Department of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China; University of Utah, Department of Pathology and ARUP Laboratories, Salt Lake City, UT, USA.
University of Utah, Department of Pathology and ARUP Laboratories, Salt Lake City, UT, USA; Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Nanomedicine. 2018 Feb;14(2):581-593. doi: 10.1016/j.nano.2017.11.001. Epub 2017 Nov 21.
The finding of HER2 overexpression in osteosarcoma (OS) makes HER2 a potential therapeutic target. However, studies indicate OS cells are nonresponsive to anti-HER2 antibody trastuzumab (TRA) therapy. We established stable, non-covalent association of TRA with nanomaterial graphene oxide (GO) to generated multivalent TRA/GO complexes that demonstrated markedly enhanced HER2-binding activity and capacity to rapidly kill OS cells. TRA/GO simultaneously induced oxidative stress and HER2 signaling in the target cells, leading to rapid depletion of the cellular inhibitors of apoptosis protein (cIAP) and caspase-8, formation of RIP1/RIPK3/MLKL necroptosome and necroptosis of the OS cells. Intravenous administration of TRA/GO eradicated established xenograft the OS in immunodeficient mice, resulting in indefinite survival of the animals, whereas TRA in its original form failed to do so. No appreciable side effects were observed with TRA/GO therapy. The results demonstrate a novel, nontoxic, curative therapy for a HER2 cancer in a preclinical animal model.
骨肉瘤(OS)中 HER2 的过表达的发现使得 HER2 成为潜在的治疗靶点。然而,研究表明 OS 细胞对抗 HER2 抗体曲妥珠单抗(TRA)治疗无反应。我们建立了 TRA 与纳米材料氧化石墨烯(GO)的稳定非共价缔合,生成具有明显增强的 HER2 结合活性和快速杀死 OS 细胞能力的多价 TRA/GO 复合物。TRA/GO 同时诱导靶细胞中的氧化应激和 HER2 信号转导,导致细胞凋亡抑制剂(cIAP)和胱天蛋白酶-8 的迅速耗竭,形成 RIP1/RIPK3/MLKL 坏死小体和 OS 细胞的坏死。静脉注射 TRA/GO 消除了免疫缺陷小鼠中已建立的骨肉瘤异种移植物,导致动物的无限期存活,而原形式的 TRA 则不能。TRA/GO 治疗没有观察到明显的副作用。这些结果表明,在临床前动物模型中,针对 HER2 癌症的一种新型、无毒、治愈性治疗方法。