化学
前列腺癌
谷氨酸羧肽酶Ⅱ
药品
癌症研究
抗体-药物偶联物
抗原
药理学
癌症
临床试验
内化
抗体
内科学
医学
单克隆抗体
免疫学
受体
作者
Yousef Mirzaei,Ali Hussein Mer,Bahia Fattah Maran,Leila Omidvar,Fatemeh Misamogooe,Zahra Amirkhani,Nafiseh Javaheri Haghighi,Nader Bagheri,Zahra Keshtkaran,Behzad Rezaei,Farshad Bargrizaneh,Saeed Jahandideh,Nesa Barpour,Hosein Shahsavarani,Ahmadreza Bazyari,Meghdad Abdollahpour‐Alitappeh
标识
DOI:10.1016/j.bioorg.2024.107803
摘要
Prostate-specific membrane antigen (PSMA) is a type II membrane glycoprotein overexpressed in a variety of tumors, especially in nearly all prostate cancers, which makes it a potentially attractive antigen for targeted cancer therapies. More importantly, PSMA, due to no shedding into circulation and efficient internalization after antibody binding, becomes a potential target for antibody-drug conjugates (ADCs), a valid and emerging paradigm of cancer treatment. Four and eight PSMA-directed ADCs have been or are currently being investigated in clinical trials (three of which failed to confirm the promising results while one is currently being evaluated in an ongoing clinical study) and preclinical studies, respectively, for the treatment of PSMA-positive solid tumors, especially prostate cancer. The present study aims to completely review clinical- and preclinical-stage PSMA-directed ADCs.
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