免疫组织化学
甲状腺癌
药品
甲状腺间变性癌
抗体
体外
药理学
抗体-药物偶联物
癌症研究
甲状腺
医学
结合
甲状腺癌
化学
内科学
病理
免疫学
单克隆抗体
生物化学
数学分析
数学
作者
Peng Zhang,Changjuan Tao,Takaya Shimura,Andrew C. Huang,Nana Kong,Yujie Dai,Shili Yao,Yun Xi,Xing Wang,Jianmin Fang,Marsha A. Moses,Peng Guo
出处
期刊:iScience
[Cell Press]
日期:2023-07-03
卷期号:26 (8): 107272-107272
被引量:11
标识
DOI:10.1016/j.isci.2023.107272
摘要
Treatment options for anaplastic thyroid cancer (ATC) and refractory papillary thyroid carcinoma (PTC) are limited and outcomes remain poor. In this study, we determined via bioinformatic expression analyses and immunohistochemistry staining that intercellular adhesion molecule-1(ICAM1) is an attractive target for ATC and PTC. We designed and engineered two ICAM1-directed antibody-drug conjugate (I1-MMAE and I1-DXd), both of which potently and selectively ablate multiple human ATC and PTC cell lines without affecting non-plastic cells in vitro. Furthermore, I1-MMAE and I1-DXd mediated a potent tumor regression in ATC and PTC xenograft models. To develop a precision medicine, we also explored magnetic resonance imaging (MRI) as a non-invasive biomarker detection method to quantitatively map ICAM1 antigen expression in heterogeneous thyroid tumors. Taken together, this study provides a strong rationale for the further development of I1-MMAE and I1-DXd as promising therapeutic candidates to treat advanced PTC and ATC.
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