Effects of RING-SH2Grb2, a Chimeric Protein Containing the E3 Ligase Domain of Cbl, on the EGFR Pathway

被引:2
|
作者
Lee, Wei-Hao [1 ]
Wang, Pei-Yu [2 ,3 ]
Lin, Yu-Hung [1 ]
Chou, He-Yen [1 ]
Lee, Yen-Hsien [2 ]
Lee, Chien-Kuo [4 ]
Pai, Li-Mei [1 ,2 ,3 ]
机构
[1] Chang Gung Univ, Coll Med, Grad Inst Biomed Sci, Taoyuan 33302, Taiwan
[2] Chang Gung Univ, Dept Biochem, Taoyuan 33302, Taiwan
[3] Chang Gung Univ, Mol Med Res Ctr, Taoyuan 33302, Taiwan
[4] Natl Taiwan Univ, Grad Inst Immunol, Coll Med, Taipei 10051, Taiwan
来源
CHINESE JOURNAL OF PHYSIOLOGY | 2014年 / 57卷 / 06期
关键词
c-Cbl; EGFR; Grb2; lung cancer; RING domain; GROWTH-FACTOR RECEPTOR; UBIQUITIN LIGASES; RING DOMAIN; C-CBL; ENDOCYTOSIS; UBIQUITYLATION; CANCER; LOOPS;
D O I
10.4077/CJP.2014.BAD281
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The E3 ubiquitin-protein ligase Casitas B-lineage lymphoma protein (Cbl) negatively regulates epidermal growth factor receptor (EGFR) signaling pathway in many organisms, and has crucial roles in cell growth, development and human pathologies, including lung cancers. RING-SH2(Grb2) a chimeric protein of 215 amino acids containing the RING domain of Cbl that provides E3 ligase activity, and the SH2 domain of Grb2 that serves as an adaptor for EGFR. In this study, we demonstrated that RING-SH2(Grb2) could promote the ubiquitinylation and degradation of EGFR in a human non-small cell lung carcinoma cell line H1299. Moreover, we discovered that the RING-SH2(Grb2) chimera promoted the internalization of ligand-bound EGFR, inhibited the growth of H1299 cells, and significantly suppressed tumor growth in a xenograft mouse model. In summary, our results revealed a potential new cancer therapeutic approach for non-small cell lung cancer.
引用
收藏
页码:350 / 357
页数:8
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