[SFPS诱导lovo人结直肠癌细胞凋亡及其机制研究]。

Shi yan sheng wu xue bao Pub Date : 2005-10-01
Lin Lin Yan, Qian Liang, Ji Cheng Li
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引用次数: 0

摘要

选择人类结直肠癌(lovo)细胞研究 SFPS 的抗肿瘤作用,并探讨 caspase 3 在 SFPS 诱导 lovo 细胞凋亡中的意义。细胞增殖抑制实验采用 MTT 法。电镜、流式细胞仪和 DNA 电泳观察了 SFPS 诱导的lovo细胞凋亡。此外,还通过 RT-PCR 和 Western 印迹检测了 caspase 3 mRNA 和 pro-caspase 3 的表达。SFPS具有抗增殖活性,且与剂量和时间有关。培养 24、36、48 和 72 h 后,SFPS 对lovo 细胞的 IC50 分别为 375 mg/L、355 mg/L、178 mg/L 和 60 mg/L。琼脂糖凝胶电泳显示,在 5 毫克/升、50 毫克/升和 300 毫克/升的剂量下,SFPS 处理 24 小时后,lovo 细胞的 DNA 梯形显示为 180-200 bp 的完整 DNA 片段。然而,在用 500 毫克/升 SFPS 处理的lovo 细胞中,DNA 梯形图或涂片变得模糊不清。当 SFPS 浓度为 1000 毫克/升时,DNA 梯状结构消失,并完全出现涂片。形态学检查显示染色体缩合、核片边缘化、细胞萎缩和电镜下凋亡体的存在。流式细胞术观察到细胞凋亡和亚 G1 峰,但细胞周期没有明显变化。此外,在时间和剂量依赖性作用下,促caspase 3表达量减少,caspase 3 mRNA水平升高。这表明,SFPS 可诱导体外lovo细胞凋亡,从而抑制其增殖。而caspase 3的激活可能参与了SFPS诱导lovo细胞凋亡的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Study on the apoptosis and its mechanism of lovo human colorectal cancer cells induced by SFPS].

Human colorectal cancer (lovo) cells were chose to study the anti-tumor effects of SFPS and explore the significance of caspase 3 in the apoptosis of lovo cells induced by SFPS. Inhibition of the cell proliferation was measured by MTT assay. SFPS induced apoptosis of lovo cells was observed by electron microscopy, flow cytometry and DNA electrophoresis. Furthermore, the expressions of caspase 3 mRNA and pro-caspase 3 were tested by RT-PCR and Western blot. SFPS exhibited anti-proliferative activity in the dosage and time-dependent manner. After incubation for 24, 36, 48 and 72 h, the IC50 of SFPS on lovo cells was 375 mg/L, 355 mg/L, 178 mg/L and 60 mg/L, respectively. DNA ladders of lovo cells were showed on agarose gel electrophoresis and the fragments of DNA were integral of 180-200 bp 24 hours after SFPS treatment at the doses of 5 mg/L, 50 mg/L and 300 mg/L. However, mistiness DNA ladder or smear was found in lovo cells treated with 500 mg/L SFPS. When SFPS concentration was 1000 mg/l, DNA ladder disappeared and showed smear entirely. Morphological examination showed chromosomal condensation, karyotheca margination, cell shrinkage and the presence of apoptosis bodies with electron microscopy. With concentration dependent manner, the apoptosis and sub-G1 peaks were observed through flow cytometry, but the cell cycle didn't change obviously. Furthermore, the expression of pro-caspase 3 was decreased and the level of caspase 3 mRNA was increased in the time and dose-dependent manner. It suggests that SFPS may induce the apoptosis of lovo cells in vitro resulting in the inhibition of proliferation. And caspase 3 activation may participate in the processes of the apoptosis of lovo cells induced by SFPS.

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