紫杉醇载药胶束对人肺癌A549细胞增殖与凋亡的影响
Effects of paclitaxel loaded-drug micelles on cell proliferation and apoptosis of human lung cancer A549 cells
-
摘要: 本文研究了以聚乙二醇-聚己内酯共聚物为载体制备的紫杉醇载药胶束 (mPEG-PCL-PTX) 对人肺癌A549细胞增殖和凋亡的影响, 探讨其抗肿瘤的可能机制。以体外培养的人肺癌A549细胞为研究对象, 四甲基偶氮唑盐 (MTT) 法检测mPEG-PCL-PTX对细胞增殖的抑制作用; 流式细胞仪检测细胞周期; Hoechst/PI染色检测细胞凋亡; RT-PCR检测A549细胞Bax、Bcl-2、Caspase-3 mRNA的表达; Western blot检测A549细胞Bax、Bcl-2蛋白表达。结果显示, 空白聚合物胶束体外基本无毒性, mPEG-PCL-PTX对A549细胞增殖有明显抑制作用, 并使细胞周期阻滞于G2/M期; 载药胶束促进A549细胞凋亡, 使A549细胞Bcl-2基因和蛋白表达下调, Bax表达上调, 同时上调Caspase-3基因表达。结果表明, 含腙键pH敏感聚合物体外基本无毒性, 载药胶束mPEG-PCL- PTX对人肺癌A549细胞的增殖有抑制作用, 对A549细胞的凋亡有促进作用。Abstract: This study was conducted to investigate the paclitaxel loaded by hydrazone bonds in poly(ethylene glycol)-poly(caprolactone) micelles (mPEG-PCL-PTX) on proliferation and apoptosis of human lung cancer A549 cells and its possible mechanisms of anti-tumor activity. The cell proliferation was measured with MTT assay. Flow cytometry were used to analyze the cell cycle. The cell apoptosis was analyzed using Hoechst/PI staining. The expression levels of apoptotic genes expression in the mitochondrial apoptosis pathway were detected by RT-PCR and Western blotting, respectively. The mPEG-PCL-PTX could inhibit the proliferation of A549 cells and promote the apoptosis. The Bax, caspase-3 protein expression were increased while Bcl-2 protein expression was decreased in A549 cells. Results showed that the polymer containing hydrazone bond is non-toxic in vitro, the mPEG-PCL-PTX micelles can inhibit the proliferation and induce the apoptosis of A549 cells.
下载: