中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2009年
8期
1028-1030
,共3页
张玉宝%张玉和%李兵%张岂凡
張玉寶%張玉和%李兵%張豈凡
장옥보%장옥화%리병%장기범
乳腺癌%腺病毒%p53基因%耐药性
乳腺癌%腺病毒%p53基因%耐藥性
유선암%선병독%p53기인%내약성
Breast carcinoma%Adenocarcinoma%p53 gene%Drug resistance
目的 探讨野生型p53基因对乳腺癌耐药细胞株MCF-7/A耐药性的逆转作用及其机制.方法 选用含野生型p53基因的重组腺病毒载体,转染乳腺癌耐药细胞株MCF-7/A,绘制细胞生长曲线,利用流式细胞计数仪检测细胞周期分布及凋亡分析、TUNEL法检测细胞凋亡的发生,并采用逆转录-聚合酶链反应(RT-PCR)和Western blot印迹转移检测p53基因的表达情况.结果 野生型p53基因转染MCF-7/A后的24、48 h均检测到p53基因的表达,并显著抑制MCF-7/A细胞的增殖;细胞周期发生改变,转染后的MCF-7/A的G0%G1期DNA百分含量(76.22%)明显高于对照组(43.64%,P<0.05),凋亡率(10.76%)与对照组(1.48%)之间差异有统计学意义(P<0.05).结论 重组腺病毒介导的野生型p53基因对乳腺癌耐药细胞株MCF-7/A的耐药性有明显的逆转作用,其机制可能是引起明显的G1期阻滞并诱导细胞凋亡.
目的 探討野生型p53基因對乳腺癌耐藥細胞株MCF-7/A耐藥性的逆轉作用及其機製.方法 選用含野生型p53基因的重組腺病毒載體,轉染乳腺癌耐藥細胞株MCF-7/A,繪製細胞生長麯線,利用流式細胞計數儀檢測細胞週期分佈及凋亡分析、TUNEL法檢測細胞凋亡的髮生,併採用逆轉錄-聚閤酶鏈反應(RT-PCR)和Western blot印跡轉移檢測p53基因的錶達情況.結果 野生型p53基因轉染MCF-7/A後的24、48 h均檢測到p53基因的錶達,併顯著抑製MCF-7/A細胞的增殖;細胞週期髮生改變,轉染後的MCF-7/A的G0%G1期DNA百分含量(76.22%)明顯高于對照組(43.64%,P<0.05),凋亡率(10.76%)與對照組(1.48%)之間差異有統計學意義(P<0.05).結論 重組腺病毒介導的野生型p53基因對乳腺癌耐藥細胞株MCF-7/A的耐藥性有明顯的逆轉作用,其機製可能是引起明顯的G1期阻滯併誘導細胞凋亡.
목적 탐토야생형p53기인대유선암내약세포주MCF-7/A내약성적역전작용급기궤제.방법 선용함야생형p53기인적중조선병독재체,전염유선암내약세포주MCF-7/A,회제세포생장곡선,이용류식세포계수의검측세포주기분포급조망분석、TUNEL법검측세포조망적발생,병채용역전록-취합매련반응(RT-PCR)화Western blot인적전이검측p53기인적표체정황.결과 야생형p53기인전염MCF-7/A후적24、48 h균검측도p53기인적표체,병현저억제MCF-7/A세포적증식;세포주기발생개변,전염후적MCF-7/A적G0%G1기DNA백분함량(76.22%)명현고우대조조(43.64%,P<0.05),조망솔(10.76%)여대조조(1.48%)지간차이유통계학의의(P<0.05).결론 중조선병독개도적야생형p53기인대유선암내약세포주MCF-7/A적내약성유명현적역전작용,기궤제가능시인기명현적G1기조체병유도세포조망.
Objective To explore the reverse effect of Wt-p53 gene on drug resistance of breast cancer cell line MCF-7/A and its possible mechanism.Methods Wt-p53 gene was tranfected into MCF-7/A cells through rebuilding adenovirus.The cell growth curve was drawn, and the cycle distribution and apoptosis were checked by FCM.The apoptosis of MCF-7/A cells was examined by TUNEL.The expression of Wt-p53 mRNA and protein in MCF-7/A cells was detected by PT-PCR and Western blot respec-tively.Results In the transfection group of MCF-7/A cells, there was obvious proliferation, and the expression of p53 mRNA and protein was detected 24 and 48 h later.Aneuploid peak before G, stage indicated DNA destruction and cell apoptosis.The DNA content in transfection group in G0-G1 stage (76.22%) was significantly higher than control group (43.64%) (P < 0.05).The TUNEL verified that there was an apparent apoptosis signal in which the apoptosis rate of transfected MCF-7/A was 10.76% ,while that was 1.48% in control group (P < 0.05).Conclusion Recombinant adenovirus-mediated Wt-p53 has an apparently reverse effect on drug resistance of breast cancer MCF-7/A cells by inducing cell apoptosis and apparent G1 stage arrest.