Brochez Lieve, Chevolet Ines, Kruse Vibeke
Department of Dermatology, Ghent University Hospital, Belgium; Dermatology Research Unit, Ghent, Belgium; Immuno-Oncology Network Ghent (ION Ghent), Belgium; Cancer Research Institute Ghent (CRIG), Belgium.
Department of Dermatology, Ghent University Hospital, Belgium; Dermatology Research Unit, Ghent, Belgium; Immuno-Oncology Network Ghent (ION Ghent), Belgium.
Eur J Cancer. 2017 May;76:167-182. doi: 10.1016/j.ejca.2017.01.011. Epub 2017 Mar 18.
Indoleamine 2,3-dioxygenase (IDO, also referred to as IDO1) has been demonstrated to be a normal endogenous mechanism of acquired peripheral immune tolerance in vivo. In the field of oncology, IDO expression and/or activity has been observed in several cancer types and has usually been associated with negative prognostic factors and worse outcome measures. This manuscript reviews current available data on the role of IDO in cancer and the current results obtained with IDO inhibition, both in animal models and in phase 1 and 2 clinical trials in humans. Preliminary results with IDO inhibitors, usually combined with other anti-cancer drugs, seem encouraging. Further studies are needed to clarify the conditions in which IDO inhibitors can be of value as an anti-cancer strategy. In addition, further research should address whether the expression of IDO in tissue or blood can be a marker to select patients who can benefit most from IDO inhibition.
吲哚胺2,3-双加氧酶(IDO,也称为IDO1)已被证明是体内获得性外周免疫耐受的一种正常内源性机制。在肿瘤学领域,已在多种癌症类型中观察到IDO的表达和/或活性,并且通常与负面预后因素和较差的预后指标相关。本文综述了关于IDO在癌症中的作用的现有数据,以及在动物模型和人类1期及2期临床试验中使用IDO抑制剂所获得的当前结果。IDO抑制剂通常与其他抗癌药物联合使用,其初步结果似乎令人鼓舞。需要进一步研究以阐明IDO抑制剂作为抗癌策略有价值的条件。此外,进一步的研究应探讨组织或血液中IDO的表达是否可作为选择最能从IDO抑制中获益的患者的标志物。