用于治疗结直肠癌肝转移的抗 Claudin-2 抗体-药物共轭物。

IF 5.3 2区 医学 Q1 ONCOLOGY Molecular Cancer Therapeutics Pub Date : 2024-10-01 DOI:10.1158/1535-7163.MCT-23-0393
Sébastien Tabariès, Alma Robert, Anne Marcil, Binbing Ling, Mauro Acchione, Julie Lippens, Martine Pagé, Annie Fortin, Luc Meury, Mathieu Coutu, Matthew G Annis, Charlotte Girondel, Julie Navarre, Maria Jaramillo, Anna N Moraitis, Peter M Siegel
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引用次数: 0

摘要

我们已经证明,Claudin-2 是结直肠癌(CRC)肝转移的必要条件。Claudin-2在原发性结直肠癌中的表达与生存率低有关,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的肝转移。这些观察结果支持将 Claudin-2 作为治疗肝转移患者的潜在治疗靶点。抗体药物共轭物(ADCs)是一种前景广阔的抗肿瘤疗法,它结合了单克隆抗体的特异性靶向能力和细胞毒性药物的强大细胞杀伤活性。在此,我们报告了 28 种抗 Claudin-2 抗体的生成情况,并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跨物种反应性。测试了多种药物共轭物,最后选择了 PNU 与结合细胞外环 1 或细胞外环 2 的抗 Claudin-2 抗体共轭。抗Claudin-2 ADC能在体外有效内化并杀死表达Claudin-2的CRC癌细胞。重要的是,利用已建立的 CRC 细胞系和 CRC 肝转移患者衍生异种移植(PDX)模型,PNU 结合物-抗 Claudin-2 ADCs 在体内可抑制替代型 CRC 肝转移灶的发展。我们的研究结果表明,开发以Claudin-2为靶点的ADCs是治疗出现替代型肝转移的CRC肝转移患者的一种很有前景的治疗策略。
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Anti-Claudin-2 Antibody-Drug Conjugates for the Treatment of Colorectal Cancer Liver Metastasis.

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.

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来源期刊
CiteScore
11.20
自引率
1.80%
发文量
331
审稿时长
3 months
期刊介绍: Molecular Cancer Therapeutics will focus on basic research that has implications for cancer therapeutics in the following areas: Experimental Cancer Therapeutics, Identification of Molecular Targets, Targets for Chemoprevention, New Models, Cancer Chemistry and Drug Discovery, Molecular and Cellular Pharmacology, Molecular Classification of Tumors, and Bioinformatics and Computational Molecular Biology. The journal provides a publication forum for these emerging disciplines that is focused specifically on cancer research. Papers are stringently reviewed and only those that report results of novel, timely, and significant research and meet high standards of scientific merit will be accepted for publication.
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