Department of Hepatobiliary and Pancreatic Surgery, The First Hospital of China Medical University, Shenyang, Liaoning 110001, China.
Department of Pharmacology, School of Pharmacy, China Medical University, Shenyang, Liaoning 110122, China.
J Nat Prod. 2024 Aug 23;87(8):1983-1993. doi: 10.1021/acs.jnatprod.4c00406. Epub 2024 Aug 13.
Hepatocellular carcinoma (HCC) is an aggressive cancer that has an effect on human health. As a first-line drug for HCC, despite its excellent efficacy, lenvatinib (Len) is prone to developing drug resistance in HCC patients. The N6-methyladenosine (m6A) modification is not only related to the development of HCC but also shows great potential in overcoming HCC resistance. Using Dot Blot, our group first screened a small molecule m6A regulator, lobeline (Lob), from a library of 390 compounds (mostly natural products). In vitro experiments demonstrated that Lob could significantly enhance the sensitivity to Len of Len-resistant HCC (HCC/Len) and inhibit migration of resistant cells. In Len-resistant cell-derived and patient-derived xenograft models, Lob could reverse the resistant phenotype, with reductions in tumor volume of 68% and 60%, respectively. Furthermore, MeRIP-m6A sequencing results indicated that the underlying molecular mechanism of Lob reversal of HCC drug resistance was related to UBE3B. Taken together, this study highlighted that Lob, a plant derived natural product, could reverse the resistance of HCC to Len by regulating the m6A levels. It is hoped that this will provide a pharmacological research basis for the clinical treatment of HCC patients.
肝细胞癌 (HCC) 是一种侵袭性癌症,严重影响人类健康。仑伐替尼 (Len) 作为 HCC 的一线药物,尽管疗效显著,但 HCC 患者容易产生耐药性。N6-甲基腺苷 (m6A) 修饰不仅与 HCC 的发生发展有关,而且在克服 HCC 耐药性方面也具有巨大潜力。本课题组首次利用 Dot Blot 从 390 种化合物库(主要为天然产物)中筛选出小分子 m6A 调节剂洛贝林 (Lob)。体外实验表明,Lob 可显著增强仑伐替尼耐药 HCC(HCC/Len)对仑伐替尼的敏感性,并抑制耐药细胞的迁移。在仑伐替尼耐药细胞衍生的和患者来源的异种移植模型中,Lob 可逆转耐药表型,肿瘤体积分别减少 68%和 60%。此外,MeRIP-m6A 测序结果表明,Lob 逆转 HCC 耐药的潜在分子机制与 UBE3B 有关。综上所述,本研究表明,洛贝林这种植物来源的天然产物可以通过调节 m6A 水平逆转 HCC 对仑伐替尼的耐药性。希望这将为 HCC 患者的临床治疗提供药理学研究基础。