Center for Integrated Protein Science Munich CIPSM, Department of Chemistry, Institute of Advanced Studies IAS, Technische Universität München, Lichtenbergstrasse 4, 85747 Garching (Germany); Current address: Department of Oncology/Pathology, Cancer Proteomics Mass Spectrometry, SciLifeLab Stockholm, Karolinska Institutet, Tomtebodavägen 23, 17165 Solna (Sweden).
Angew Chem Int Ed Engl. 2014 Nov 17;53(47):12960-5. doi: 10.1002/anie.201406577. Epub 2014 Sep 26.
Resistance to chemotherapeutic agents represents a major challenge in cancer research. One approach to this problem is combination therapy, the application of a toxic chemotherapeutic drug together with a sensitizing compound that addresses the vulnerability of cancer cells to induce apoptosis. Here we report the discovery of a new compound class (T8) that sensitizes various cancer cells towards etoposide treatment at subtoxic concentrations. Proteomic analysis revealed protein disulfide isomerase (PDI) as the target of the T8 class. In-depth chemical and biological studies such as the synthesis of optimized compounds, molecular docking analyses, cellular imaging, and apoptosis assays confirmed the unique mode of action through reversible PDI inhibition.
耐药性是癌症研究中的一个主要挑战。解决这个问题的一种方法是联合治疗,即将一种有毒的化疗药物与一种增敏化合物联合应用,以利用癌细胞对凋亡的敏感性。在这里,我们报告了一类新的化合物(T8)的发现,它可以在亚毒性浓度下使各种癌细胞对依托泊苷治疗敏感。蛋白质组学分析显示,蛋白二硫键异构酶(PDI)是 T8 类化合物的靶标。通过合成优化化合物、分子对接分析、细胞成像和凋亡分析等深入的化学和生物学研究,证实了通过可逆的 PDI 抑制来实现独特的作用模式。