中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2011年
5期
787-788
,共2页
王玉峰%李良满%胡春吉%柴利鹏
王玉峰%李良滿%鬍春吉%柴利鵬
왕옥봉%리량만%호춘길%시리붕
骨肉瘤%甲氨蝶呤%二硫代氨基甲酸吡咯烷%Livin
骨肉瘤%甲氨蝶呤%二硫代氨基甲痠吡咯烷%Livin
골육류%갑안접령%이류대안기갑산필각완%Livin
Osteosarcoma%Methotrexate%Pyrrolidine dithiocarbamate%Livin
目的 观察二硫代氨基甲酸吡咯烷(PDTC)和甲氨蝶呤(MTX)对人骨肉瘤MG-63细胞凋亡和Livin表达的影响.方法 体外培养骨肉瘤MG-63细胞株,用0、50、100、200和400μmol/L的PDTC和MTX作用于骨肉瘤MG-63细胞24、48和72 h后,用噻唑蓝(MTT)比色法检测骨肉瘤MG-63细胞的增殖活性,用流式细胞仪测细胞的凋亡率,用Western blot检测各组细胞的Livin蛋白表达水平.结果 各组骨肉瘤MG-63细胞的增殖活性随着时间增加降低,同时细胞的凋亡率随着时间增加(P<0.05),各组细胞中Livin蛋白的表达明显降低(P<0.05).结论 PDTC能提高MTX对骨肉瘤MG-63细胞的凋亡,其机制可能与下调Livin表达,阻断了Livin介导的抗凋亡途径有关.
目的 觀察二硫代氨基甲痠吡咯烷(PDTC)和甲氨蝶呤(MTX)對人骨肉瘤MG-63細胞凋亡和Livin錶達的影響.方法 體外培養骨肉瘤MG-63細胞株,用0、50、100、200和400μmol/L的PDTC和MTX作用于骨肉瘤MG-63細胞24、48和72 h後,用噻唑藍(MTT)比色法檢測骨肉瘤MG-63細胞的增殖活性,用流式細胞儀測細胞的凋亡率,用Western blot檢測各組細胞的Livin蛋白錶達水平.結果 各組骨肉瘤MG-63細胞的增殖活性隨著時間增加降低,同時細胞的凋亡率隨著時間增加(P<0.05),各組細胞中Livin蛋白的錶達明顯降低(P<0.05).結論 PDTC能提高MTX對骨肉瘤MG-63細胞的凋亡,其機製可能與下調Livin錶達,阻斷瞭Livin介導的抗凋亡途徑有關.
목적 관찰이류대안기갑산필각완(PDTC)화갑안접령(MTX)대인골육류MG-63세포조망화Livin표체적영향.방법 체외배양골육류MG-63세포주,용0、50、100、200화400μmol/L적PDTC화MTX작용우골육류MG-63세포24、48화72 h후,용새서람(MTT)비색법검측골육류MG-63세포적증식활성,용류식세포의측세포적조망솔,용Western blot검측각조세포적Livin단백표체수평.결과 각조골육류MG-63세포적증식활성수착시간증가강저,동시세포적조망솔수착시간증가(P<0.05),각조세포중Livin단백적표체명현강저(P<0.05).결론 PDTC능제고MTX대골육류MG-63세포적조망,기궤제가능여하조Livin표체,조단료Livin개도적항조망도경유관.
Objective To detect the effect of pyirolidine dithiocarbamate (PDTC) and methotrexate (MTX) on apoptosis and expression of livin of human osteosarcoma MG-63 cells. Methods MG-63 cells were cultured in vitro. At 24, 48 and 72 h after treatment of PDTC and MTX at different concentrations (0, 50, 100, 200 and 400 μmol/L) , MTT assay was used to observe the growth inhibition of MG-63 cells. The apoptosis was assessed by flow cytometry. The protein expression of livin was detected by Westem blotting. Results When PDTC and MTX were added, growth inhibition and increased apoptosis of MG-63 cells were detected. The protein expression level of livin was down-regulated obviously ( P <0. 05). Conclusion PDTC can promote the apoptosis of MTX-treated MG-63 cells, which may be correlated with down-regulation of the livin expression.