中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2013年
9期
1807-1809
,共3页
范月超%陈洪福%郑骏年%张慧%梅鹏金%纪建永%颜丙超%雷霆
範月超%陳洪福%鄭駿年%張慧%梅鵬金%紀建永%顏丙超%雷霆
범월초%진홍복%정준년%장혜%매붕금%기건영%안병초%뢰정
胶质瘤%增殖%细胞周期
膠質瘤%增殖%細胞週期
효질류%증식%세포주기
Glioma%Proliferation%Cell cycle
目的 观察热休克蛋白70羧基末端相互作用蛋白(CHIP)小干扰RNA(siRNA)对人脑胶质瘤细胞周期及增殖的影响.方法 运用Control siRNA、CHIP siRNA分别转染原代培养人脑胶质瘤细胞,Western blot检测CHIP蛋白表达,流式细胞仪检测CHIP siRNA对原代培养人脑胶质瘤细胞周期的影响,细胞计数试剂盒(CCK-8)细胞增殖实验检测CHIP siRNA对原代培养人脑胶质瘤细胞增殖的影响.结果 与Control siRNA组比较CHIP siRNA组原代培养人脑胶质瘤细胞CHIP蛋白表达量降低53.3%,CHIP siRNA组原代培养人脑胶质瘤细胞增殖细胞数增加,并且G1期细胞数所占比例减少14.1%,S期细胞数所占比例增加13.7% (P <0.05).结论 CHIP siRNA靶向干扰了CHIP的表达,CHIP作为肿瘤抑癌因子抑制脑胶质瘤细胞的增殖,并能使细胞阻滞在G1期.
目的 觀察熱休剋蛋白70羧基末耑相互作用蛋白(CHIP)小榦擾RNA(siRNA)對人腦膠質瘤細胞週期及增殖的影響.方法 運用Control siRNA、CHIP siRNA分彆轉染原代培養人腦膠質瘤細胞,Western blot檢測CHIP蛋白錶達,流式細胞儀檢測CHIP siRNA對原代培養人腦膠質瘤細胞週期的影響,細胞計數試劑盒(CCK-8)細胞增殖實驗檢測CHIP siRNA對原代培養人腦膠質瘤細胞增殖的影響.結果 與Control siRNA組比較CHIP siRNA組原代培養人腦膠質瘤細胞CHIP蛋白錶達量降低53.3%,CHIP siRNA組原代培養人腦膠質瘤細胞增殖細胞數增加,併且G1期細胞數所佔比例減少14.1%,S期細胞數所佔比例增加13.7% (P <0.05).結論 CHIP siRNA靶嚮榦擾瞭CHIP的錶達,CHIP作為腫瘤抑癌因子抑製腦膠質瘤細胞的增殖,併能使細胞阻滯在G1期.
목적 관찰열휴극단백70최기말단상호작용단백(CHIP)소간우RNA(siRNA)대인뇌효질류세포주기급증식적영향.방법 운용Control siRNA、CHIP siRNA분별전염원대배양인뇌효질류세포,Western blot검측CHIP단백표체,류식세포의검측CHIP siRNA대원대배양인뇌효질류세포주기적영향,세포계수시제합(CCK-8)세포증식실험검측CHIP siRNA대원대배양인뇌효질류세포증식적영향.결과 여Control siRNA조비교CHIP siRNA조원대배양인뇌효질류세포CHIP단백표체량강저53.3%,CHIP siRNA조원대배양인뇌효질류세포증식세포수증가,병차G1기세포수소점비례감소14.1%,S기세포수소점비례증가13.7% (P <0.05).결론 CHIP siRNA파향간우료CHIP적표체,CHIP작위종류억암인자억제뇌효질류세포적증식,병능사세포조체재G1기.
Objective To investigate the effect of carboxyl terminus of Hsc70-interacting protein (CHIP) small interfering RNA (siRNA) on cell cycle and proliferation of human brain glioma cells.Methods Control siRNA and CHIP siRNA were used respectively to transfect primary cultured human brain glioma cells.The expression levels of CHIP in primary cultured human brain glioma cells were detected after CHIP knockdown by using Western blotting.The influence of CHIP knockdown on the cell cycle of primary cultured human brain glioma cells was measured by flow cytometry.The influence of CHIP knockdown on the proliferation of primary cultured human brain glioma cells was tested by using cell counting kit-8 (CCK-8)assay.Results As compared with control siRNA group,the expression of CHIP was decreased by 53.3% in CHIP siRNA group.CHIP knockdown could drastically increase the ability of proliferation in primary cultured human brain glioma cells,increase the S phase ratio of cell cycle by 13.7% and decrease the G1 phase ratio of cell cycle by 14.1% (both P < 0.05).Conclusion CHIP-targeted siRNA interferes with the expression levels of CHIP.CHIP acts as a tumor suppressor that suppresses the proliferation of glioma cells and arrests the cells in G1 phase.