Nahta Rita
Departments of Pharmacology, Hematology and Medical Oncology, School of Medicine; Winship Cancer Institute; Molecular and Systems Pharmacology Program, Graduate Division of Biological and Biomedical Sciences, Emory University, Suite 5001, 1510 Clifton Road, Atlanta, GA 30322, USA.
Chemother Res Pract. 2012;2012:648965. doi: 10.1155/2012/648965. Epub 2012 Jul 9.
Resistance to the HER2-targeted antibody trastuzumab is a major clinical concern in the treatment of HER2-overexpressing metastatic breast cancer. Increased expression or signaling of the insulin-like growth factor-I receptor (IGF-IR) has been reported in a subset of cell lines and clinical samples derived from trastuzumab-resistant breast cancers. Genetic and pharmacologic inhibition of IGF-IR signaling has been shown to improve response to trastuzumab in trastuzumab-naïve and trastuzumab-resistant models. In this paper, we will discuss the role of IGF-IR signaling in trastuzumab resistance. Further, we will discuss cotargeting IGF-IR and HER2 as a potential therapeutic strategy for HER2-over-expressing breast cancers that have progressed on trastuzumab treatment.
对HER2靶向抗体曲妥珠单抗产生耐药性是HER2过表达转移性乳腺癌治疗中的一个主要临床问题。在源自曲妥珠单抗耐药乳腺癌的一部分细胞系和临床样本中,已报道胰岛素样生长因子-I受体(IGF-IR)的表达或信号传导增加。在未经曲妥珠单抗治疗和曲妥珠单抗耐药的模型中,IGF-IR信号传导的基因和药物抑制已显示可改善对曲妥珠单抗的反应。在本文中,我们将讨论IGF-IR信号传导在曲妥珠单抗耐药中的作用。此外,我们将讨论联合靶向IGF-IR和HER2作为曲妥珠单抗治疗后进展的HER2过表达乳腺癌的一种潜在治疗策略。