Fabi Alessandra, Mottolese Marcella, Segatto Oreste
Department of Medical Oncology, Regina Elena National Cancer Institute, Rome, Italy.
J Mol Med (Berl). 2014 Jul;92(7):681-95. doi: 10.1007/s00109-014-1169-7. Epub 2014 May 28.
ERBB2 gene amplification occurs in about one quarter of breast carcinomas (BCs) and identifies a distinct clinical subset of BC. The introduction in the clinic of Trastuzumab, a humanized monoclonal antibody (mAb) directed to the ERBB2 extracellular domain, has had a great impact on the therapeutic management of ERBB2+ BC. Yet, not all patients respond to Trastuzumab and resistance develops also among patients that initially benefit from Trastuzumab-based regimens. Pre-clinical studies have discovered several mechanisms through which tumor cells may escape from Trastuzumab-mediated ERBB2 inhibition. These include rewiring of the ErbB signaling network, loss of ERBB2 expression, expression of ERBB2 isoforms refractory to Trastuzumab inhibition, vicarious signaling by non-ErbB tyrosine kinases and constitutive activation of downstream signaling routes, such as the PI3K pathway. While the relative contribution of each of these mechanisms to establishing Trastuzumab resistance in the clinical setting is not fully understood, much attention has been focused on abating resistance by achieving complete blockade of ERBB2-containing dimers. This approach, propelled by the development of novel anti-ERBB2 therapeutics, has led to the recent approval of Lapatinib, Pertuzumab and T-DM1 as additional anti-ERBB2 therapeutics in BC. However, full success is far from being achieved and resistance to ERBB2 targeting remains a relevant problem in the clinical management of BC. Herein, we provide an overview of biological and molecular bases underpinning resistance to ERBB2 therapeutics in BC, discuss outstanding issues in the field of ERBB2 therapeutic targeting and elaborate on future directions of translational research on ERBB2+ breast cancer.
ERBB2基因扩增约见于四分之一的乳腺癌(BC)中,并确定了BC的一个独特临床亚组。针对ERBB2细胞外结构域的人源化单克隆抗体(mAb)曲妥珠单抗应用于临床,对ERBB2阳性BC的治疗管理产生了重大影响。然而,并非所有患者对曲妥珠单抗都有反应,而且在最初受益于基于曲妥珠单抗方案的患者中也会出现耐药。临床前研究已经发现了几种肿瘤细胞可能逃避曲妥珠单抗介导的ERBB2抑制的机制。这些机制包括ErbB信号网络的重新布线、ERBB2表达缺失、对曲妥珠单抗抑制具有抗性的ERBB2异构体的表达、非ErbB酪氨酸激酶的替代信号传导以及下游信号通路(如PI3K通路)的组成性激活。虽然这些机制中的每一种在临床环境中建立曲妥珠单抗耐药性的相对贡献尚未完全了解,但人们已将大量注意力集中在通过完全阻断含ERBB2的二聚体来减轻耐药性上。这种方法在新型抗ERBB2疗法的推动下,导致拉帕替尼、帕妥珠单抗和曲妥珠单抗偶联物(T-DM1)最近被批准作为BC中的额外抗ERBB2疗法。然而,尚未完全取得成功,对ERBB2靶向治疗的耐药性在BC的临床管理中仍然是一个相关问题。在此,我们概述了BC中对ERBB2疗法耐药的生物学和分子基础,讨论了ERBB2治疗靶向领域的突出问题,并阐述了ERBB2阳性乳腺癌转化研究的未来方向。