NHC Key Laboratory of Biotechnology of Antibiotics, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1 Tiantan Xili, Beijing 100050, China.
Department of Organic Chemistry, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1 Tiantan Xili, Beijing 100050, China.
J Med Chem. 2023 Nov 9;66(21):14700-14715. doi: 10.1021/acs.jmedchem.3c01210. Epub 2023 Oct 26.
Herein, we first prepared a novel anti-TROP2 antibody-drug conjugate (ADC) hIMB1636-MMAE using hIMB1636 antibody chemically coupled to monomethyl auristatin E (MMAE) via a Valine-Citrulline linker and then reported its characteristics and antitumor activity. With a DAR of 3.92, it binds specifically to both recombinant antigen ( ∼ 0.687 nM) and cancer cells and could be internalized by target cells and selectively kill them with IC values at nanomolar/subnanomolar levels by inducing apoptosis and G2/M phase arrest. hIMB1636-MMAE also inhibited cell migration, induced ADCC effects, and had bystander effects. It displayed significant tumor-targeting ability and excellent tumor-suppressive effects in vivo, resulting in 5/8 tumor elimination at 12 mg/kg in the T3M4 xenograft model or complete tumor disappearance at 10 mg/kg in BxPc-3 xenografts in nude mice. Its half-life in mice was about 87 h. These data suggested that hIMB1636-MMAE was a promising candidate for the treatment of pancreatic cancer with TROP2 overexpression.
在此,我们首次使用通过缬氨酸-瓜氨酸接头化学偶联至单甲基澳瑞他汀 E(MMAE)的 hIMB1636 抗体,制备了一种新型的抗 TROP2 抗体药物偶联物(ADC)hIMB1636-MMAE。随后报告了其特性和抗肿瘤活性。该 ADC 的药物抗体比(DAR)为 3.92,它可特异性结合重组抗原(∼0.687 nM)和癌细胞,并可通过诱导细胞凋亡和 G2/M 期阻滞,以纳摩尔/亚纳摩尔级别的 IC 值被靶细胞内化并选择性杀死它们。hIMB1636-MMAE 还抑制细胞迁移,诱导 ADCC 效应,并具有旁观者效应。它在体内显示出显著的肿瘤靶向能力和优异的肿瘤抑制作用,在 T3M4 异种移植模型中,以 12 mg/kg 的剂量可消除 5/8 的肿瘤,或以 10 mg/kg 的剂量在裸鼠的 BxPc-3 异种移植中可完全消除肿瘤。其在小鼠体内的半衰期约为 87 h。这些数据表明,hIMB1636-MMAE 是一种很有前途的用于治疗 TROP2 过表达的胰腺癌的候选药物。