中国病理生理杂志
中國病理生理雜誌
중국병리생리잡지
CHINESE JOURNAL OF PATHOPHYSIOLOGY
2014年
8期
1379-1383
,共5页
金海东%戴兵%蔡建武%陈辉%范时洋%潘骏
金海東%戴兵%蔡建武%陳輝%範時洋%潘駿
금해동%대병%채건무%진휘%범시양%반준
软骨肉瘤%白藜芦醇%PI3K/Akt通路%细胞凋亡
軟骨肉瘤%白藜蘆醇%PI3K/Akt通路%細胞凋亡
연골육류%백려호순%PI3K/Akt통로%세포조망
Chondrosarcoma%Resveratrol%PI3K/Aktpathway%Apoptosis
目的:探讨白藜芦醇抑制软骨肉瘤的机制及对线粒体途径和PI3K/Akt通路的影响。方法:SW1353软骨肉瘤细胞培养至对数生长期后设对照组和白藜芦醇处理组,药物处理组用25、50和100μmol/L白藜芦醇处理24 h、48 h或72 h。采用CCK8法检测SW1353软骨肉瘤细胞的活力,Hoechst 33258荧光染色观察细胞凋亡,Western blotting检测activated caspase-3、Bcl-2、Bax、Akt和p-Akt蛋白在细胞中表达情况,细胞划痕实验观察细胞迁移情况。结果:白藜芦醇处理后细胞活力下降,呈时间-剂量依赖性(P<0.01)。 Hoechst 33258染色检测可见药物处理组有明显的细胞凋亡核象。 Western blotting 检测显示药物处理组activated caspase-3和Bax蛋白表达上调,Bcl-2蛋白和p-Akt蛋白表达下调,总Akt改变不显著。细胞划痕试验显示,白藜芦醇能显著抑制SW1353细胞的迁移。结论:白藜芦醇能够诱导软骨肉瘤凋亡,部分是通过线粒体途径及PI3K/Akt信号通路发挥作用。
目的:探討白藜蘆醇抑製軟骨肉瘤的機製及對線粒體途徑和PI3K/Akt通路的影響。方法:SW1353軟骨肉瘤細胞培養至對數生長期後設對照組和白藜蘆醇處理組,藥物處理組用25、50和100μmol/L白藜蘆醇處理24 h、48 h或72 h。採用CCK8法檢測SW1353軟骨肉瘤細胞的活力,Hoechst 33258熒光染色觀察細胞凋亡,Western blotting檢測activated caspase-3、Bcl-2、Bax、Akt和p-Akt蛋白在細胞中錶達情況,細胞劃痕實驗觀察細胞遷移情況。結果:白藜蘆醇處理後細胞活力下降,呈時間-劑量依賴性(P<0.01)。 Hoechst 33258染色檢測可見藥物處理組有明顯的細胞凋亡覈象。 Western blotting 檢測顯示藥物處理組activated caspase-3和Bax蛋白錶達上調,Bcl-2蛋白和p-Akt蛋白錶達下調,總Akt改變不顯著。細胞劃痕試驗顯示,白藜蘆醇能顯著抑製SW1353細胞的遷移。結論:白藜蘆醇能夠誘導軟骨肉瘤凋亡,部分是通過線粒體途徑及PI3K/Akt信號通路髮揮作用。
목적:탐토백려호순억제연골육류적궤제급대선립체도경화PI3K/Akt통로적영향。방법:SW1353연골육류세포배양지대수생장기후설대조조화백려호순처리조,약물처리조용25、50화100μmol/L백려호순처리24 h、48 h혹72 h。채용CCK8법검측SW1353연골육류세포적활력,Hoechst 33258형광염색관찰세포조망,Western blotting검측activated caspase-3、Bcl-2、Bax、Akt화p-Akt단백재세포중표체정황,세포화흔실험관찰세포천이정황。결과:백려호순처리후세포활력하강,정시간-제량의뢰성(P<0.01)。 Hoechst 33258염색검측가견약물처리조유명현적세포조망핵상。 Western blotting 검측현시약물처리조activated caspase-3화Bax단백표체상조,Bcl-2단백화p-Akt단백표체하조,총Akt개변불현저。세포화흔시험현시,백려호순능현저억제SW1353세포적천이。결론:백려호순능구유도연골육류조망,부분시통과선립체도경급PI3K/Akt신호통로발휘작용。
[ABSTRACT]AIM:Toinvestigatetheinhibitoryeffectsofresveratrolonchondrosarcomaandtherelationwith mitochondrial and PI3K/Akt pathways.METHODS:Chondrosarcoma SW1353 cells were treated with resveratrol at con-centrations of 25, 50 and 100 μmol/L for the time intervals of 24 h, 48 h and 72 h.The viability and apoptosis of the SW1353 cells in the presence or absence of resveratrol were analyzed by CCK 8 assay and Hoechst 33258 staining , respec-tively.The protein levels of Bcl-2, Bax, activated caspase-3, Akt and p-Akt were detected by Western blotting .The cell migration ability was determined by wound scratch assay .RESULTS:Exposure of the cells to resveratrol resulted in a de-crease in the cell viability in a dose-and time-dependent manner (P<0.05).visible nuclei with apoptotic characteristics in resveratrol group were observed .The protein levels of activated caspase-3 and Bax were increased , and Bcl-2 and p-Akt were decreased compared with control group .The total Akt were not significantly changed .Resveratrol also significantly re-duced the migration of tumor cells .CONCLUSION:Resveratrol induces apoptosis of chondrosarcoma , which plays a role of part through mitochondrial and PI 3K/Akt signaling pathways .