Anglia Ruskin University, School of Life Science, Faculty of Science and Engineering, East Road, Cambridge, CB1 1PT, UK.
Medannex Ltd, 1 Lochrin Square, 92-98 Fountainbridge, Edinburgh, Scotland, EH3 9QA, UK.
Oncogene. 2024 Feb;43(8):608-614. doi: 10.1038/s41388-023-02919-9. Epub 2024 Jan 10.
In this study we conducted the first investigation to assess the efficacy of a novel therapeutic antibody developed to target annexin-A1 (ANXA1). ANXA1 is an immunomodulatory protein which has been shown to be overexpressed in, and promote the development and progression of, several cancer types. In particular, high ANXA1 expression levels correlate with poorer overall survival in pancreatic and triple-negative breast cancers, two cancers with considerable unmet clinical need. MDX-124 is a humanised IgG1 monoclonal antibody which specifically binds to ANXA1 disrupting its interaction with formyl peptide receptors 1 and 2 (FPR1/2). Here we show that MDX-124 significantly reduced proliferation (p < 0.013) in a dose-dependent manner across a panel of human cancer cell lines expressing ANXA1. The anti-proliferative effect of MDX-124 is instigated by arresting cell cycle progression with cancer cells accumulating in the G phase of the cell cycle. Furthermore, MDX-124 significantly inhibited tumour growth in both the 4T1-luc triple-negative breast and Pan02 pancreatic cancer syngeneic mouse models (p < 0.0001). These findings suggest ANXA1-targeted therapy is a viable and innovative approach to treat tumours which overexpress ANXA1.
在这项研究中,我们首次评估了一种新型治疗性抗体的疗效,该抗体旨在靶向膜联蛋白 A1(ANXA1)。ANXA1 是一种免疫调节蛋白,已被证明在多种癌症中过度表达,并促进其发展和进展。特别是,高 ANXA1 表达水平与胰腺和三阴性乳腺癌的总生存率较差相关,这两种癌症都有相当大的未满足的临床需求。MDX-124 是一种人源化 IgG1 单克隆抗体,特异性结合 ANXA1,从而破坏其与甲酰肽受体 1 和 2(FPR1/2)的相互作用。在这里,我们表明 MDX-124 以剂量依赖性方式显著降低了表达 ANXA1 的一系列人类癌细胞系的增殖(p<0.013)。MDX-124 的抗增殖作用通过将癌细胞在细胞周期的 G 期停滞来引发,从而导致细胞周期进程停滞。此外,MDX-124 显著抑制了 4T1-luc 三阴性乳腺癌和 Pan02 胰腺癌细胞同源小鼠模型中的肿瘤生长(p<0.0001)。这些发现表明,靶向 ANXA1 的治疗是治疗过度表达 ANXA1 的肿瘤的一种可行且创新的方法。