Muller Alexander J, Prendergast George C
Lankenau Institute for Medical Research, Wynnewood, Pennsylvania 19096, USA.
Cancer Res. 2005 Sep 15;65(18):8065-8. doi: 10.1158/0008-5472.CAN-05-2213.
Activation of the tryptophan catabolizing enzyme indoleamine 2,3-dioxygenase (IDO) in cancer cells facilitates immune escape. A recent study now shows how small-molecule inhibitors of IDO can be used to leverage the efficacy of traditional chemotherapeutic drugs that are used to treat cancer in the clinic. By promoting antitumor immune responses in combination with cytotoxic chemotherapy, IDO inhibitors may offer a drug-based strategy to more effectively attack systemic cancer.
癌细胞中色氨酸分解代谢酶吲哚胺2,3-双加氧酶(IDO)的激活促进了免疫逃逸。最近的一项研究表明,IDO小分子抑制剂可用于增强临床上用于治疗癌症的传统化疗药物的疗效。通过与细胞毒性化疗联合促进抗肿瘤免疫反应,IDO抑制剂可能提供一种基于药物的策略来更有效地攻击全身性癌症。