鉴定可逆转肝细胞肿瘤对伦伐替尼耐药性的 m6A 天然抑制剂 Lobeline。

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2024-08-23 Epub Date: 2024-08-13 DOI:10.1021/acs.jnatprod.4c00406
Lei Zhao, Heyao Ma, Yuhui Jiang, Yingying Li, Li Qiao, Yu Chen, Xiaowen Jiang, Lihui Wang, Shu Wang, Xinyu Fan
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引用次数: 0

摘要

肝细胞癌(HCC)是一种影响人类健康的侵袭性癌症。作为治疗 HCC 的一线药物,来伐替尼(Lenvatinib,Len)尽管疗效显著,但在 HCC 患者中却容易产生耐药性。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耐药性方面也显示出巨大的潜力。我们小组首先利用点印迹技术,从390个化合物(大部分为天然产物)库中筛选出一种小分子m6A调节剂--lobeline(Lob)。体外实验证明,Lob能显著提高对Len耐药的HCC(HCC/Len)对Len的敏感性,并抑制耐药细胞的迁移。在对Len耐药的细胞衍生和患者衍生异种移植模型中,Lob可以逆转耐药表型,使肿瘤体积分别减少68%和60%。此外,MeRIP-m6A测序结果表明,Lob逆转HCC耐药性的分子机制与UBE3B有关。综上所述,本研究强调了植物提取的天然产物 Lob 可通过调节 m6A 水平逆转 HCC 对 Len 的耐药性。希望这能为 HCC 患者的临床治疗提供药理学研究依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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.

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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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