Britten Carolyn D
Division of Hematology/Oncology, Department of Medicine, David Geffen School of Medicine at University of California at Los Angeles, 10945 Le Conte Avenue, Los Angeles, CA 90095, USA.
Mol Cancer Ther. 2004 Oct;3(10):1335-42.
The ErbB receptors are localized to the cell membrane where they are activated by ligand to trigger a network of signaling pathways. In some cancer cells, dysregulation of ErbB-mediated signaling confers a growth advantage, resulting in cellular transformation and increased metastatic potential. Several agents that inhibit individual ErbB receptors have recently been approved for the treatment of human malignancies, validating ErbB receptors as therapeutic targets. One strategy to improve the efficacy of ErbB-targeted therapies is to inhibit multiple ErbB receptors, thereby interfering with the cooperation that exists between receptors. This minireview addresses the approaches being developed to concurrently inhibit multiple ErbB receptors.
表皮生长因子受体(ErbB)定位于细胞膜,在那里它们被配体激活,从而触发信号通路网络。在一些癌细胞中,ErbB介导的信号失调赋予了生长优势,导致细胞转化和转移潜能增加。最近,几种抑制单个ErbB受体的药物已被批准用于治疗人类恶性肿瘤,这证实了ErbB受体是治疗靶点。提高ErbB靶向治疗疗效的一种策略是抑制多个ErbB受体,从而干扰受体之间存在的协同作用。这篇迷你综述讨论了正在开发的同时抑制多个ErbB受体的方法。