENZYMES; PROTEIN; EXPRESSION; APOPTOSIS; REGION; GENES; ROLES; YEAST;
D O I
10.1016/j.canlet.2009.08.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
p19(ras) is an alternative splicing product of the proto-oncogene c-H-ras pre-mRNA. In this study, we identified a novel p19(ras)-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 p19(ras) and NSE via co-immunoprecipitation assay. We also identified the interaction region of p19(ras), which is required for binding with NSE. When full-length p19(ras) and C-terminal region are bound to NSE, it inhibits the enzymatic activity of NSE. Furthermore, p19(ras) interacted with Enolase alpha (Eno alpha) and repressed its enzymatic activity in vitro. p19(ras) repressed lung cancer cell proliferation mostly increased by NSE in H1299 cells. Taken together, these results suggest that p19(ras) is a novel regulator to suppress cell proliferation in lung cancer through the interaction with NSE. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:91 / 98
页数:8
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