Department of Pathology, Queen Elizabeth II Health Sciences Centre and Dalhousie University, Halifax, Nova Scotia, Canada.
J Thorac Dis. 2010 Mar;2(1):48-51.
Epidermal growth factor receptor is a trans-membrane glycoprotein with an extracellular epidermal growth factor binding domain and an intracellular tyrosine kinase domain that regulates signaling pathways to control cellular proliferation. Epidermal growth factor receptor binding to its ligand results in autophosphorylation by intrinsic tyrosine/kinase activity, triggering several signal transduction cascades. Constitutive or sustained activation of these sequences of downstream targets is thought to yield more aggressive tumor phenotypes. Mutations in epidermal growth factor receptor have been discovered in association with some lung cancers. Lung adenocarcinomas with mutated epidermal growth factor receptor have significant responses to tyrosine kinase inhibitors, although for unselected patients it does not appear to have a survival benefit. However, in a subset of patients (non-smoking Asian women with adenocarcinoma, particularly with a bronchioloalveolar carcinoma), there appears to be a significant survival advantage. Both EGFR mutation and gene amplification status may be important in determining which tumors will respond to tyrosine kinase inhibitors.
表皮生长因子受体是一种跨膜糖蛋白,具有细胞外表皮生长因子结合域和细胞内酪氨酸激酶域,可调节信号通路以控制细胞增殖。表皮生长因子受体与其配体结合会导致内在的酪氨酸/激酶活性的自身磷酸化,触发几个信号转导级联反应。这些下游靶标的组成型或持续激活被认为产生更具侵袭性的肿瘤表型。已发现表皮生长因子受体中的突变与一些肺癌有关。具有表皮生长因子受体突变的肺腺癌对酪氨酸激酶抑制剂有显著的反应,尽管对于未选择的患者,它似乎没有生存获益。然而,在一部分患者(非吸烟的亚洲女性的腺癌,特别是细支气管肺泡癌)中,似乎有显著的生存优势。表皮生长因子受体的突变和基因扩增状态可能在决定哪些肿瘤对酪氨酸激酶抑制剂有反应方面很重要。