Department of Neurological Surgery, Northwestern University, Chicago, USA.
Department of Pediatrics, Northwestern University, Chicago, USA.
Cell Mol Immunol. 2018 May;15(5):447-457. doi: 10.1038/cmi.2017.143. Epub 2018 Jan 29.
Indoleamine 2, 3-dioxygenase 1 (IDO1) is a rate-limiting metabolic enzyme that converts the essential amino acid tryptophan (Trp) into downstream catabolites known as kynurenines. Coincidently, numerous studies have demonstrated that IDO1 is highly expressed in multiple types of human cancer. Preclinical studies have further introduced an interesting paradox: while single-agent treatment with IDO1 enzyme inhibitor has a negligible effect on decreasing the established cancer burden, approaches combining select therapies with IDO1 blockade tend to yield a synergistic benefit against tumor growth and/or animal subject survival. Given the high expression of IDO1 among multiple cancer types along with the lack of monotherapeutic efficacy, these data suggest that there is a more complex mechanism of action than previously appreciated. Similar to the dual faces of the astrological Gemini, we highlight the multiple roles of IDO1 and review its canonical association with IDO1-dependent tryptophan metabolism, as well as documented evidence confirming the dispensability of enzyme activity for its immunosuppressive effects. The gene transcript levels for IDO1 highlight its strong association with T-cell infiltration, but the lack of a universal prognostic significance among all cancer subtypes. Finally, ongoing clinical trials are discussed with consideration of IDO1-targeting strategies that enhance the efficacy of immunotherapy for cancer patients.
吲哚胺 2,3-双加氧酶 1(IDO1)是一种限速代谢酶,可将必需氨基酸色氨酸(Trp)转化为下游代谢产物犬尿氨酸。巧合的是,大量研究表明 IDO1 在多种人类癌症中高度表达。临床前研究进一步引入了一个有趣的悖论:虽然单独使用 IDO1 酶抑制剂治疗对减少已建立的癌症负担几乎没有影响,但将选择性治疗方法与 IDO1 阻断相结合的方法往往会对肿瘤生长和/或动物存活产生协同益处。鉴于 IDO1 在多种癌症类型中的高表达以及单一疗法疗效的缺乏,这些数据表明存在比以前认识到的更复杂的作用机制。类似于占星术中的双子座的两面性,我们强调了 IDO1 的多种作用,并回顾了其与 IDO1 依赖性色氨酸代谢的经典关联,以及证实酶活性对其免疫抑制作用的非必要性的已有证据。IDO1 的基因转录水平突出了其与 T 细胞浸润的强烈关联,但并非所有癌症亚型都具有普遍的预后意义。最后,讨论了正在进行的临床试验,并考虑了针对 IDO1 的靶向策略,以提高癌症患者免疫疗法的疗效。