多重耐药
抗体-药物偶联物
拓扑异构酶
癌症研究
癌症
药理学
医学
抗药性
体外
生物
抗体
单克隆抗体
内科学
免疫学
生物化学
微生物学
作者
Rui Wang,Peng Fang,Xi Chen,Jiali Ji,Dongan Yu,Fuyang Mei,Zhenzhen Wang,Wei Zhou,Wenjing Peng,Rongjuan Wang,Jian Wang,Cuicui Guo,Hai Wu,Datao Liu,Xiaoding Tan,Xun Gui
标识
DOI:10.1016/j.xcrm.2025.102213
摘要
Cadherin 17 (CDH17) has emerged as a promising target for gastrointestinal (GI) cancers, which are often complicated by multidrug resistance (MDR) and recurrence. In this study, we developed 7MW4911, a CDH17-targeted antibody-drug conjugate (ADC) that incorporates a topoisomerase inhibitor MF-6 (Topi MF-6) payload linked via a cleavable linker, designed specifically to address MDR in GI cancers. 7MW4911 exhibited high specificity for CDH17-expressing cancer cells and potent cytotoxicity in vitro. In preclinical models, including patient-derived xenografts (PDXs) with distinct mutations, 7MW4911 achieved tumor growth inhibition ranging from 71% to 99%. Remarkably, 7MW4911 outperformed monomethyl auristatin E (MMAE)-based and Deruxtecan (DXd)-based ADCs in MDR models, highlighting its effectiveness against drug-resistant cancer phenotypes. Additionally, 7MW4911 showed favorable pharmacokinetics and a highest non-severely toxic dose (HNSTD) exceeding 20 mg/kg in cynomolgus monkeys, underscoring its promising safety profile. Together, these findings position 7MW4911 as a promising ADC candidate capable of enhancing therapeutic outcomes in GI cancers.
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