EGF receptor

被引:893
作者
Wells, A [1 ]
机构
[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[2] Birmingham VAMC, Pathol Serv, Birmingham, AL 35294 USA
[3] Birmingham VAMC, Lab Serv, Birmingham, AL 35294 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
receptor protein tyrosine kinase (RPTK); tumor invasion; wound healing; organogenesis; signaling pathways;
D O I
10.1016/S1357-2725(99)00015-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The receptor for the epidermal growth factor (EGF) and related ligands (EGFR), the prototypal member of the superfamily of receptors with intrinsic tyrosine kinase activity, is widely expressed on many cell types, including epithelial and mesenchymal lineages. Upon activation by at least five genetically distinct ligands (including EGF, transforming growth factor-alpha (TGF alpha) and heparin-binding EGF (HB-EGF)), the intrinsic kinase is activated and EGFR tyrosyl-phosphorylates itself and numerous intermediary effector molecules, including closely-related c-erbB receptor family members. This initiates myriad signaling pathways, some of which attenuate receptor signaling. The integrated biological responses to EGFR signaling are pleiotropic including mitogenesis or apoptosis, enhanced cell motility, protein secretion, and differentiation or dedifferentiation. In addition to being implicated in organ morphogenesis, maintenance and repair, upregulated EGFR signaling has been correlated in a wide variety of tumors with progression to invasion and metastasis. Thus, EGFR and its downstream signaling molecules are targets for therapeutic interventions in wound repair and cancer. Published by Elsevier Science Ltd.
引用
收藏
页码:637 / 643
页数:7
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