首页> 外文期刊>World journal of gastroenterology : >Inhibitory effect of acetylshikonin on human gastric carcinoma cell line SGC-7901 in vitro and in vivo.
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Inhibitory effect of acetylshikonin on human gastric carcinoma cell line SGC-7901 in vitro and in vivo.

机译:乙酰紫草素在体外和体内对人胃癌细胞SGC-7901的抑制作用。

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AIM: To investigate the inhibitory effect of acetylshikonin on human gastric carcinoma cell line SGC-7901 and its mechanism. METHODS: MTT assay was used to assess the inhibitory effect of acetylshikonin on proliferation of SGC-7901 cells. Apoptosis-inducing effect was determined by flow cytometry and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling with Hoechst staining. Expression of mRNA and protein in Bcl-2 and Bax was analyzed by reverse transcription-polymerase chain reaction and Western blot. Antitumor effect of acetylshikonin on a mouse SGC-7901 model was also determined. RESULTS: Forty-eight hours after treatment with acetylshikonin, MTT assay showed that acetylshikonin inhibited the proliferation of SGC-7901 cells in a dose-dependent manner. The half maximal inhibitory concentration of acetylshikonin to SGC-7901 cells was 0.428 +/- 0.07 mg/L. Cell shrinkage, nuclear pyknosis and chromatin condensation, which are the characteristics of cell apoptosis, were observed in treated SGC-7901 cells and the percentage of apoptosis increased in a dose-dependent manner. Acetylshikonin down-regulated the expression of Bcl-2 and up-regulated the expression of Bax in the treated SGC-7901 cells compared with the controls. The experiment in vivo showed that 0.5, 1, and 2 mg/kg of acetylshikonin significantly inhibited the growth of tumor in the mouse SGC-7901 model, with an inhibitory rate of 25.00%-55.76%. CONCLUSION: Acetylshikonin inhibits the growth of SGC-7901 cells in vitro and in vivo by inducing cell apoptosis.
机译:目的:探讨乙酰紫草素对人胃癌细胞SGC-7901的抑制作用及其机制。方法:采用MTT法评价乙酰紫草素对SGC-7901细胞增殖的抑制作用。通过流式细胞术和末端脱氧核苷酸转移酶介导的Hoechst染色标记的dUTP-生物素缺口末端来确定诱导凋亡的作用。通过逆转录-聚合酶链反应和蛋白质印迹分析Bcl-2和Bax中mRNA和蛋白质的表达。还确定了乙酰紫草素对小鼠SGC-7901模型的抗肿瘤作用。结果:乙酰基紫草苷处理48小时后,MTT分析表明乙酰基紫草苷以剂量依赖性方式抑制SGC-7901细胞的增殖。乙酰紫草素对SGC-7901细胞的最大半数抑制浓度为0.428 +/- 0.07 mg / L。在处理过的SGC-7901细胞中观察到细胞萎缩,核固缩和染色质浓缩是细胞凋亡的特征,并且凋亡百分比以剂量依赖性方式增加。与对照组相比,乙酰基紫草素下调了SGC-7901细胞的Bcl-2表达,并上调了Bax的表达。体内实验表明,在小鼠SGC-7901模型中,0.5、1和2 mg / kg的乙酰基紫草素显着抑制肿瘤的生长,抑制率为25.00%-55.76%。结论:乙酰基紫草苷可通过诱导细胞凋亡来抑制SGC-7901细胞的体内外生长。

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