RMC-7977(AbMole,M54858)是一种广谱、高选择性的RAS (ON)多选择性抑制剂,RMC-7977的核心作用机制是靶向RAS蛋白的GTP结合活性状态(即RAS[ON]构象),能同时抑制突变型和野生型KRAS、NRAS及HRAS的活性,从而阻断下游MAPK信号通路(RAS-RAF-MEK-ERK)的持续激活。在多种肿瘤模型中,RMC-7977通过抑制RAS信号传导,诱导细胞周期阻滞和凋亡。例如,在KRAS突变型结直肠癌细胞中,RMC-7977能有效阻断ERK磷酸化,抑制增殖并诱导部分细胞的凋亡。值得注意的是,RMC-7977还能重塑肿瘤免疫微环境。在PDAC和黑色素瘤模型中,RMC-7977(CAS No.:2765082-12-8)能减少免疫抑制性髓系细胞的浸润,同时增加CD4+和CD8+ T细胞以及常规树突状细胞的浸润,从而触发免疫系统介导的肿瘤消退。
参考文献
Popescu, B.; Jones, M. F.; Piao, M.; et al. Multiselective RAS(ON) inhibition targets oncogenic RAS and overcomes RAS-mediated resistance to FLT3i and BCL2i in AML. Blood 2026, 147 (3), 276-289.
Anastacio Da Costa Carvalho, L.; Tovbis Shifrin, N.; Phadke, M. S.; et al. RAS(ON) Multiselective Inhibition Drives Antitumor Immunity in Preclinical Models of NRAS-Mutant Melanoma. Cancer immunology research 2026, 14 (1), 90-106.
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