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出 处:《中华实验外科杂志》2012年第1期95-96,共2页Chinese Journal of Experimental Surgery
摘 要:目的以体外培养的U251细胞为模型,观察曲古抑菌素A(TSA)联合单纯疱疹病毒I型(HSV-1)对肿瘤细胞增殖、凋亡的影响。方法以0.5×10^-3mol/LTSA和10MOIHSV-1及0.5×10^-3μmol/LTSA与10MOIHSV-1组合作用于U251人胶质瘤细胞,72h后噻唑蓝(MTr)比色法检测各组细胞增殖情况,显微镜下观察各组细胞形态,流式细胞仪检测各组细胞的凋亡情况。结果单一TSA组、单一HSV-1组、TSA与HSV一1联合组U251细胞增殖抑制率分别为(48.0±1.8)%、(18.0±3.1)%、(58.0±5.8)%;凋亡率分别为(47.4±3.5)%、(29.6±3.0)%、(59.6±4.0)%。TSA与HSV-1联合组U251细胞增殖抑制率及凋亡率明显高于单一使用TSA或HSV-1组(P〈0.01)。结论TSA联合HSV-1对体外培养的U251细胞具有协同或叠加杀伤作用。Objective To observe the effects of trichostain A (TSA) combined with herpes sim- plex virus-1 (HSV-1) on proliferation and apoptosis in U251 cells in vitro. Methods U251 ceils in vitro were treated separately with 0.5×10^-3μmol/Lmol/L TSA (TSA group), 10 MOI HSV-1 (HSV-1 group), and 0.5×10^-3μmol/L TSA combined with 10 MOI HSV-1 (TSA + HSV-1 group) for 72 h. The methyl thia- zol tetrazolium (MTT) assay was used to observe the proliferation of U251 cells. The cellular morphological changes were observed under a ruicroscope. The apoptosis rate was analyzed by using flow cytometry. Resuits In TSA group, HSV-1 group, TSA + HSV-1 group, the proliferation inhibition rate of the U251 cells was (48.0±1.8)%, (18.0±3.1)%, and (58.0±5.8)%; Apoptosis rate was (47.4±3.5)%, (29.6±3.0) %, and ( 59. 6±4. 0 ) % respectively. The inhibitory effects of proliferation or apoptosis in TSA± HSV-1 group was stronger than TSA group or HSV-1 group ( P 〈 0. 01 ). Conclusion TSA combined with HSV-1 has a synergistic killing effect on cultured U251 cells.
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