摘要
研究p53反义RNA对大肠癌细胞中突变型p53致癌性的抑制效应,为肿瘤基因治疗提供新思路。方法2.1kb的人p53全长cDNA反向插入哺乳动物表达载体pREP9,得到p53反义RNA表达载体pREP9-p53(AS),并将其导入人肠癌细胞株SW1116(内源性突变型p53),采用MTT和FCM方法测定pREP9-p53(AS)表达的p53反义RNA对SW1116细胞生长的影响。结果带有pREP9-p53(AS)的SW1116细胞,与对照组SW1116细胞和带pREP9空载体的SW1116细胞相比,由于p53反义RNA的表达,其增殖速度显著下降,FCM的结果也证明带pREP9-p53(AS)的细胞部分受阻于G0/1期,而带pREP9空载体的细胞则无明显变化。结论p53反义RNA可以有效地抑制大肠癌细胞中突变型p53的致癌性。
Objective Inhibition effect ofp53 antisense RNA on malignant phenotype of colorec-tal cancer cells wals studied.Methods For the purpose of inhibiting tumorigenecity of mutant p53 gene in colorectal cancer cells,a 2.1kb human p53 full length cDNA was inserted into a mammalian expression vector pREP9 to make a p53 antisense RNA expression vector pREP9-53(AS).pREP9-p53(AS) was then introduced into human colorectal cancer cell line SW1116(with mutated endoge-nous p53). MTT method and FCM analysis were performed to measure the effect of p53 antisense RNA expressed by pREP9-p53(AS)on SW1116 cell cycle progression.Results and conclusion It was shown that the growth rate of SW1116 cells with pREP-p53(AS) was significantly suppressed by the cxpressionof p53 antisense RNA as compared to the control SW1116 cells andSW1116 cells with pREP9 vector alone.FCM analysis showed that SW1116 cells with pREP-p53(AS) were ar-rested at C o/1 phase,whereas no significant influence can be observed on control SW1116 cells with pREP9.
出处
《中华肿瘤杂志》
CAS
CSCD
北大核心
1997年第2期123-126,共4页
Chinese Journal of Oncology
基金
国家"八五"攻关项目基金