馬偕醫學大學機構典藏(MacKay Medical University Institutional Repository):Item 987654321/2811
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 1657/1756
Visitors : 3729031      Online Users : 170
RC Version 5.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Adv. Search
LoginUploadHelpAboutAdminister
MMUIR > College of Medicine > Department of Optometry > Journal >  Item 987654321/2811

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/2811

Title: Nobiletin, a polymethoxylated flavone, inhibits glioma cell growth and migration via arresting cell cycle and suppressing MAPK and Akt pathways
Authors: Lien, Li-Ming;Wang, Meng-Jiy;Chen, Ray-Jade;Chiu, Hou-Chang;Wu, Jia-Lun;8, Ming-Yi Shen;Chou, Duen-Suey;Sheu, Joen-Rong;Lin, Kuan-Hung;Lu, Wan-Jung
Contributors: 視光學系
Date: 2016-02-01
Issue Date: 2025-08-11 14:44:17 (UTC+8)
Abstract: Nobiletin, a bioactive polymethoxylated flavone (5,6,7,8,3(') ,4(') -hexamethoxyflavone), is abundant in citrus fruit peel. Although nobiletin exhibits antitumor activity against various cancer cells, the effect of nobiletin on glioma cells remains unclear. The aim of this study was to determine the effects of nobiletin on the human U87 and Hs683 glioma cell lines. Treating glioma cells with nobiletin (20-100 µm) reduced cell viability and arrested the cell cycle in the G0/G1 phase, as detected using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and propidium iodide (PI) staining, respectively; however, nobiletin did not induce cell apoptosis according to PI-annexin V double staining. Data from western blotting showed that nobiletin significantly attenuated the expression of cyclin D1, cyclin-dependent kinase 2, cyclin-dependent kinase 4, and E2 promoter-binding factor 1 (E2F1) and the phosphorylation of Akt/protein kinase B and mitogen-activated protein kinases, including p38, extracellular signal-regulated kinase, and c-Jun N-terminal kinase. Our data also showed that nobiletin inhibited glioma cell migration, as detected by both functional wound healing and transwell migration assays. Altogether, the present results suggest that nobiletin inhibits mitogen-activated protein kinase and Akt/protein kinase B pathways and downregulates positive regulators of the cell cycle, leading to subsequent suppression of glioma cell proliferation and migration. Our findings evidence that nobiletin may have potential for treating glioblastoma multiforme.
Relation: Phtotherapy Reserch, 30, 214-221. https://doi.org/10.1002/ptr.5517
Appears in Collections:[Department of Optometry] Journal

Files in This Item:

File SizeFormat
index.html0KbHTML1View/Open


All items in MMUIR are protected by copyright, with all rights reserved.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback