现代肿瘤医学
現代腫瘤醫學
현대종류의학
JOURNAL OF MODERN ONCOLOGY
2014年
8期
1744-1747
,共4页
公方和%叶景%刘一兵%白红民%刘帅%王伟民%王国良
公方和%葉景%劉一兵%白紅民%劉帥%王偉民%王國良
공방화%협경%류일병%백홍민%류수%왕위민%왕국량
14 - 3 - 3β%胶质瘤细胞%β - catenin
14 - 3 - 3β%膠質瘤細胞%β - catenin
14 - 3 - 3β%효질류세포%β - catenin
14 - 3 - 3β%glioma cell%β - catenin
目的:研究14-3-3β基因在胶质瘤细胞生长和增殖中的调控作用。方法:构建14-3-3β基因过表达质粒并设计14-3-3β基因和β- catenin 基因 siRNAs,分组转染人体正常神经星形胶质细胞系 SVGp12和胶质瘤细胞系 U87,噻唑蓝(MTT)法观察14-3-3β基因过表达/沉默和β- catenin 基因沉默对细胞生长和增殖的影响,并利用 qRT - PCR 定量分析受调控原癌基因的表达变化。结果:14-3-3β基因过表达的星形胶质细胞生长能力显著高于对照组(P ﹤0.05),而β- catenin 基因沉默的星形胶质细胞生长受到明显抑制(P ﹤0.05)。观察到14-3-3β基因或β- catenin 基因沉默的胶质瘤细胞生长能力也显著低于对照组细胞(P ﹤0.05)。结论:胶质瘤细胞的生长和增殖受到14-3-3β基因的调控并且其调控是通过β- catenin 基因来进行的,但其具体的信号调控机制需要进一步探讨。
目的:研究14-3-3β基因在膠質瘤細胞生長和增殖中的調控作用。方法:構建14-3-3β基因過錶達質粒併設計14-3-3β基因和β- catenin 基因 siRNAs,分組轉染人體正常神經星形膠質細胞繫 SVGp12和膠質瘤細胞繫 U87,噻唑藍(MTT)法觀察14-3-3β基因過錶達/沉默和β- catenin 基因沉默對細胞生長和增殖的影響,併利用 qRT - PCR 定量分析受調控原癌基因的錶達變化。結果:14-3-3β基因過錶達的星形膠質細胞生長能力顯著高于對照組(P ﹤0.05),而β- catenin 基因沉默的星形膠質細胞生長受到明顯抑製(P ﹤0.05)。觀察到14-3-3β基因或β- catenin 基因沉默的膠質瘤細胞生長能力也顯著低于對照組細胞(P ﹤0.05)。結論:膠質瘤細胞的生長和增殖受到14-3-3β基因的調控併且其調控是通過β- catenin 基因來進行的,但其具體的信號調控機製需要進一步探討。
목적:연구14-3-3β기인재효질류세포생장화증식중적조공작용。방법:구건14-3-3β기인과표체질립병설계14-3-3β기인화β- catenin 기인 siRNAs,분조전염인체정상신경성형효질세포계 SVGp12화효질류세포계 U87,새서람(MTT)법관찰14-3-3β기인과표체/침묵화β- catenin 기인침묵대세포생장화증식적영향,병이용 qRT - PCR 정량분석수조공원암기인적표체변화。결과:14-3-3β기인과표체적성형효질세포생장능력현저고우대조조(P ﹤0.05),이β- catenin 기인침묵적성형효질세포생장수도명현억제(P ﹤0.05)。관찰도14-3-3β기인혹β- catenin 기인침묵적효질류세포생장능력야현저저우대조조세포(P ﹤0.05)。결론:효질류세포적생장화증식수도14-3-3β기인적조공병차기조공시통과β- catenin 기인래진행적,단기구체적신호조공궤제수요진일보탐토。
To study the role of 14 - 3 - 3β on the regulation of the growth and proliferation of glioma cell. Methods:Recombinant plasmids containing 14 - 3 - 3β and small - interfering RNAs(siRNAs)targeting 14 - 3- 3β or β - catenin were transfected into the human normal astrocyte line SVGp12 and glioma cell line U87,respec-tively. The growth and proliferation of the transfected cells was analyzed by MTT assay. The expression of the oncogene was also analyzed by qRT - PCR. Results:Compared to the control,14 - 3 - 3β overexpression significantly promoted the growth of astrocyte cells(P ﹤ 0. 05). Meanwhile knockdown of β - catenin by siRNA blocked cell proliferation in-duced by overexpression of 14 - 3 - 3β(P ﹤ 0. 05). It was also observed that the proliferation of glioma cell was in-hibited by knockdown of either 14 - 3 - 3β or β - catenin by siRNA(P ﹤ 0. 05). Conclusion:The growth and prolif-eration of glioma cell was regulated by 14 - 3 - 3β,which was mediated by β - catenin. However,the precise underly-ing molecular mechanism needs to be further elucidated.