Karamouzis Michalis V, Badra Filitsa A, Papavassiliou Athanasios G
Department of Biological Chemistry, Medical School, University of Athens, 75, M. Asias Street, 11527 Athens, Greece.
Int J Biochem Cell Biol. 2007;39(5):851-6. doi: 10.1016/j.biocel.2006.11.017. Epub 2006 Dec 27.
Breast cancer is the most common cancer in women and the ErbB receptor family holds crucial role in its pathogenesis. Among them, epidermal growth factor receptor and HER-2 are the most studied members and their overexpression has been associated with aggressive clinical behaviour. These data were further strengthened by the clinical success of trastuzumab, a monoclonal antibody against HER-2 in breast cancer patients with HER-2 overexpression and/or amplification. However, trastuzumab failure in some patients may partly be attributed to co-expression of other ErbB receptors. Herein, we provide updated views regarding the role of HER-3 and HER-4 in breast cancer. Accumulated evidence implies that these receptors should be considered more than heterodimerisation partners. Their expression profile might be useful in predicting responsiveness to current treatment options, while new strategies targeting their ligands and downstream effectors are being developed.
乳腺癌是女性中最常见的癌症,而表皮生长因子受体(ErbB)家族在其发病机制中起着关键作用。其中,表皮生长因子受体(EGFR)和人表皮生长因子受体2(HER-2)是研究最多的成员,它们的过表达与侵袭性临床行为相关。针对HER-2过表达和/或扩增的乳腺癌患者,抗HER-2单克隆抗体曲妥珠单抗在临床上取得的成功进一步证实了这些数据。然而,曲妥珠单抗在一些患者中失效可能部分归因于其他ErbB受体的共表达。在此,我们提供了关于HER-3和HER-4在乳腺癌中作用的最新观点。越来越多的证据表明,这些受体不应仅仅被视为异二聚体伙伴。它们的表达谱可能有助于预测对当前治疗方案的反应性,同时针对其配体和下游效应器的新策略也正在开发中。