中华超声影像学杂志
中華超聲影像學雜誌
중화초성영상학잡지
CHINESE JOURNAL OF ULTRASONOGRAPHY
2012年
7期
621-624
,共4页
胡劼%宗瑜瑾%宋宏萍%张景瑶%段艳%张军%周晓东%苏海砾
鬍劼%宗瑜瑾%宋宏萍%張景瑤%段豔%張軍%週曉東%囌海礫
호할%종유근%송굉평%장경요%단염%장군%주효동%소해력
超声检查%微气泡%肾肿瘤%细胞凋亡%舒尼替尼
超聲檢查%微氣泡%腎腫瘤%細胞凋亡%舒尼替尼
초성검사%미기포%신종류%세포조망%서니체니
Ultrasonography%Microbubbles%Kidney neoplasms%Apoptosis%Sunitinib
目的 观察新型多聚体微泡携带舒尼替尼对人肾癌GRC-1细胞生长及凋亡的影响.方法 将体外培养的人肾癌GRC-1细胞随机分为6组:空白对照组、单纯微泡组、单纯脂质体组、舒尼替尼组、新型多聚体微泡载舒尼替尼不联合超声组、新型多聚体微泡载舒尼替尼联合超声组.MTT法观察不同处理组细胞生存率,Sigma-FITC荧光染色及透射电镜检测细胞凋亡.结果 新型多聚体微泡载舒尼替尼联合超声组对人肾癌GRC-1细胞的生长抑制及促进凋亡作用强于其他处理组及对照组.结论 新型多聚体微泡携带舒尼替尼在超声作用下对人肾癌GRC-1细胞生长有明显抑制作用,并诱导细胞凋亡.
目的 觀察新型多聚體微泡攜帶舒尼替尼對人腎癌GRC-1細胞生長及凋亡的影響.方法 將體外培養的人腎癌GRC-1細胞隨機分為6組:空白對照組、單純微泡組、單純脂質體組、舒尼替尼組、新型多聚體微泡載舒尼替尼不聯閤超聲組、新型多聚體微泡載舒尼替尼聯閤超聲組.MTT法觀察不同處理組細胞生存率,Sigma-FITC熒光染色及透射電鏡檢測細胞凋亡.結果 新型多聚體微泡載舒尼替尼聯閤超聲組對人腎癌GRC-1細胞的生長抑製及促進凋亡作用彊于其他處理組及對照組.結論 新型多聚體微泡攜帶舒尼替尼在超聲作用下對人腎癌GRC-1細胞生長有明顯抑製作用,併誘導細胞凋亡.
목적 관찰신형다취체미포휴대서니체니대인신암GRC-1세포생장급조망적영향.방법 장체외배양적인신암GRC-1세포수궤분위6조:공백대조조、단순미포조、단순지질체조、서니체니조、신형다취체미포재서니체니불연합초성조、신형다취체미포재서니체니연합초성조.MTT법관찰불동처리조세포생존솔,Sigma-FITC형광염색급투사전경검측세포조망.결과 신형다취체미포재서니체니연합초성조대인신암GRC-1세포적생장억제급촉진조망작용강우기타처리조급대조조.결론 신형다취체미포휴대서니체니재초성작용하대인신암GRC-1세포생장유명현억제작용,병유도세포조망.
Objective To investigate the effect of growth inhibition and apoptosis induction of sunitinib-liposome-loaded microbubbles on renal carcinoma cell strain.Methods GRC-1 cell strain was cultured in vitro,and was divided into 6 groups:blank control group,pure microbubbles group,pure lipsomes group,sunitinib group,sunitinib-liposome-loaded microbubbles without ultrasound treat group,sunitinib liposome-loaded microbubbles with ultrasound treat group.Growth inhibition in different groups was observed at different time with MTT assay,apoptosis induction with Sigma-FlTC technology and transmission electron microscope.Results The growth inhibition and apoptosis promotion of GRC-1 cell were significantly increased in sunitinib-liposome-loaded microbubbles with ultrasound treat group compared to the other groups.Conclusions Microbubble guided sunitinih delivery can increase the effect of the growth inhibition and apoptosis induction of GRC-1 cells,which may provide an more effective approach for cancer treatment.