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龙血竭提取物通过 METTL3-m6A-Survivin 轴发挥抗 HCC 作用。

Resina Draconis extract exerts anti-HCC effects through METTL3-m6A-Survivin axis.

机构信息

Department of Radiology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.

出版信息

Phytother Res. 2022 Jun;36(6):2542-2557. doi: 10.1002/ptr.7467. Epub 2022 Apr 20.

DOI:10.1002/ptr.7467
PMID:35443090
Abstract

Hepatocellular carcinoma (HCC) is one of the most common malignant tumors worldwide. Herbal medicines have become an important treasure reservoir for anti-HCC drugs because of their high efficiency and low toxicity. Herein, we investigated whether a 75% ethanol extract from Resina Draconis (ERD) exhibited comprehensive anti-HCC effects both in vivo and in vitro. We revealed that ERD effectively inhibited proliferation and triggered apoptosis of HCC cells in a dose- and time-dependent maner, posing no apparent apoptotic toxicity to normal liver cells. Moreover, ERD significantly inhibited the migration, invasion and metastasis of HCC cells. Importantly, ERD treatment effectively inhibited the growth of xenograft HCC in nude mice with low toxicity and low side effects. Molecular mechanism analysis showed that ERD strongly reduced the expression of anti-apoptotic protein Survivin, ultimately leading to the cleavage activation of apoptosis executive proteins such as Caspase 3 and Poly (ADP-ribose) polymerase (PARP). Survivin gene silencing apparently sensitized the apoptotic effect induced by ERD. Further experiments revealed that ERD inhibited N6-methyladenosine (m A) modification in Survivin mRNA by downregulating Methyltransferase-like 3 (METTL3) expression and reducing the binding rate of METTL3 and Survivin mRNA. Together, our findings suggest that ERD can be severed as a novel anti-HCC natural product by targeting METTL3-m A-Survivin axis.

摘要

肝细胞癌(HCC)是全球最常见的恶性肿瘤之一。由于草药的高效低毒,它们已成为抗 HCC 药物的重要宝库。在此,我们研究了从龙血竭(Resina Draconis)中提取的 75%乙醇提取物(ERD)是否在体内和体外均具有全面的抗 HCC 作用。我们揭示 ERD 能有效抑制 HCC 细胞的增殖并诱导其凋亡,且对正常肝细胞没有明显的凋亡毒性。此外,ERD 还能显著抑制 HCC 细胞的迁移、侵袭和转移。重要的是,ERD 治疗能有效抑制裸鼠异种移植 HCC 的生长,且毒性低、副作用小。分子机制分析表明,ERD 能强烈降低抗凋亡蛋白 Survivin 的表达,最终导致凋亡执行蛋白如 Caspase 3 和多聚(ADP-核糖)聚合酶(PARP)的切割激活。Survivin 基因沉默明显增强了 ERD 诱导的凋亡作用。进一步的实验表明,ERD 通过下调甲基转移酶样 3(METTL3)的表达和降低 METTL3 与 Survivin mRNA 的结合率,抑制 Survivin mRNA 的 N6-甲基腺苷(m A)修饰。总之,我们的研究结果表明,ERD 可以通过靶向 METTL3-m A-Survivin 轴,作为一种新型的抗 HCC 天然产物。

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