TY - JOUR
T1 - Effects of RING-SH2 Grb2 , a chimeric protein containing the E3 ligase domain of Cbl, on the EGFR pathway
AU - Lee, Wei Hao
AU - Wang, Pei Yu
AU - Lin, Yu Hung
AU - Chou, He Yen
AU - Lee, Yen Hsien
AU - Lee, Chien Kuo
AU - Pai, Li Mei
N1 - Publisher Copyright:
© 2014 by The Chinese Physiological Society and Airiti Press Inc.
PY - 2014
Y1 - 2014
N2 - 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.
AB - 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.
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U2 - 10.4077/CJP.2014.BAD281
DO - 10.4077/CJP.2014.BAD281
M3 - Article
C2 - 25575524
AN - SCOPUS:84922247893
SN - 0304-4920
VL - 57
SP - 350
EP - 357
JO - Chinese Journal of Physiology
JF - Chinese Journal of Physiology
IS - 6
ER -