中国病理生理杂志
中國病理生理雜誌
중국병리생리잡지
CHINESE JOURNAL OF PATHOPHYSIOLOGY
2014年
6期
982-987
,共6页
张文峰%贾筠%吴凤麟%沈晗%邵红伟%黄树林
張文峰%賈筠%吳鳳麟%瀋晗%邵紅偉%黃樹林
장문봉%가균%오봉린%침함%소홍위%황수림
细胞凋亡%乳腺肿瘤%存活蛋白
細胞凋亡%乳腺腫瘤%存活蛋白
세포조망%유선종류%존활단백
Apoptosis%Breast neoplasms%Survivin-2B
目的:探讨存活蛋白2B ( survivin-2B)在诱导肿瘤细胞凋亡中的分子机制。方法:将survivin-2B基因插入真核表达载体pCDNA3.1,得到重组载体pCDNA3.1-survivin-2B。将空载体pCDNA3.1及重组载体pCD-NA3.1-survivin-2B分别转染人乳腺癌细胞株MCF7,转染后48 h,用annexin V/7-AAD染色法分析细胞凋亡情况,利用碘化丙啶染色法分析转染对细胞周期的影响;同时提取总RNA并反转录成cDNA,进行多重聚合酶链反应。利用GeXP多基因表达分析系统检测21个与肿瘤相关基因的表达情况。结果:过表达survivin-2B基因导致MCF7细胞凋亡与细胞周期阻滞,并引起8个基因表达上调,2个基因表达下调。变化最大的为醛脱氢酶4家族成员A1(ALDH4A1),表达下降48%;变化最小的为胞质分裂调控蛋白1(PRC1),上调1.08倍。结论: Survivin-2B能够诱导细胞凋亡与细胞周期G2/M期阻滞,并引起部分肿瘤相关基因的表达变化。
目的:探討存活蛋白2B ( survivin-2B)在誘導腫瘤細胞凋亡中的分子機製。方法:將survivin-2B基因插入真覈錶達載體pCDNA3.1,得到重組載體pCDNA3.1-survivin-2B。將空載體pCDNA3.1及重組載體pCD-NA3.1-survivin-2B分彆轉染人乳腺癌細胞株MCF7,轉染後48 h,用annexin V/7-AAD染色法分析細胞凋亡情況,利用碘化丙啶染色法分析轉染對細胞週期的影響;同時提取總RNA併反轉錄成cDNA,進行多重聚閤酶鏈反應。利用GeXP多基因錶達分析繫統檢測21箇與腫瘤相關基因的錶達情況。結果:過錶達survivin-2B基因導緻MCF7細胞凋亡與細胞週期阻滯,併引起8箇基因錶達上調,2箇基因錶達下調。變化最大的為醛脫氫酶4傢族成員A1(ALDH4A1),錶達下降48%;變化最小的為胞質分裂調控蛋白1(PRC1),上調1.08倍。結論: Survivin-2B能夠誘導細胞凋亡與細胞週期G2/M期阻滯,併引起部分腫瘤相關基因的錶達變化。
목적:탐토존활단백2B ( survivin-2B)재유도종류세포조망중적분자궤제。방법:장survivin-2B기인삽입진핵표체재체pCDNA3.1,득도중조재체pCDNA3.1-survivin-2B。장공재체pCDNA3.1급중조재체pCD-NA3.1-survivin-2B분별전염인유선암세포주MCF7,전염후48 h,용annexin V/7-AAD염색법분석세포조망정황,이용전화병정염색법분석전염대세포주기적영향;동시제취총RNA병반전록성cDNA,진행다중취합매련반응。이용GeXP다기인표체분석계통검측21개여종류상관기인적표체정황。결과:과표체survivin-2B기인도치MCF7세포조망여세포주기조체,병인기8개기인표체상조,2개기인표체하조。변화최대적위철탈경매4가족성원A1(ALDH4A1),표체하강48%;변화최소적위포질분렬조공단백1(PRC1),상조1.08배。결론: Survivin-2B능구유도세포조망여세포주기G2/M기조체,병인기부분종류상관기인적표체변화。
AIM:To explore the role of survivin-2B in the process of tumor cell apoptosis .METHODS:The survivin-2B gene was cloned into pcDNA3.1 vector and the recombinant plasmid pcDNA3.1-survivin-2B was obtained.Hu-man breast cancer MCF7 cells were transfected with pcDNA3.1 and pcDNA3.1-survivin-2B using Lipofectamine 2000.The cell cycle was determined by propidium iodide staining , and the apoptosis was detected by annexin V/7-AAD staining 48 h after transfection.Meanwhile, tatal RNA was extrated and multiplex polymerase chain reaction based on GenomeLab GeXP Genetic Analysis System was performed to detect the expression of 21 tumor-related genes .RESULTS: Flow cytometry analysis indicated that over-expression of survivin-2B promoted the apoptosis and cell cycle arrest of MCF 7 cells.Compared with control group , totally 10 differential expressed genes were related to the over-expressed survivin-2B, among which 2 were up-regulated and 8 were down-regulated. The expression of aldehyde dehydrogenase 4 family member A1 (ALDH4A1) was 48%down-regulated, and the expression of protein regulator of cytokinesis 1 (PRC1) was 1.08 folds up-regulated.CONCLUSION:Survivin-2B induces the expression changes of some tumor-related genes, which results in the apoptosis and G 2/M arrest of MCF7 cells.