创新链/学科链/研发链/产业链

新药研发前沿动态 / 医药领域趋势进展

叶科, 邱亚涛, 张婉衡, 蒋晟. 吲哚胺2,3-双加氧酶-1及其抑制剂的研究进展[J]. 药学进展, 2019, 43(7): 483-503.
引用本文: 叶科, 邱亚涛, 张婉衡, 蒋晟. 吲哚胺2,3-双加氧酶-1及其抑制剂的研究进展[J]. 药学进展, 2019, 43(7): 483-503.
YE Ke, QIU Yatao, ZHANG Wanheng, JIANG Sheng. Research Advances of Indoleamine 2, 3-Dioxygenase-1 and Its Inhibitors[J]. Progress in Pharmaceutical Sciences, 2019, 43(7): 483-503.
Citation: YE Ke, QIU Yatao, ZHANG Wanheng, JIANG Sheng. Research Advances of Indoleamine 2, 3-Dioxygenase-1 and Its Inhibitors[J]. Progress in Pharmaceutical Sciences, 2019, 43(7): 483-503.

吲哚胺2,3-双加氧酶-1及其抑制剂的研究进展

Research Advances of Indoleamine 2, 3-Dioxygenase-1 and Its Inhibitors

  • 摘要: 吲哚胺2, 3-双加氧酶-1是色氨酸通过犬尿氨酸途径代谢的一种关键限速酶。其在多种肿瘤细胞中高表达,介导肿瘤免疫逃逸,与肿瘤的恶性转化以及病人预后差等密切相关。吲哚胺2, 3-双加氧酶-1已经成为潜在的肿瘤免疫治疗药物靶点。目前已有许多不同结构的吲哚胺2, 3-双加氧酶-1抑制剂被报道,其中多个抑制剂已进入临床研究阶段。综述吲哚胺2, 3-双加氧酶-1在肿瘤免疫逃逸中的作用机制以及相关药物研究最新进展,旨在为肿瘤免疫疗法提供新思路。

     

    Abstract: Indoleamine 2, 3-dioxygenase-1 (IDO1) is a key rate-limiting metabolic enzyme which catalyzes the degradation of the essential amino acid tryptophan along the kynurenine pathway. It participates in tumor immune escape and has been found to be overexpressed in various cancer types, which is closely associated with the malignant transformation of tumors and the poor prognosis of cancer patients. IDO1 has emerged as a promising target for immunotherapeutic agents against tumors. To date, a number of structurally diversified IDO1 inhibitors have been reported, with quite a few having entered clinical trials. This paper summarizes the recent progress in the study of the mechanisms of action of IDO1 in tumor immune escape and its related drugs, so as to provide new ideas for tumor immunotherapy.

     

/

返回文章
返回