Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.
Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China; Jiangsu Province Hi-Tech Key Laboratory for Bio-medical Research, Southeast University, Nanjing 211189, China.
J Inorg Biochem. 2019 Jun;195:130-140. doi: 10.1016/j.jinorgbio.2019.02.004. Epub 2019 Feb 12.
Tryptophan 2,3-dioxygenase (TDO), an immunosuppressive enzyme, can involve in immune evasion and tumor tolerance. TDO inhibitors can boost the efficacy of chemotherapeutics by promoting immunity. Herein, a strategy to introduce a TDO inhibitor into Pt(IV) complexes for reversing tumor immune suppression was adopted. A mono-modified Pt(IV) complex, 3, displayed significant antitumor activity against human liver cancer cells. Flow cytometry study revealed that complex 3 could induce cell death via a mitochondrial-dependent apoptosis pathway and arrest the cell cycle at S phase. Furthermore, complex 3 was effective to enhance T-cell immune responses by inhibiting the TDO enzyme expression to block the kynurenine production and inactivating the downstream of aryl hydrocarbon receptor (AHR).
色氨酸 2,3-双加氧酶(TDO)是一种免疫抑制酶,可参与免疫逃逸和肿瘤耐受。TDO 抑制剂可通过促进免疫来提高化疗药物的疗效。在此,采用了将 TDO 抑制剂引入 Pt(IV) 配合物以逆转肿瘤免疫抑制的策略。单修饰的 Pt(IV)配合物 3 对人肝癌细胞显示出显著的抗肿瘤活性。流式细胞术研究表明,配合物 3 可通过线粒体依赖性凋亡途径诱导细胞死亡,并将细胞周期阻滞在 S 期。此外,通过抑制 TDO 酶的表达来阻断犬尿氨酸的产生并使芳香烃受体(AHR)下游失活,配合物 3 能够有效地增强 T 细胞免疫反应。