CXCL10型
吲哚胺2,3-双加氧酶
药理学
癌症研究
免疫系统
癌细胞
结直肠癌
癌症
化学
趋化因子
医学
免疫学
内科学
色氨酸
生物化学
氨基酸
作者
Mengdi Yang,Mengran Cao,Xin Zhang,Bin Fu,Yaxin Chen,Yingying Tan,Chenyuan Xuan,Yongren Su,Dashan Tan,Rong Hu
标识
DOI:10.1016/j.biopha.2024.117412
摘要
Indoleamine 2,3-dioxygenase 1 (IDO1) is an immune checkpoint that degrades L-tryptophan to kynurenine (Kyn) and enhance immunosuppression, which can be an attractive target for treating colon cancer. IDO1 inhibitors have limited efficacy when used as monotherapies, and their combination approach has been shown to provide synergistic benefits. Many studies have shown that targeting chemokines can promote the efficacy of immune checkpoint inhibitors. Therefore, this study explored the use of IDO1 inhibitors with multiple chemokines to develop a new combination regimen for IDO1 inhibitors. We found that IDO1 inhibitors reduce the secretion of C-X-C motif ligand 10(CXCL10) in cancer cells, and CXCL10 supplementation significantly improved the anticancer effect of IDO1 inhibitors. The combination of the IDO1 inhibitor with CXCL10 or its agonist axitinib had a synergistic inhibitory effect on the growth of colon cancer cells and transplanted CT26 tumors. This synergistic effect may be achieved by inhibiting cancer cell proliferation, promoting cancer cell apoptosis, promoting CD8
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