Chen Jun, Ding Wu-Hua, Xu Shao-Yong, Wang Jia-Ning, Huang Yong-Zhang, Deng Chang-Sheng
Department of Gastroenterology, Affiliated People's Hospital of Yunyang Medical College, Shiyan, Hubei Province, China.
World J Gastroenterol. 2009 Jun 14;15(22):2794-9. doi: 10.3748/wjg.15.2794.
To construct p27mt recombinant adenovirus, transfect the colorectal cell line Lovo and observe the effects of p27mt on Lovo cell apoptosis and cell cycle inhibition.
We constructed recombinant adenovirus containing p27mt by homologous recombination in bacteria. The colorectal cancer cell line Lovo was infected with recombinant replication-defective adenovirus Ad-p27mt, and expression of p27mt was determined by Western blotting; the inhibitory effect of p27mt on Lovo cells was detected by cytometry. Cell cycle was determined by flow cytometry. DNA fragment analysis identified the occurrence of apoptosis.
The recombinant adenovirus which already contained p27mt target gene was successfully constructed. When multiplicity of infection was >or= 50, the infection efficiency was 100%. After transfection of Lovo cells with Ad-p27mt the cells had high p27 expression which was identified by immunoblotting assay. PI staining and flow cytometry showed that 77.96% of colorectal cancer cells were inhibited in phase G(0)/G(1), while in the Ad-LacZ group and blank control group, 27.57% and 25.29% cells were inhibited in the same phase, respectively. DNA fragment analysis, flow cytometry and TUNEL assay demonstrated that p27mt is able to induce apoptosis in colorectal cancer cells.
p27mt has an obvious blocking effect on colorectal cancer cell cycle, and most cells were inhibited in phase G(0)/G(1). Therefore, p27mt can induce apoptosis in colorectal cells.
构建p27mt重组腺病毒,转染大肠癌细胞系Lovo,观察p27mt对Lovo细胞凋亡及细胞周期抑制的影响。
通过细菌内同源重组构建含p27mt的重组腺病毒。用重组复制缺陷型腺病毒Ad-p27mt感染大肠癌细胞系Lovo,采用蛋白质免疫印迹法检测p27mt的表达;用细胞计数法检测p27mt对Lovo细胞的抑制作用。采用流式细胞术检测细胞周期。通过DNA片段分析鉴定细胞凋亡的发生。
成功构建了含p27mt目的基因的重组腺病毒。当感染复数≥50时,感染效率为100%。用Ad-p27mt转染Lovo细胞后,经免疫印迹分析证实细胞有高表达的p27。PI染色和流式细胞术显示,77.96%的大肠癌细胞被阻滞于G(0)/G(1)期,而在Ad-LacZ组和空白对照组中,分别有27.57%和25.29%的细胞被阻滞于同一期。DNA片段分析、流式细胞术和TUNEL检测表明,p27mt能够诱导大肠癌细胞凋亡。
p27mt对大肠癌细胞周期有明显的阻滞作用,多数细胞被阻滞于G(0)/G(1)期。因此,p27mt可诱导大肠癌细胞凋亡。