Chen Wei-Lun, Pan Li, Kinghorn A Douglas, Swanson Steven M, Burdette Joanna E
Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, Chicago, IL, 60607, USA.
Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Ohio State University, Columbus, OH, 43210, USA.
BMC Cancer. 2016 Jan 13;16:17. doi: 10.1186/s12885-015-1988-0.
Silvestrol is a cyclopenta[b]benzofuran that was isolated from the fruits and twigs of Aglaia foveolata, a plant indigenous to Borneo in Southeast Asia. The purpose of the current study was to determine if inhibition of protein synthesis caused by silvestrol triggers autophagy and apoptosis in cultured human cancer cells derived from solid tumors.
In vitro cell viability, flow cytometry, fluorescence microscopy, qPCR and immunoblot was used to study the mechanism of action of silvestrol in MDA-MB-435 melanoma cells.
By 24 h, a decrease in cyclin B and cyclin D expression was observed in silvestrol-treated cells relative to control. In addition, silvestrol blocked progression through the cell cycle at the G2-phase. In silvestrol-treated cells, DAPI staining of nuclear chromatin displayed nucleosomal fragments. Annexin V staining demonstrated an increase in apoptotic cells after silvestrol treatment. Silvestrol induced caspase-3 activation and apoptotic cell death in a time- and dose-dependent manner. Furthermore, both silvestrol and SAHA enhanced autophagosome formation in MDA-MB-435 cells. MDA-MB-435 cells responded to silvestrol treatment with accumulation of LC3-II and time-dependent p62 degradation. Bafilomycin A, an autophagy inhibitor, resulted in the accumulation of LC3 in cells treated with silvestrol. Silvestrol-mediated cell death was attenuated in ATG7-null mouse embryonic fibroblasts (MEFs) lacking a functional autophagy protein.
Silvestrol potently inhibits cell growth and induces cell death in human melanoma cells through induction of early autophagy and caspase-mediated apoptosis. Silvestrol represents a natural product scaffold that exhibits potent cytotoxic activity and could be used for the further study of autophagy and its relationship to apoptosis in cancer cells.
西维司特罗是一种环戊二烯并[b]苯并呋喃,从东南亚婆罗洲本土植物凹脉米仔兰的果实和嫩枝中分离得到。本研究的目的是确定西维司特罗引起的蛋白质合成抑制是否会触发源自实体瘤的培养人癌细胞中的自噬和凋亡。
采用体外细胞活力检测、流式细胞术、荧光显微镜、定量聚合酶链反应和免疫印迹法研究西维司特罗在MDA-MB-435黑色素瘤细胞中的作用机制。
至24小时时,与对照组相比,西维司特罗处理的细胞中细胞周期蛋白B和细胞周期蛋白D表达降低。此外,西维司特罗在G2期阻断细胞周期进程。在西维司特罗处理的细胞中,核染色质的4',6-二脒基-2-苯基吲哚(DAPI)染色显示核小体片段。膜联蛋白V染色表明西维司特罗处理后凋亡细胞增加。西维司特罗以时间和剂量依赖性方式诱导半胱天冬酶-3激活和凋亡细胞死亡。此外,西维司特罗和伏立诺他均增强了MDA-MB-435细胞中自噬体的形成。MDA-MB-435细胞对西维司特罗处理的反应是微管相关蛋白1轻链3-II(LC3-II)的积累和p62的时间依赖性降解。自噬抑制剂巴弗洛霉素A导致西维司特罗处理的细胞中LC3积累。在缺乏功能性自噬蛋白的自噬相关基因7(ATG7)缺失的小鼠胚胎成纤维细胞(MEF)中,西维司特罗介导的细胞死亡减弱。
西维司特罗通过诱导早期自噬和半胱天冬酶介导的凋亡,有效抑制人黑色素瘤细胞的生长并诱导其死亡。西维司特罗代表一种具有强大细胞毒活性的天然产物支架,可用于进一步研究自噬及其与癌细胞凋亡的关系。