Goodman Cancer Institute, McGill University, Montréal, Canada.
Department of Medicine, McGill University, Montréal, Canada.
Mol Cancer Ther. 2024 Oct 1;23(10):1459-1470. doi: 10.1158/1535-7163.MCT-23-0393.
We have previously demonstrated that Claudin-2 is required for colorectal cancer (CRC) liver metastasis. The expression of Claudin-2 in primary CRC is associated with poor survival and highly expressed in liver metastases. Claudin-2 also promotes breast cancer liver metastasis by enabling seeding and cancer cell survival. These observations support Claudin-2 as a potential therapeutic target for managing patients with liver metastases. Antibody-drug conjugates (ADC) are promising antitumor therapeutics, which combine the specific targeting ability of monoclonal antibodies with the potent cell killing activity of cytotoxic drugs. Herein, we report the generation of 28 anti-Claudin-2 antibodies for which the binding specificities, cross-reactivity with claudin family members, and cross-species reactivity were assessed by flow cytometry analysis. Multiple drug conjugates were tested, and PNU was selected for conjugation with anti-Claudin-2 antibodies binding either extracellular loop 1 or 2. Anti-Claudin-2 ADCs were efficiently internalized and were effective at killing Claudin-2-expressing CRC cancer cells in vitro. Importantly, PNU-conjugated-anti-Claudin-2 ADCs impaired the development of replacement-type CRC liver metastases in vivo, using established CRC cell lines and patient-derived xenograft (PDX) models of CRC liver metastases. Results suggest that the development of ADCs targeting Claudin-2 is a promising therapeutic strategy for managing patients with CRC liver-metastatic disease who present replacement-type liver metastases.
我们之前已经证明 Claudin-2 对于结直肠癌(CRC)肝转移是必需的。原发性 CRC 中 Claudin-2 的表达与不良预后相关,并且在肝转移中高度表达。 Claudin-2 还通过促进播种和癌细胞存活来促进乳腺癌肝转移。这些观察结果支持 Claudin-2 作为管理肝转移患者的潜在治疗靶标。抗体药物偶联物(ADC)是有前途的抗肿瘤治疗药物,它将单克隆抗体的特异性靶向能力与细胞毒性药物的强大细胞杀伤活性结合在一起。在此,我们报告了 28 种抗 Claudin-2 抗体的产生,通过流式细胞术分析评估了这些抗体的结合特异性、与 Claudin 家族成员的交叉反应性以及种间反应性。测试了多种药物偶联物,并且选择 PNU 与结合 Claudin-2 的抗体进行偶联,这些抗体结合在细胞外环 1 或 2 上。抗 Claudin-2 ADC 能够有效内化,并在体外有效杀死表达 Claudin-2 的 CRC 癌细胞。重要的是,PNU 偶联的抗 Claudin-2 ADC 能够损害体内替代型 CRC 肝转移的发展,使用已建立的 CRC 细胞系和 CRC 肝转移的患者来源异种移植(PDX)模型。结果表明,针对 Claudin-2 的 ADC 开发是管理具有替代型肝转移的 CRC 肝转移疾病患者的一种很有前途的治疗策略。