Dioscorea nipponica Attenuates Migration and Invasion by Inhibition of Urokinase-Type Plasminogen Activator through Involving PI3K/Akt and Transcriptional Inhibition of NF-κB and SP-1 in Hepatocellular Carcinoma

污渍 蛋白激酶B 癌症研究 PI3K/AKT/mTOR通路 尿激酶受体 免疫印迹 转移 分子生物学 纤溶酶原激活剂 庆大霉素保护试验 酶谱 细胞迁移 LY294002型 生物 激活剂(遗传学) 化学 信号转导 基质金属蛋白酶 细胞 癌症 细胞生物学 基因 内分泌学 生物化学 遗传学
作者
Ming‐Ju Hsieh,Chao‐Bin Yeh,Hui‐Ling Chiou,Ming‐Chang Hsieh,Shun‐Fa Yang
出处
期刊:The American Journal of Chinese Medicine [World Scientific]
卷期号:44 (01): 177-195 被引量:10
标识
DOI:10.1142/s0192415x16500129
摘要

High mortality and morbidity rates for hepatocellular carcinoma (HCC) in Taiwan primarily result from uncontrolled tumor metastasis. In our previous studies, we have reported that Dioscorea nipponica Makino extract (DNE) has anti-metastasis effects on human oral cancer cells. However, the effect of DNE on hepatoma metastasis have not been thoroughly investigated and remains poorly understood. To determine the effects of DNE on the migration and invasion in HCC cells we used a wound healing model, Boyden chamber assays, gelatin/casein zymography and Western blotting. Transcriptional levels of matrix metalloproteinase-9 (MMP-9) and urokinase-type plasminogen activator (u-PA) were detected by real-time PCR and promoter assays. In this study, DNE treatment significantly inhibited the migration/invasion capacities of Huh7 cell lines. The results of gelatin/casein zymography and Western blotting revealed that the activities and protein levels of the MMP-9 and u-PA were inhibited by DNE. Tests of the mRNA levels, real-time PCR, and promoter assays evaluated the inhibitory effects of DNE on u-PA expression in human hepatoma cells. A chromatin immunoprecipitation (ChIP) assay showed not only that DNE inhibits u-PA expression, but also the inhibitory effects were associated with the down-regulation of the transcription factors of NF-[Formula: see text]B and SP-1 signaling pathways. Western blot analysis also showed that DNE inhibits PI3K and phosphorylation of Akt. In conclusion, these results show that u-PA expression may be a potent therapeutic target in the DNE-mediated suppression of HCC invasion/migration. DNE may have potential use as a chemo-preventive agent against liver cancer metastasis.
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