Kong Heng, Huang Zong-hai, Chen Hai-jin, Li Qiang, Tao Lin-yu, Qi Ke
Department of Breast and Thyroid Surgery, Sixth Hospital of Shenzhen, Shenzhen, 510282, China. generaldoc@ 126.com
Nan Fang Yi Ke Da Xue Xue Bao. 2010 Jan;30(1):47-50.
To study the selective cytotoxic effect of lentivirus-mediated double suicide gene (CD/TK) against human gastric carcinoma cells SGC-7901 in vitro.
SGC-7901 cells were infected with FGW-KDRP-CD/TK vector and the infection efficiency was observed under a fluorescence microscope. The morphological changes of the infected cells were observed by Giemsa staining. Flow cytometry (FCM) was employed for cell cycle analysis, and the expression of CD/TK was detected by RT-PCR. The infected cells were then treated with the prodrugs ganciclovir (GCV) and/or 5-fluorocytosine (5-FC) at different concentrations, and the cytotoxic effects were evaluated using MTT method.
The infection efficiency of the lentiviral vector in SGC-7901 cells increased with the titer of the virus, which produced no significant effect on the cancer cell morphology in vitro or on the percentages of G0-G1, G2-M and S phase cells (P>0.05). RT-PCR demonstrated the expression of CD/TK gene in SGC-7901 cells infected by FGW-KDRP-CD/TK. The infected cells were highly sensitive to the prodrugs with a dose-dependent cytotoxic effect within a specific concentration range of the drugs, whereas the non-infected cells were not sensitive to the prodrugs. Combined use of the two prodrugs produced an obviously stronger inhibitory effect than either of the them (P<0.05). When combined, GCV and 5-FC at the concentration of 0.1+40, 1+80, 10+160, and 100+320 mg/L demonstrated a synergetic effect with a CDI<1.
Lentivirus-mediated CD/TK fusion gene system can selectively kill gastric cancer cells, and the two prodrugs show a synergistic cytotoxic effect.
研究慢病毒介导的双自杀基因(CD/TK)对人胃癌细胞SGC - 7901的体外选择性细胞毒作用。
用FGW - KDRP - CD/TK载体感染SGC - 7901细胞,在荧光显微镜下观察感染效率。吉姆萨染色观察感染细胞的形态变化。采用流式细胞术(FCM)进行细胞周期分析,RT - PCR检测CD/TK的表达。然后用不同浓度的前体药物更昔洛韦(GCV)和/或5 - 氟胞嘧啶(5 - FC)处理感染细胞,采用MTT法评估细胞毒作用。
慢病毒载体在SGC - 7901细胞中的感染效率随病毒滴度增加而升高,对体外癌细胞形态及G0 - G1、G2 - M和S期细胞百分比无显著影响(P>0.05)。RT - PCR证实FGW - KDRP - CD/TK感染的SGC - 7901细胞中有CD/TK基因表达。感染细胞对前体药物高度敏感,在药物特定浓度范围内具有剂量依赖性细胞毒作用,而未感染细胞对前体药物不敏感。两种前体药物联合使用产生的抑制作用明显强于单独使用(P<0.05)。联合使用时,浓度为0.1 + 40、1 + 80、10 + 160和100 + 320 mg/L的GCV和5 - FC表现出协同作用,CDI<1。
慢病毒介导的CD/TK融合基因系统可选择性杀伤胃癌细胞,两种前体药物表现出协同细胞毒作用。