Institute of Marine Biology and Pharmacology, Ocean College, Zhejiang University, Zhoushan 316021, China.
Key Laboratory of Digestive Pathophysiology of Zhejiang Province, the First Affiliated Hospital of Zhejiang Chinese Medicine, First Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310053, China.
J Med Chem. 2024 Aug 8;67(15):13446-13473. doi: 10.1021/acs.jmedchem.4c01323. Epub 2024 Jul 25.
Based on the structure of caerulomycin A, 90 novel bipyridine derivatives were designed and synthesized. Among these, compound exerted strong antitumor effects in vivo and in vitro. Importantly, NOP2/Sun RNA methyltransferase 3 (NSUN3) protein was identified as the target specific binding to , which inhibits oxidative phosphorylation of mitochondrial energy metabolism and enhances glycolytic activity by binding to NSUN3. Knockdown of inhibited both proliferation and migration of colorectal cancer (CRC) cells by activating AMPK-related signaling and inhibiting downstream STAT3 signaling to exert antiproliferative and pro-apoptotic effects. Our findings support the use of NSUN3 inhibitors as promising therapeutic strategies against CRC.
基于卡泊霉素 A 的结构,设计并合成了 90 种新型联吡啶衍生物。其中,化合物 在体内和体外均表现出很强的抗肿瘤作用。重要的是,NOP2/Sun RNA 甲基转移酶 3(NSUN3)蛋白被鉴定为与 特异性结合的靶标,通过与 NSUN3 结合抑制线粒体能量代谢的氧化磷酸化并增强糖酵解活性。抑制 可通过激活 AMPK 相关信号通路和抑制下游 STAT3 信号通路来抑制结直肠癌细胞(CRC)的增殖和迁移,从而发挥抗增殖和促凋亡作用。我们的研究结果支持将 NSUN3 抑制剂作为治疗 CRC 的有前途的治疗策略。