作者
Thomas D. Aicher,Chad A. Van Huis,Alexander R. Hurd,Donald J. Skalitzky,Clarke Taylor,Omar M Beleh,Gary D. Glick,Peter L. Toogood,Bing Yang,Tao Zheng,Chang‐Xin Huo,Jie Gao,Chenxi Qiao,Xiaolong Tian,Junping Zhang,Kellie Demock,Ling-Yang Hao,Charles Lesch,Rodney Morgan,Jacques Moisan,Yahong Wang,JoAnn Scatina,Chrystal M. Paulos,Weiping Zou,Laura Carter,Xiao Hu
摘要
Retinoic acid receptor-related orphan receptor γ (RORc, RORγ, or NR1F3) is the nuclear receptor master transcription factor that drives the function and development of IL-17-producing T helper cells (Th17), cytotoxic T cells (Tc17), and subsets of innate lymphoid cells. Activation of RORγ+ T cells in the tumor microenvironment is hypothesized to render immune infiltrates more effective at countering tumor growth. To test this hypothesis, a family of benzoxazines was optimized to provide LYC-55716 (37c), a potent, selective, and orally bioavailable small-molecule RORγ agonist. LYC-55716 decreases tumor growth and enhances survival in preclinical tumor models and was nominated as a clinical development candidate for evaluation in patients with solid tumors.