Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore (Singapore).
NUS Graduate School of Integrative Sciences and Engineering, 28 Medical Drive, Singapore (Singapore).
Angew Chem Int Ed Engl. 2015 May 26;54(22):6483-7. doi: 10.1002/anie.201500934. Epub 2015 Apr 14.
There is compelling evidence suggesting that the immune-modulating effects of many conventional chemotherapeutics, including platinum-based agents, play a crucial role in achieving clinical response. One way in which chemotherapeutics can engage a tumor-specific immune response is by triggering an immunogenic mode of tumor cell death (ICD), which then acts as an "anticancer vaccine". In spite of being a mainstay of chemotherapy, there has not been a systematic attempt to screen both existing and upcoming Pt agents for their ICD ability. A library of chemotherapeutically active Pt agents was evaluated in an in vitro phagocytosis assay, and no correlation between cytotoxicity and phagocytosis was observed. A Pt(II) N-heterocyclic carbene complex was found to display the characteristic hallmarks of a type II ICD inducer, namely focused oxidative endoplasmic reticulum (ER) stress, calreticulin exposure, and both HMGB1 and ATP release, and thus identified as the first small-molecule immuno-chemotherapeutic agent.
有确凿的证据表明,许多传统化疗药物(包括铂类药物)的免疫调节作用对临床反应的产生起着至关重要的作用。化疗药物可以通过触发肿瘤细胞死亡的免疫原性模式(ICD)来引发肿瘤特异性免疫反应,从而起到“抗癌疫苗”的作用。尽管铂类药物是化疗的主要药物,但尚未系统地尝试筛选现有和即将推出的铂类药物的 ICD 能力。在体外吞噬测定中评估了一组具有化疗活性的铂类药物库,未观察到细胞毒性与吞噬作用之间存在相关性。发现一种 Pt(II) 氮杂环卡宾配合物具有典型的 II 型 ICD 诱导剂特征,即集中的氧化内质网(ER)应激、钙网蛋白暴露以及 HMGB1 和 ATP 的释放,并因此被鉴定为首个小分子免疫化疗药物。