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作 者:史继荣[1] 张翔宇[1] 朱静[1] 乔岐禄[1] 张宝善[1]
出 处:《中国现代医学杂志》2012年第6期14-18,共5页China Journal of Modern Medicine
摘 要:目的研究二十二碳六烯酸(docosahexaenoicacid,DHA)和花生四烯酸(arachidonicacid,从)对人胆囊癌细胞GBC-SD增殖的影响,通过相关蛋白质指标,探讨可能的分子机制。方法MTT法检测不同浓度(10-80ug/mL)DHA和AA对胆囊癌细胞GBC-SD存活率的影响;免疫印迹检测β-catenin、c-myc、cychnD1三种蛋白表达量的变化。结果当DHA浓度达到60ug/mL时可明显抑制胆囊癌细胞GBC-SD存活并随着浓度升高抑制作用增强,呈剂量依赖(P〈o.05),而相同浓度AA无明显作用。同时β-catenin、c-myc、cychnD1三种蛋白表达量均下降。结论DHA可抑制人胆囊癌细胞GBC-SD增殖,使β-catenin、c-myc、cyclinD1表达减少。[ Objective ] To investigate the effect of DHA and AA on human carcinoma of gallbladder cell line cells GBC-SD in vitro and explore possible molecular mechanisms through the relevant protein targets. [ Methods ] GBC-SD cell viability is examined for different concentration (10-80 ug/M1) of DHA and AA by MTI assay. Protein expression of β-catenin, c-myc, cyclin D1 was measured by Western-blot. [Results] The DHA showed a dose de- pendent inhibition to the survival of GBC-SD after the concentration above 60 ug/mL(P 〈0.05). However, there is no significant effect for AA treatment group. The expression of protein β-catenin, c-myc, cyclin D1 are all decreased by western-blot. [ Conclusion ] DHA can effectively inhabit the proliferation of human carcinoma of gallbladder cell line cells GBC-SD, decrease the expression of protein β-catenin, c-myc, cyclin D1.
关 键 词:Ω-3多不饱和脂肪酸 胆囊癌 WNT/Β-CATENIN通路
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