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作 者:吴孟轩[1]
机构地区:[1]四川省自贡市第三人民医院药剂科,四川自贡643020
出 处:《海南医学院学报》2016年第18期2073-2076,共4页Journal of Hainan Medical University
基 金:四川省卫生厅科研课题(130021)~~
摘 要:目的:研究青蒿素和顺铂联合干预对胃癌MGC-803细胞株上皮间质转化、血管新生及ATP生成的影响。方法:培养胃癌MGC-803细胞株并分为对照组、顺铂组、青蒿素组、顺铂+青蒿素组、顺铂+青蒿素+NAC组、NAC组,给予不同的条件处理后测定细胞活力、凋亡率以及上皮间质转化分子、血管新生分子、ATP的含量。结果:顺铂组、青蒿素组、顺铂+青蒿素组的细胞活力值、ATP生成量以及VEGFA、VEGFB、VEGFC、N-cadherin、Vimentin含量低于对照组,早期凋亡率、晚期凋亡率以及E-cadherin含量高于对照组;顺铂+青蒿素组的细胞活力值、ATP生成量以及VEGFA、VEGFB、VEGFC、N-cadherin、Vimentin含量低于顺铂组和青蒿素组,早期凋亡率、晚期凋亡率以及E-cadherin含量高于顺铂组和青蒿素组。顺铂+青蒿素+NAC组的E-cadherin含量低于顺铂+青蒿素组,ATP生成量以及VEGFA、VEGFB、VEGFC、N-cadherin、Vimentin含量高于顺铂+青蒿素组。结论:青蒿素和顺铂联合干预能够协同发挥对胃癌MGC-803细胞株上皮间质转化、血管新生及ATP生成的抑制效应,该抑制效应部分通过增加活性氧的生成来发挥。Objective: To study the effect of artemisinin combined with cisplatin intervention on epithelial-mesenchymal transition,angiogenesis and ATP generation in MGC-803 gastric cancer cell lines. Methods: MGC-803 gastric cancer cell lines were cultured and divided into control group,cisplatin group,artemisinin group,cisplatin + artemisinin group,cisplatin + artemisinin +NAC group and NAC group,and after different conditions of treatment,cell viability,apoptosis rate as well as levels of epithelial-mesenchymal transition molecules,angiogenesis molecules and ATP were determined. Results: Cell viability,ATP generation as well as VEGFA,VEGFB,VEGFC,N-cadherin and Vimentin levels of cisplatin group,artemisinin group and cisplatin + artemisinin group were lower than those of control group,and early apoptosis rate,late apoptosis rate and E-cadherin levels were higher than those of control group; cell viability,ATP generation as well as VEGFA,VEGFB,VEGFC,N-cadherin and Vimentin levels of cisplatin + artemisinin group were lower than those of cisplatin group and artemisinin group,and early apoptosis rate,late apoptosis rate and E-cadherin level were higher than those of cisplatin group and artemisinin group. E-cadherin level of cisplatin + artemisinin + NAC group was lower than that of cisplatin + artemisinin group,and ATP generation as well as VEGFA,VEGFB,VEGFC,N-cadherin and Vimentin levels were higher than those of cisplatin + artemisinin group. Conclusion: Artemisinin combined with cisplatin intervention cansynergistically exert the inhibitory effect on epithelial-mesenchymal transition,angiogenesis and ATP generation in MGC-803 gastric cancer cell lines,and the inhibiting effect is partially realized by increasing the generation of reactive oxygen species.
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