Department of Pathology, Genentech, San Francisco, CA, USA.
Max Planck Institute, Munich, Germany.
J Exp Clin Cancer Res. 2018 Feb 6;37(1):20. doi: 10.1186/s13046-017-0667-1.
Antibody-Drug Conjugates (ADCs) are a class of cancer therapeutics that combines antigen specificity and potent cytotoxicity in a single molecule as they are comprised of an engineered antibody linked chemically to a cytotoxic drug. Four ADCs have received approval by the Food and Drug Administration (FDA) and the European Medicine Agency (EMA) and can be prescribed for metastatic conditions while around 60 ADCs are currently enrolled in clinical trials. The efficacy of an ADC greatly relies on its intracellular trafficking and processing of its components to trigger tumor cell death. A limited number of studies have addressed these critical processes that both challenge and help foster the design of ADCs. This review highlights those mechanisms and their relevance for future development of ADCs as cancer therapeutics.
抗体药物偶联物(ADCs)是一类癌症治疗药物,它将抗原特异性和强大的细胞毒性结合在一个单一的分子中,因为它由一个经过工程改造的抗体通过化学连接到一个细胞毒性药物上。四种 ADC 已获得美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)的批准,并可用于治疗转移性疾病,而目前约有 60 种 ADC 正在进行临床试验。ADC 的疗效在很大程度上依赖于其细胞内运输和成分的加工,以触发肿瘤细胞死亡。少数研究已经解决了这些具有挑战性的过程,这些过程有助于促进 ADC 的设计。这篇综述强调了这些机制及其对未来 ADC 作为癌症治疗药物的发展的相关性。