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作 者:陈道荣[1] 王丕龙[1] 杨雪琴[2] 黄爱龙[3] 张秉强[3] 陶小红[1]
机构地区:[1]重庆医科大学附属第一医院消化内科,重庆400016 [2]重庆市巴南区人民医院消化内科,重庆401320 [3]病毒性肝炎研究所,重庆400010
出 处:《第四军医大学学报》2006年第24期2216-2219,共4页Journal of the Fourth Military Medical University
基 金:国家自然科学基金(30300298);重庆市科委自然科学基金(CSCT2005BB5311)
摘 要:目的:利用RNA干扰(RNAi)技术,以Dnmt1(DNAmethyltransferase1)为靶基因,设计构建重组体pshRNA-Dnmt1,研究其对胃癌AGS细胞增殖凋亡的影响.方法:设计shRNA的寡核苷酸片断,再克隆至载体pTZU6+1中构建重组体pshRNA-Dnmt1,转染胃癌细胞株AGS,用WesternBlot检测DNMT1蛋白水平变化,用RT-PCR法评估mRNA水平,MTT法动态监测活细胞数,AO/EB法、电镜和TUNEL观察其促凋亡作用.结果:成功构建重组质粒pshRNA-Dnmt1后,进行序列分析得到确证.RT-PCR检测结果证实:重组质粒pshRNA-Dnmt1对胃癌AGS细胞中Dnmt1基因的转录有着明显抑制作用,转染后24h抑制率在21.63%左右;48h为52.97%;72h为72.06%.WesternBlot检测结果表明:pshR-NA-Dnmt1转染AGS细胞后24h出现DNMT1蛋白表达量减少,抑制率为28.24%;48h为68.54%;72h为81.47%.MTT结果提示:转染后24,48和72h细胞数存活率为对照组的79.49%,51.63%和39.16%.AO/EB法、电镜和TUNEL都看见大量典型的凋亡和坏死细胞,转染后48h的细胞凋亡率由对照组的5%上升为35%左右.结论:重组质粒pshRNA-Dnmt1能特异有效地抑制胃癌细胞株AGS内Dnmt1基因的表达,能抑制细胞增殖,促进细胞凋亡,从而为肿瘤的基因治疗开辟了新途径.AIM: To design a recombinant plasmid pshRNAdnmtl by RNA interference and to assess its effects on DNA methyltransferase ( Dnmt1 ) gene expression in gastric cancer cell line AGS, and on the proliferation and apoptosis of AGS cells in vitro. METHODS: The eukaryotic expression plasmid pshRNADnmt1, containing the sequence of shRNA, was cloned and transfected into AGS cells. The mRNA levels of gene Dnmtl were determined by RT-PCR, the protein expression levels by Western Blot, the cell survival index by MTT assay, and the apoptosis was also evaluated by AO/EB, electron microscope and TUNEL. RESULTS: A recombinant plasmid pshRNA-Dnmtl was successfully constructed and confirmed by sequencing analysis. PshRNADnmt1 induced a 21.63% inhibition of Dnmtl mRNA after 24 h treatment, 52.97% after 48 h, and 72.06% after 72 h. Dnmtl protein levels in AGS cells appeared to reduce, with inhibition rate of 28.24% after 24 h of treatment, 68.54% after 48 h, and 81.47% after 72 h. MTT results showed that the cell survival rates of AGS cells after transfected with pshRNA-Dnmtl at 24 h, 48 h and 72 h respectively were 79. 49%, 51. 63% and 39.16%. AO/EB, electron microscope and TUNEL test indicated : after transfection with the recombinant plasmid, there existed a lot of apoptotic and necrotic cells, and the apoptosis rate increased from about 5% to 35%. CONCLUSION: The recombinant plasmid pshRNA-Dnmtl can efficiently and specifically inhibit the expression of gene Dnmtl, inhibit the proliferation of AGS cells, and induce the apoptosis.
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