School of Dentistry, Chung Shan Medical University, Taichung 402, Taiwan.
Molecules. 2013 Feb 26;18(3):2539-48. doi: 10.3390/molecules18032539.
Methyl antcinate A (MAA) is an ergostane-type triterpenoid extracted from the fruiting bodies of Antrodia camphorate that has been reported to be a cytotoxic agent towards some types of cancer cells, such as oral cancer and liver cancer. Cancer stem cells (CSCs) are a particular population within cancer cells which are responsible for tumor initiation, drug resistance and metastasis and targeting CSCs is an emerging area in cancer therapy. In this study, we examine the effect of MAA on cancer stem-like cells in the MCF7 human breast cancer cell line. Although MAA displayed very low cytotoxic effect towards MCF7 under normal culture conditions, it did show good inhibitory effects on the self-renewal capability which was examined by mammosphere culture including primary and secondary sphere. MAA also inhibited cell migration ability of MCF7 sphere cells. By western blot analysis, MAA was shown to suppress the expression of heat shock protein 27 and increase the expression of IkBα and p53. In conclusion, our data demonstrate that MAA has anti-CSC activity and is worthy of future development of potent anticancer agents.
甲基安替比林 A(MAA)是从樟芝的子实体中提取的一种麦角甾烷型三萜类化合物,据报道它是一种对某些类型的癌细胞具有细胞毒性的物质,例如口腔癌和肝癌。癌症干细胞(CSC)是癌细胞中负责肿瘤起始、耐药和转移的特定群体,针对 CSC 是癌症治疗中的一个新兴领域。在这项研究中,我们研究了 MAA 对 MCF7 人乳腺癌细胞系中的癌症干细胞样细胞的影响。尽管 MAA 在正常培养条件下对 MCF7 表现出非常低的细胞毒性作用,但它确实显示出对自我更新能力的良好抑制作用,这通过包括原发性和次级球体的乳腺球体培养来检测。MAA 还抑制 MCF7 球体细胞的迁移能力。通过 Western blot 分析,发现 MAA 抑制热休克蛋白 27 的表达并增加 IkBα 和 p53 的表达。总之,我们的数据表明 MAA 具有抗 CSC 活性,值得进一步开发有效的抗癌药物。