Docosahexaenoic acid inhibits lipopolysaccharide-induced metastatic activities by decreasing inflammation on prostate cancer cell.

Zhengping Wu, Chung-Yi Chen, C. Kao, Yi-Hai Jiang, Chi-Ming Liu
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引用次数: 2

Abstract

Docosahexaenoic acid (DHA) is rich in fish oil with many pharmacological impacts such as anti-inflammation and anti-cancer activities. In the present study, we aimed to investigate the inhibitory effects of DHA on the invasion and inflammation in prostate cancer cells. The cytotoxicity of DHA with or without lipopolysaccharides (LPS) treatment was evaluated by MTT assay. The invasion and wound healing assays were used to determine the roles of DHA in cell migration and invasion after LPS treatment. The expression levels of IL-6 and IL-8 were detected using ELISA assay. The protein expression was investigated by Western blotting. DHA exhibited significant cytotoxicity at the concentration of 100 μM in PC3 cells. Exposure to DHA (6, 12 and 25 μM) dose-dependently inhibited invasion and wound closure potential in PC3 cells after LPS treatment. DHA dose-dependently downregulated LPS-induced expression levels of IL-6 and IL-8. In addition, the LPS-induced protein levels of p-AKT and COX-2 were suppressed by DHA treatment. Our results indicate that low doses of DHA effectively inhibit metastasis by decreasing IL-6, IL-8, p-AKT and COX-2 expression levels after LPS treatment.
二十二碳六烯酸通过降低前列腺癌细胞的炎症来抑制脂多糖诱导的转移活性。
鱼油中含有丰富的二十二碳六烯酸(DHA),具有抗炎、抗癌等药理作用。在本研究中,我们旨在研究DHA对前列腺癌细胞侵袭和炎症的抑制作用。采用MTT法评价DHA在脂多糖(LPS)处理或不处理下的细胞毒性。采用侵袭和伤口愈合试验来确定DHA在LPS处理后细胞迁移和侵袭中的作用。ELISA法检测IL-6、IL-8的表达水平。Western blotting检测蛋白表达。DHA在100 μM浓度下对PC3细胞具有明显的细胞毒性。暴露于DHA(6、12和25 μM)剂量依赖性地抑制LPS处理后PC3细胞的侵袭和伤口愈合潜力。DHA剂量依赖性下调lps诱导的IL-6和IL-8的表达水平。此外,DHA处理可抑制lps诱导的p-AKT和COX-2蛋白水平。我们的研究结果表明,低剂量DHA通过降低LPS处理后IL-6、IL-8、p-AKT和COX-2的表达水平有效抑制转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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