Department of Otolaryngology, Mackay Memorial Hospital, Taipei, Taiwan, ROC.
Department of Medical Research and Department of Radiation Oncology, Mackay Memorial Hospital, Taipei, Taiwan, ROC.
Am J Chin Med. 2019;47(6):1365-1380. doi: 10.1142/S0192415X19500708. Epub 2019 Sep 5.
The honey mushroom, , is known to have medicinal qualities and has been used in recent years as a health food and dietary supplement worldwide. In Asia, it is commonly consumed as an herbal medicine, being a key component of the Chinese preparation "Tien-ma". Here, we examined the antitumor effects of armillaridin, a bioactive compound isolated from , on human hepatocellular carcinoma (HCC) cells. Armillaridin inhibited the growth of human Huh7, HepG2, and HA22T HCC cells, and its cytotoxicity was confirmed by observations of its induction of mitochondrial transmembrane potential collapse. However, armillaridin treatment did not result in large numbers of cells with fragmented chromosomal DNA, suggesting that apoptosis was not responsible for these effects. We therefore tested for signs of autophagic cell death following armillaridin administration. Armillaridin induced LC3 aggregation in green fluorescent protein-LC3-overexpressing cells. Moreover, flow cytometry and immunoblotting revealed that it increased the number of acridine orange-positive cells and upregulated autophagy-related proteins, respectively. Furthermore, armillaridin cytotoxicity was suppressed by the autophagy inhibitor 3-methyladenine. In summary, our results indicated that armillaridin induces HCC cell death by autophagy, and demonstrated the potential of armillaridin as an antihepatoma agent.
蜜环菌,,被认为具有药用价值,近年来已作为一种健康食品和膳食补充剂在全球范围内使用。在亚洲,它通常被用作草药,是中药“天麻”的主要成分之一。在这里,我们研究了从蜜环菌中分离得到的生物活性化合物——armillaridin 对人肝癌(HCC)细胞的抗肿瘤作用。Armillaridin 抑制了人 Huh7、HepG2 和 HA22T HCC 细胞的生长,其诱导线粒体跨膜电位崩溃的观察证实了其细胞毒性。然而,armillaridin 处理并没有导致大量染色体 DNA 片段化的细胞,这表明细胞凋亡不是这些作用的原因。因此,我们检测了 armillaridin 给药后自噬细胞死亡的迹象。Armillaridin 在绿色荧光蛋白-LC3 过表达细胞中诱导 LC3 聚集。此外,流式细胞术和免疫印迹分析显示,它分别增加了吖啶橙阳性细胞的数量和上调了自噬相关蛋白。此外,自噬抑制剂 3-甲基腺嘌呤抑制了 armillaridin 的细胞毒性。综上所述,我们的结果表明,armillaridin 通过自噬诱导 HCC 细胞死亡,并证明了 armillaridin 作为一种抗肝癌药物的潜力。