Identification of AR-targeted Active Compounds from Euphorbiahumifusa Willd for the Treatment of Prostate Cancer

山奈酚 化学 雄激素受体 木犀草素 免疫印迹 传统医学 前列腺癌 活力测定 槲皮素 药理学 生物化学 癌症 生物 医学 细胞 抗氧化剂 基因 遗传学
作者
Mireguli Abulimiti,Mourboul Ablise,Jialu Hu,Chengjing Shen,Gulijikere Kuerban,Aikebaier Maimaiti
出处
期刊:Current Cancer Drug Targets [Bentham Science Publishers]
卷期号:25 被引量:1
标识
DOI:10.2174/0115680096359255250420022821
摘要

Introduction: Euphorbia humifusa Willd (EH) is a traditional medicinal herb in China. However, the anti-prostate cancer active compounds of EH and their molecular mechanisms have yet to be elucidated. Methods: The peaks of EH water extract in the fingerprinting were analysed using liquid chromatography coupled to quadrupole time of flight mass spectrometry. The cell viability of 22RV1 cells was determined via MTT. The active compounds and potential targets were screened in silico. The prostate cancer-associated targets were collected from the GeneCards database. The herb-compound-target-disease (H-C-T-D) and PPI networks were constructed to predict key targets. The molecular docking analysis of the active compounds with key targets was conducted using Autodock Vina 1.1.2. Western blot analysis was performed to evaluate the protein expression. Results: LC-MS results demonstrated that EH water extract is a rich source of phenolics and flavonoids. EH water extract inhibited the viability of 22RV1 cells in a time-and dosedependent manner. Moreover, the in silico screening results identified 17 active compounds from EH with 518 prostate cancer-related key genes. Moreover, an H-C-T-D network analysis combined with the PPI network results effectively identified seven chemical compounds, oestrogen receptor 1, and androgen receptor (AR) to be highly related to prostate cancer. Furthermore, molecular docking results showed that 4',5-dihydroxyflavone, ensaculin, luteolin, hypolaetin, quercetin, and kaempferol had a strong binding affinity with AR. Finally, Western blot results demonstrated that EH water extract, quercetin, kaempferol, and luteolin significantly down-regulated the AR protein expression in 22RV1 cells. Conclusion: These results suggest that EH may provide a new promising therapeutic for prostate cancer treatment. .
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