Centre for Atherothrombotic and Metabolic Disease, Hull York Medical School, University of Hull, Hull, UK.
Histol Histopathol. 2020 Oct;35(10):1059-1075. doi: 10.14670/HH-18-221. Epub 2020 Apr 23.
The transmembrane oncoprotein HER2 is encoded by ERBB2 gene and overexpressed in around 20% of invasive breast cancers. It can be specifically targeted by Trastuzumab (Herceptin®), a humanised IgG1 antibody. Trastuzumab has been regarded as one of the most effective therapeutic drugs targeted to HER2 positive cancers. However, there are drawbacks, notably cardiotoxicity and resistance, which have raised awareness in clinical use. Therefore, understanding the mechanism of action is vital to establish improved therapeutic strategies. Here we evaluate Trastuzumab application in the treatment of HER2 positive breast cancer, focusing on its mechanistic actions and clinical effectiveness. Alternative therapies targeting the HER2 receptor and its downstream anomalies will also be discussed, as these could highlight further targets that could be key to improving clinical outcomes.
跨膜癌蛋白 HER2 由 ERBB2 基因编码,在大约 20%的浸润性乳腺癌中过度表达。它可以被曲妥珠单抗(赫赛汀®)特异性靶向,曲妥珠单抗是一种人源化 IgG1 抗体。曲妥珠单抗已被认为是针对 HER2 阳性癌症最有效的治疗药物之一。然而,它也存在一些缺点,特别是心脏毒性和耐药性,这在临床应用中引起了人们的关注。因此,了解其作用机制对于制定改进的治疗策略至关重要。本文评估了曲妥珠单抗在治疗 HER2 阳性乳腺癌中的应用,重点介绍了其作用机制和临床疗效。还讨论了针对 HER2 受体及其下游异常的替代治疗方法,因为这些方法可能会突出进一步的靶点,这些靶点可能是改善临床结果的关键。