Tang Xiang-Jun, Huang Kuan-Ming, Gui Hui, Wang Jun-Jie, Lu Jun-Ti, Dai Long-Jun, Zhang Li, Wang Gang
Department of Neurosurgery, TaiHe Hospital, Hubei University of Medicine, Shiyan.
Department of Pharmaceutics, Shanghai Eighth People's Hospital, Jiangsu University, Shanghai, People's Republic of China.
Int J Nanomedicine. 2016 Oct 3;11:4991-5002. doi: 10.2147/IJN.S114302. eCollection 2016.
As one of the natural herbal flavonoids, myricetin has attracted much research interest, mainly owing to its remarkable anticancer properties and negligible side effects. It holds great potential to be developed as an ideal anticancer drug through improving its bioavailability. This study was performed to investigate the effects of Pluronic-based micelle encapsulation on myricetin-induced cytotoxicity and the mechanisms underlying its anticancer properties in human glioblastoma cells. Cell viability was assessed using a methylthiazol tetrazolium assay and a real-time cell analyzer. Immunoblotting and quantitative reverse transcriptase polymerase chain reaction techniques were used for determining the expression levels of related molecules in protein and mRNA. The results indicated that myricetin-induced cytotoxicity was highly potentiated by the encapsulation of myricetin. Mitochondrial apoptotic pathway was demonstrated to be involved in myricetin-induced glioblastoma cell death. The epidermal growth factor receptor (EGFR)/PI3K/Akt pathway located in the plasma membrane and cytosol and the RAS-ERK pathway located in mitochondria served as upstream and downstream targets, respectively, in myricetin-induced apoptosis. MiR-21 inhibitors interrupted the expression of EGFR, p-Akt, and K-Ras in the same fashion as myricetin-loaded mixed micelles (MYR-MCs) and miR-21 expression were dose-dependently inhibited by MYR-MCs, indicating the interaction of miR-21 with MYR-MCs. This study provided evidence supportive of further development of MYR-MC formulation for preferentially targeting mitochondria of glioblastoma cells.
作为天然植物类黄酮之一,杨梅素因其显著的抗癌特性和可忽略不计的副作用而备受研究关注。通过提高其生物利用度,杨梅素具有被开发成为理想抗癌药物的巨大潜力。本研究旨在探讨基于普朗尼克的胶束包封对杨梅素诱导的细胞毒性的影响及其在人胶质母细胞瘤细胞中的抗癌作用机制。使用甲基噻唑四氮唑法和实时细胞分析仪评估细胞活力。采用免疫印迹和定量逆转录聚合酶链反应技术测定相关分子在蛋白质和mRNA水平的表达。结果表明,杨梅素的包封显著增强了其诱导的细胞毒性。线粒体凋亡途径参与了杨梅素诱导的胶质母细胞瘤细胞死亡。位于质膜和胞质溶胶中的表皮生长因子受体(EGFR)/PI3K/Akt途径以及位于线粒体中的RAS-ERK途径分别作为杨梅素诱导凋亡的上游和下游靶点。miR-21抑制剂与载杨梅素混合胶束(MYR-MCs)以相同方式阻断EGFR、p-Akt和K-Ras的表达,且MYR-MCs剂量依赖性抑制miR-21表达,表明miR-21与MYR-MCs之间存在相互作用。本研究为进一步开发优先靶向胶质母细胞瘤细胞线粒体的MYR-MC制剂提供了支持证据。