Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, Taichung 40447, Taiwan.
College of Medicine, China Medical University, Taichung 40402, Taiwan.
Mar Drugs. 2021 Apr 26;19(5):244. doi: 10.3390/md19050244.
In this study, the anti-proliferative effect of ilimaquinone, a sesquiterpene derivative from the marine sponge, in breast cancer cells was investigated. Ilimaquinone inhibited the proliferation of MCF-7 and MDA-MB-231 breast cancer cells with IC values of 10.6 μM and 13.5 μM, respectively. Non-tumorigenic human breast epithelial cells were less sensitive to ilimaquinone than breast cancer cells. Flow cytometric and Western blot analysis showed that ilimaquinone induced S-phase arrest by modulating the expression of p-CDC-2 and p21. Ilimaquinone induces apoptosis, which is accompanied by multiple biological biomarkers, including the downregulation of Akt, ERK, and Bax, upregulation of p38, loss of mitochondrial membrane potential, increased reactive oxygen species generation, and induced autophagy. Collectively, these findings suggest that ilimaquinone causes cell cycle arrest as well as induces apoptosis and autophagy in breast cancer cells.
在这项研究中,研究了来自海洋海绵的倍半萜烯衍生物伊莱马醌对乳腺癌细胞的抗增殖作用。伊莱马醌对 MCF-7 和 MDA-MB-231 乳腺癌细胞的增殖具有抑制作用,IC 值分别为 10.6 μM 和 13.5 μM。非致瘤性人乳腺上皮细胞对伊莱马醌的敏感性低于乳腺癌细胞。流式细胞术和 Western blot 分析表明,伊莱马醌通过调节 p-CDC-2 和 p21 的表达诱导 S 期停滞。伊莱马醌诱导细胞凋亡,伴随着多种生物学生物标志物,包括 Akt、ERK 和 Bax 的下调,p38 的上调,线粒体膜电位的丧失,活性氧的产生增加,以及自噬的诱导。综上所述,这些发现表明伊莱马醌导致乳腺癌细胞周期停滞,并诱导细胞凋亡和自噬。