国际遗传学杂志
國際遺傳學雜誌
국제유전학잡지
INTERNATIONAL JOURNAL OF GENETICS
2011年
3期
135-140,152
,共7页
张杰武%李燕华%聂春磊%孔令宇%徐晋
張傑武%李燕華%聶春磊%孔令宇%徐晉
장걸무%리연화%섭춘뢰%공령우%서진
△Np63%RNA干扰%头颈鳞癌%细胞增殖
△Np63%RNA榦擾%頭頸鱗癌%細胞增殖
△Np63%RNA간우%두경린암%세포증식
△Np63%RNAi%Head and neck squamous cell carcinomas%Cell proliferation
目的 研究 △△Np63促进头颈鳞癌细胞增殖及存活的作用及相关分子机制.方法 筛选高表达△Np63 的头颈鳞癌细胞系,采用RNAi方法分别抑制△Np63及P63表达.RT-PCR、Western印迹、MTT法、流式细胞术等检测细胞增殖和细胞周期等生物学行为改变;并检测相关周期调控蛋白的表达.结果 △Np63在FaDu细胞中高表达,定位于细胞核.抑制△Np63及P63表达后,FaDu细胞增殖能力明显下降(t=3.66,P<0.01),发生G1期细胞周期阻滞;CDK抑制物P21及P27蛋白表达上调,P53表达上调.结论 △Np63对FaDu细胞增殖及存活发挥主导作用,△Np63通过抑制p21、p27的表达,促进肿瘤细胞的生长和增殖.
目的 研究 △△Np63促進頭頸鱗癌細胞增殖及存活的作用及相關分子機製.方法 篩選高錶達△Np63 的頭頸鱗癌細胞繫,採用RNAi方法分彆抑製△Np63及P63錶達.RT-PCR、Western印跡、MTT法、流式細胞術等檢測細胞增殖和細胞週期等生物學行為改變;併檢測相關週期調控蛋白的錶達.結果 △Np63在FaDu細胞中高錶達,定位于細胞覈.抑製△Np63及P63錶達後,FaDu細胞增殖能力明顯下降(t=3.66,P<0.01),髮生G1期細胞週期阻滯;CDK抑製物P21及P27蛋白錶達上調,P53錶達上調.結論 △Np63對FaDu細胞增殖及存活髮揮主導作用,△Np63通過抑製p21、p27的錶達,促進腫瘤細胞的生長和增殖.
목적 연구 △△Np63촉진두경린암세포증식급존활적작용급상관분자궤제.방법 사선고표체△Np63 적두경린암세포계,채용RNAi방법분별억제△Np63급P63표체.RT-PCR、Western인적、MTT법、류식세포술등검측세포증식화세포주기등생물학행위개변;병검측상관주기조공단백적표체.결과 △Np63재FaDu세포중고표체,정위우세포핵.억제△Np63급P63표체후,FaDu세포증식능력명현하강(t=3.66,P<0.01),발생G1기세포주기조체;CDK억제물P21급P27단백표체상조,P53표체상조.결론 △Np63대FaDu세포증식급존활발휘주도작용,△Np63통과억제p21、p27적표체,촉진종류세포적생장화증식.
Objective To investigate the functional role of △Np63, the main isoform of P63, in promoting cell proliferation and survival in head and neck squamous cell carcinoma (HNSCC). Methods △Np63 overexpressing cell line was selected from several HNSCC cell lines. Specific △Np63 siRNAs and p63 siRNAs were individually transfected into FaDu cells for 48h and 72h which overexpressing △Np63. The expression levels of △Np63 mRNA and protein were analyzed by RT-PCR,Western blot and immunohistochemistry respectively.The cell proliferation was determined by MTT assay.The distribution of cell cycle was assessed by flow cytometry.The protein expression level of P21, P27 and P53 were detected by Western blot. Results △Np63 is highly expressed in FaDu cell line, especially located in the nucleus.The growth rate of FaDu cells transfected with △Np63-siRNA and p63-siRNA was significantly decreased(t=3.66,P<0.01),and cell cycle mainly arrested in G1 phase. Further studies show that the down-requlation of △Np63 results in the overexpression of P53 and upregulation of CKIs , including P21 and P27 at protein levels. Conclusion △Np63 inhibit the expression of p21 and p27 to promote the proliferation of HNSCC cells , playing a role in maintenance of cell proliferation and survival.