中国医科大学学报
中國醫科大學學報
중국의과대학학보
JOURNAL OF CHINA MEDICAL UNIVERSITY
2010年
9期
727-729,736
,共4页
孙秀华%胡海洋%张洪开%解智慧%于爱鸣
孫秀華%鬍海洋%張洪開%解智慧%于愛鳴
손수화%호해양%장홍개%해지혜%우애명
胰岛素样生长因子1%肺癌%S期激酶相关蛋白2%CDC20同源蛋白1%细胞增殖
胰島素樣生長因子1%肺癌%S期激酶相關蛋白2%CDC20同源蛋白1%細胞增殖
이도소양생장인자1%폐암%S기격매상관단백2%CDC20동원단백1%세포증식
insulin-like growth factor -1%lung cancer%SKP2%CDC20 homolog 1%cell proliferation
目的探讨胰岛素样生长因子1(IGF-1)对人非小细胞肺癌(NSCLC)细胞增殖的影响及可能的分子机制。方法 MTT比色法检测0.1,1,10,100 ng/ml IGF-1对非小细胞肺癌系腺癌A549、鳞癌LK2、大细胞肺癌H460细胞增殖的影响,流式细胞术(FCM)、Western blot分析IGF-1处理前后各肺癌细胞的细胞周期变化,S期激酶相关蛋白2(SKP2)和CDC20同源蛋白1(CDH1)的表达变化。结果在非小细胞肺癌系A549、LK2、H460中,不同浓度的IGF-1均显示有促进细胞增殖的作用(P〈0.05),其中1 ng/ml IGF-1作用后细胞增殖率达到峰值;与DMSO组相比,处理组S期细胞增加(P〈0.01),SKP2蛋白表达增加(P〈0.05),但CDH1蛋白表达却无明显变化(P〉0.05)。结论非小细胞肺癌细胞中IGF-1可能是通过SKP2蛋白表达的增强,负性调控p27作用,加速细胞周期的进程。
目的探討胰島素樣生長因子1(IGF-1)對人非小細胞肺癌(NSCLC)細胞增殖的影響及可能的分子機製。方法 MTT比色法檢測0.1,1,10,100 ng/ml IGF-1對非小細胞肺癌繫腺癌A549、鱗癌LK2、大細胞肺癌H460細胞增殖的影響,流式細胞術(FCM)、Western blot分析IGF-1處理前後各肺癌細胞的細胞週期變化,S期激酶相關蛋白2(SKP2)和CDC20同源蛋白1(CDH1)的錶達變化。結果在非小細胞肺癌繫A549、LK2、H460中,不同濃度的IGF-1均顯示有促進細胞增殖的作用(P〈0.05),其中1 ng/ml IGF-1作用後細胞增殖率達到峰值;與DMSO組相比,處理組S期細胞增加(P〈0.01),SKP2蛋白錶達增加(P〈0.05),但CDH1蛋白錶達卻無明顯變化(P〉0.05)。結論非小細胞肺癌細胞中IGF-1可能是通過SKP2蛋白錶達的增彊,負性調控p27作用,加速細胞週期的進程。
목적탐토이도소양생장인자1(IGF-1)대인비소세포폐암(NSCLC)세포증식적영향급가능적분자궤제。방법 MTT비색법검측0.1,1,10,100 ng/ml IGF-1대비소세포폐암계선암A549、린암LK2、대세포폐암H460세포증식적영향,류식세포술(FCM)、Western blot분석IGF-1처리전후각폐암세포적세포주기변화,S기격매상관단백2(SKP2)화CDC20동원단백1(CDH1)적표체변화。결과재비소세포폐암계A549、LK2、H460중,불동농도적IGF-1균현시유촉진세포증식적작용(P〈0.05),기중1 ng/ml IGF-1작용후세포증식솔체도봉치;여DMSO조상비,처리조S기세포증가(P〈0.01),SKP2단백표체증가(P〈0.05),단CDH1단백표체각무명현변화(P〉0.05)。결론비소세포폐암세포중IGF-1가능시통과SKP2단백표체적증강,부성조공p27작용,가속세포주기적진정。
Objective To investigate the effects of insulin-like growth factor-1(IGF-1)on the cell proliferation of human non-small-cell lung cancer(NSCLC) and the possible molecular mechanism.Methods MTT assay was used to examine the effects of IGF-1 (0.1,1,10,100 ng/mL)on the cell proliferation of NSCLC cell lines(A549,LK2,H460),Flow cytometry(FCM)and Western blot to ana-lyze the cell cycles and the protein expression of S-Phase Kinase-Associated Proteins 2(Skp2)and CDC20 homolog 1(CDH1),respectively.Results The cell proliferation of NSCLC cell lines(A549,LK2,H460)could be promoted by the IGF-1 at different concentrations and the proliferation rate peaked when the cells were treated with 1 ng/mL IGF-1.Compared with control,the percentage of the S-phase cell population was significantly increased after the treatment of IGF-I(P 〈 0.01)and the protein expression of SKP2 also increased obviously(P 〈0.05).However,there was no change in the CDH1 protein expression(P 〉 0.05).Conclusion IGF-1 may accelerate the cell-cycle pro-gression of NSCLC cells by negatively modulating p27 protein via the up-regulation of SKP2 protein expression.