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鉴定 m6A 天然抑制剂洛贝林可逆转肝癌对仑伐替尼的耐药性。

Identification of an m6A Natural Inhibitor, Lobeline, That Reverses Lenvatinib Resistance in Hepatocellular Tumors.

机构信息

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.

出版信息

J Nat Prod. 2024 Aug 23;87(8):1983-1993. doi: 10.1021/acs.jnatprod.4c00406. Epub 2024 Aug 13.

Abstract

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.

摘要

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。

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