中华肿瘤杂志
中華腫瘤雜誌
중화종류잡지
CHINESE JOURNAL OF ONCOLOGY
2013年
8期
572-578
,共7页
公小迪%袁海花%王炯轶%郭跃辉%时婧%姜斌
公小迪%袁海花%王炯軼%郭躍輝%時婧%薑斌
공소적%원해화%왕형질%곽약휘%시청%강빈
肺肿瘤%表皮生长因子受体酪氨酸激酶抑制剂%AG1478%叉头转录因子M1%叉头转录因子O3a%细胞增殖%药物敏感性
肺腫瘤%錶皮生長因子受體酪氨痠激酶抑製劑%AG1478%扠頭轉錄因子M1%扠頭轉錄因子O3a%細胞增殖%藥物敏感性
폐종류%표피생장인자수체락안산격매억제제%AG1478%차두전록인자M1%차두전록인자O3a%세포증식%약물민감성
Lung neoplasms%Epidermal growth factor receptor-tyrosine kinase inhibitor%AG1478%Forkhead transcription factor M1%Forkhead transcription factors O3a%Cell proliferation%Drug sensitivity
目的 探讨表皮生长因子受体酪氨酸激酶抑制剂AG1478对非小细胞肺癌细胞中叉头转录因子M1 (FOXM1)、叉头转录因子O3a(FOXO3a)的表达调控,以及RNA干扰技术下调FOXM1、FOXO3a的表达后对肺癌细胞增殖及其对AG1478药物敏感性的影响.方法 采用逆转录聚合酶链反应(RT-PCR)和Western blot法检测肺腺癌细胞株A549中FOXM1和FOXO3a mRNA和蛋白的表达情况;瞬时转染FOXM1和FOXO3a小干扰RNA (siRNA)后,RT-PCR和Western blot法检测转染效率和相关蛋白的表达;采用CCK-8法、集落形成实验和流式细胞仪分别检测细胞增殖、集落形成能力及细胞周期分布的改变.结果 AG1478呈时间依赖性抑制FOXM1 mRNA和蛋白的表达(均P<0.05).转染FOXM1 siRNA后,FOXM1 mRNA和蛋白及其细胞周期蛋白B1(cyclin B1)、c-Myc、Bcl-2蛋白的表达明显下降,p21和剪切后多腺苷二磷酸核糖聚合酶(cleaved-PARP)蛋白的表达则明显上调(均P <0.05).空白组、阴性对照组和FOXM1 siRNA转染组的集落数分别为(135.3±7.0)个、(125.3±7.5)个和(37.3±8.6)个,阴性对照组和FOXM1 siRNA转染组的集落形成抑制率分别为(7.40±0.94)%和(72.40±6.09)%(P<0.05).FOXM1 siRNA转染组的G2/M期细胞比例为(55.60±4.83)%,明显高于空白组[(24.30±1.95)%]和阴性对照组[(21.30±2.06)%,P<0.05].转染FOXM1 siRNA后,可明显增加A549细胞对AG1478的药物敏感性(P<0.05).AG1478可诱导活化的FOXO3a分子表达并促进其核定位;转染FOXO3a siRNA后,FOXM1蛋白水平明显上调,并通过活化的AKT削弱AG1478对FOXM1表达的抑制.结论 AG1478通过诱导活化的FOXO3a表达及胞核重定位,下调FOXM1的表达,进而抑制肺癌细胞增殖,增加肺癌细胞对AG1478的敏感性.
目的 探討錶皮生長因子受體酪氨痠激酶抑製劑AG1478對非小細胞肺癌細胞中扠頭轉錄因子M1 (FOXM1)、扠頭轉錄因子O3a(FOXO3a)的錶達調控,以及RNA榦擾技術下調FOXM1、FOXO3a的錶達後對肺癌細胞增殖及其對AG1478藥物敏感性的影響.方法 採用逆轉錄聚閤酶鏈反應(RT-PCR)和Western blot法檢測肺腺癌細胞株A549中FOXM1和FOXO3a mRNA和蛋白的錶達情況;瞬時轉染FOXM1和FOXO3a小榦擾RNA (siRNA)後,RT-PCR和Western blot法檢測轉染效率和相關蛋白的錶達;採用CCK-8法、集落形成實驗和流式細胞儀分彆檢測細胞增殖、集落形成能力及細胞週期分佈的改變.結果 AG1478呈時間依賴性抑製FOXM1 mRNA和蛋白的錶達(均P<0.05).轉染FOXM1 siRNA後,FOXM1 mRNA和蛋白及其細胞週期蛋白B1(cyclin B1)、c-Myc、Bcl-2蛋白的錶達明顯下降,p21和剪切後多腺苷二燐痠覈糖聚閤酶(cleaved-PARP)蛋白的錶達則明顯上調(均P <0.05).空白組、陰性對照組和FOXM1 siRNA轉染組的集落數分彆為(135.3±7.0)箇、(125.3±7.5)箇和(37.3±8.6)箇,陰性對照組和FOXM1 siRNA轉染組的集落形成抑製率分彆為(7.40±0.94)%和(72.40±6.09)%(P<0.05).FOXM1 siRNA轉染組的G2/M期細胞比例為(55.60±4.83)%,明顯高于空白組[(24.30±1.95)%]和陰性對照組[(21.30±2.06)%,P<0.05].轉染FOXM1 siRNA後,可明顯增加A549細胞對AG1478的藥物敏感性(P<0.05).AG1478可誘導活化的FOXO3a分子錶達併促進其覈定位;轉染FOXO3a siRNA後,FOXM1蛋白水平明顯上調,併通過活化的AKT削弱AG1478對FOXM1錶達的抑製.結論 AG1478通過誘導活化的FOXO3a錶達及胞覈重定位,下調FOXM1的錶達,進而抑製肺癌細胞增殖,增加肺癌細胞對AG1478的敏感性.
목적 탐토표피생장인자수체락안산격매억제제AG1478대비소세포폐암세포중차두전록인자M1 (FOXM1)、차두전록인자O3a(FOXO3a)적표체조공,이급RNA간우기술하조FOXM1、FOXO3a적표체후대폐암세포증식급기대AG1478약물민감성적영향.방법 채용역전록취합매련반응(RT-PCR)화Western blot법검측폐선암세포주A549중FOXM1화FOXO3a mRNA화단백적표체정황;순시전염FOXM1화FOXO3a소간우RNA (siRNA)후,RT-PCR화Western blot법검측전염효솔화상관단백적표체;채용CCK-8법、집락형성실험화류식세포의분별검측세포증식、집락형성능력급세포주기분포적개변.결과 AG1478정시간의뢰성억제FOXM1 mRNA화단백적표체(균P<0.05).전염FOXM1 siRNA후,FOXM1 mRNA화단백급기세포주기단백B1(cyclin B1)、c-Myc、Bcl-2단백적표체명현하강,p21화전절후다선감이린산핵당취합매(cleaved-PARP)단백적표체칙명현상조(균P <0.05).공백조、음성대조조화FOXM1 siRNA전염조적집락수분별위(135.3±7.0)개、(125.3±7.5)개화(37.3±8.6)개,음성대조조화FOXM1 siRNA전염조적집락형성억제솔분별위(7.40±0.94)%화(72.40±6.09)%(P<0.05).FOXM1 siRNA전염조적G2/M기세포비례위(55.60±4.83)%,명현고우공백조[(24.30±1.95)%]화음성대조조[(21.30±2.06)%,P<0.05].전염FOXM1 siRNA후,가명현증가A549세포대AG1478적약물민감성(P<0.05).AG1478가유도활화적FOXO3a분자표체병촉진기핵정위;전염FOXO3a siRNA후,FOXM1단백수평명현상조,병통과활화적AKT삭약AG1478대FOXM1표체적억제.결론 AG1478통과유도활화적FOXO3a표체급포핵중정위,하조FOXM1적표체,진이억제폐암세포증식,증가폐암세포대AG1478적민감성.
Objective To explore the effects of EGFR-TKI AG1478 on the expression of FoxM1 and FOXO3a genes in non-small cell cancer (NSCLC) cell lines,and explore the effect on cell proliferation and drug sensitivity to AG1478 after down-regulation of FOXM1 and FOXO3a expression by RNAi technique.Methods Human lung cancer cells were treated with AG1478 at different concentrations.RT-PCR and Western blot were used to examine the expression of P-EGFR,FOXM1,FOXO3a mRNA and protein.After transient transfection of FOXM1 and FOXO3a siRNA,RT-PCR and Western blot were employed to determine the transfection efficiency and expression of the related proteins.CCK-8 assay,colony formation assay and flow cytometry were performed to evaluate the cell proliferation,colony formation ability and the changes in cell cycle distribution.Results The expressions of FOXM1 mRNA and protein were inhibited by AG1478 in a dose-dependent manner (both P < 0.05).After transfection with FOXM1 siRNA,the expressions of FOXM1 mRNA and protein,and proteins of cyclin B1,c-Myc,and Bcl-2 were significantly down-regulated,and the expressions of p21 and cleaved-PARP proteins were significantly up-regulated (all P < 0.05).The colony number of FOXM1 siRNA transfection group was 37.3 ± 8.6,significantly lower than that of the blank control (135.3 ± 7.0) and negative control group (125.3 ± 7.5,P < 0.05).The colony formation inhibition rate was (7.40 ±0.94)% in the negative control group and (72.4 ±6.09)% in the FOXM1 siRNA transfection group.FOXM1siRNA transfection induced cell cycle arrest at G2/M phase with a percentage of (55.6 ± 4.83) %,significantly higher than that of the blank control [(24.30 ± 1.95) %]and negative control group [(21.3 ± 2.06) %,P < 0.05].Additionally,the FOXM1 siRNA transfection significantly increased the chemosensitivity of A549 cells to AG1478 (P < 0.05).Besides,AG1478 induced expression and nuclear relocation of FOXO3a.After the FOXO3a siRNA transfection,the expression of FOXM1 protein was significantly up-regulated,and resulted in a reduction of AG1478-induced inhibition of FOXM1.Conclusions The expression of FOXM1 is down-regulated by AG1478 via FOXO3a in the NSCLC cell lines,and then increases the chemosensitivity of A549 cells to AG1478.It suggests that FOXM1 could be a potential target for the therapy and drug exploitation for NSCLC.