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表皮生长因子受体

EGF receptor.

作者信息

Wells A

机构信息

Department of Pathology, University of Alabama, Birmingham 35294-0007, USA.

出版信息

Int J Biochem Cell Biol. 1999 Jun;31(6):637-43. doi: 10.1016/s1357-2725(99)00015-1.

Abstract

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.

摘要

表皮生长因子(EGF)及相关配体的受体(EGFR)是具有内在酪氨酸激酶活性的受体超家族的原型成员,在包括上皮和间充质谱系在内的多种细胞类型上广泛表达。在被至少五种基因上不同的配体(包括EGF、转化生长因子-α(TGFα)和肝素结合EGF(HB-EGF))激活后,内在激酶被激活,EGFR自身酪氨酸磷酸化,并使众多中间效应分子酪氨酸磷酸化,这些分子包括密切相关的c-erbB受体家族成员。这启动了无数信号通路,其中一些会减弱受体信号。对EGFR信号的综合生物学反应具有多效性,包括有丝分裂或凋亡、增强细胞运动性、蛋白质分泌以及分化或去分化。除了参与器官形态发生、维持和修复外,EGFR信号上调在多种肿瘤中还与进展至侵袭和转移相关。因此,EGFR及其下游信号分子是伤口修复和癌症治疗干预的靶点。

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