Targeting STING to promote antitumor immunity

被引:74
作者
Chin, Emily N. [1 ]
Sulpizio, Ariana [1 ]
Lairson, Luke L. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
5,6-DIMETHYLXANTHENONE-4-ACETIC ACID DMXAA; CYCLIC DI-GMP; R71H-G230A-R293Q HUMAN TMEM173; I INTERFERON; ACTIVATION; POTENT; CELLS; RECOGNITION; METASTASIS; SIGNALS;
D O I
10.1016/j.tcb.2022.06.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pharmacology-based methods that promote antitumor immunity have the potential to be highly efficacious while avoiding the systemic cytotoxicity associ-ated with traditional chemotherapies. Activation of type I interferon (IFN) signal-ing in antigen-presenting cell types [e.g., macrophages and dendritic cells (DCs)] is critical, if not essential, for inducing a tumor-specific adaptive immune response, including the activation of cytolytic CD8 T cells. In the context of pro-moting antitumor immunity, the cyclic GMP-AMP synthase/stimulator of IFN genes (cGAS/STING) pathway has emerged as a principal regulator of essential type I IFN signaling. As such, STING represents a highly attractive target for de-veloping a first-in-class immunotherapy, albeit one with a potential for significant cell type-and downstream pathway-dependent on-target toxicities, as well as conceivable pharmacogenomic liabilities.
引用
收藏
页码:189 / 203
页数:15
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