Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, Shanghai, China.
Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Biochem Pharmacol. 2023 Dec;218:115868. doi: 10.1016/j.bcp.2023.115868. Epub 2023 Oct 21.
Inosine monophosphate dehydrogenase (IMPDH) catalyzes the rate-limiting reaction in the de novo synthesis pathway of guanine nucleotides that is highly required for cancer cell outgrowth. Herein, we found that IMPDH isoform 2 (IMPDH2) is highly expressed in colorectal cancer (CRC) and is correlated with poor patient prognosis. Via structure-based virtual screening, we identified berberrubine, a critical ingredient of the medical plant Coptis chinensis, as a novel, selective, and competitive inhibitor of IMPDH2, which demonstrated over 15-fold selectivity to IMPDH2 than IMPDH1. Besides, we also confirmed the interaction between berberrubine and IMPDH2. Of note, berberrubine treatment significantly impairs the growth of human CRC cells in a dose-dependent manner, which can be rescued by supplementing with guanosine. Furthermore, oral administration of berberrubine remarkably reduced tumor volume and weight in a human cell line-derived xenograft model. Importantly, the anti-cancer activity of berberrubine was also confirmed by using the azoxymethane (AOM) / dextran sulfate sodium (DSS)-induced spontaneous CRC mouse model. Taken together, our study highlights that berberrubine acts as a novel IMPDH2 inhibitor, suppressing the growth of CRC in vitro and in vivo, providing a fresh perspective for its potential application in the treatment of CRC.
肌苷单磷酸脱氢酶(IMPDH)催化从头合成途径中鸟嘌呤核苷酸合成的限速反应,这是癌细胞生长所高度需要的。在此,我们发现肌苷单磷酸脱氢酶同工酶 2(IMPDH2)在结直肠癌(CRC)中高度表达,并与患者预后不良相关。通过基于结构的虚拟筛选,我们发现小檗红碱,一种药用植物黄连的重要成分,是 IMPDH2 的新型、选择性和竞争性抑制剂,对 IMPDH2 的选择性比 IMPDH1 高 15 倍以上。此外,我们还证实了小檗红碱与 IMPDH2 的相互作用。值得注意的是,小檗红碱处理以剂量依赖性方式显著损害人 CRC 细胞的生长,而用鸟苷补充可以挽救这种损害。此外,小檗红碱的口服给药在人细胞系衍生的异种移植模型中显著减少了肿瘤体积和重量。重要的是,小檗红碱的抗癌活性也通过使用氧化偶氮甲烷(AOM)/葡聚糖硫酸钠(DSS)诱导的自发性 CRC 小鼠模型得到了证实。总之,我们的研究强调了小檗红碱作为一种新型的 IMPDH2 抑制剂的作用,抑制 CRC 在体外和体内的生长,为其在 CRC 治疗中的潜在应用提供了新的视角。