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含 TDO 抑制剂的 Pt(IV) 配合物可作为潜在的抗癌免疫调节剂。

Pt(IV) hybrids containing a TDO inhibitor serve as potential anticancer immunomodulators.

机构信息

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.

出版信息

J Inorg Biochem. 2019 Jun;195:130-140. doi: 10.1016/j.jinorgbio.2019.02.004. Epub 2019 Feb 12.

Abstract

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).

摘要

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。

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