Hyperforin Induces Apoptosis Through Extrinsic/Intrinsic Pathways and Inhibits NF-?B-modulated Survival and Invasion Potential in Bladder Cancer

ASIA unversity > 醫學暨健康學院 > 醫學檢驗暨生物技術學系 > 期刊論文 > Item 310904400/112904

Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/112904

Title:	Hyperforin Induces Apoptosis Through Extrinsic/Intrinsic Pathways and Inhibits NF-?B-modulated Survival and Invasion Potential in Bladder Cancer
Authors:	LIU, YU-CHANG;LIU, YU-CHANG;KUANG-HSUAN;LIN, KUANG-HSUAN;HS, JUNG-HUNG;HSIEH, JUNG-HUNG;鍾景光;TAN, ZHAO-LIN;TAN, ZHAO-LIN;HSU, FEI-TING;HSU, FEI-TING;CH, CHIH-HUNG;CHIANG, CHIH-HUNG
Contributors:	醫學檢驗暨生物技術學系
Keywords:	Hyperforin;NF-κB;apoptosis;bladder cancer;calcium signalling;cytosol ROS;p65.
Date:	2019-11
Issue Date:	2020-09-02 07:52:22 (UTC+0)
Publisher:	亞洲大學
Abstract:	Background/aim: Muscle-invasive bladder cancer (MIBC) has long been recognized as a difficult to treat cancer type, thus a new treatment strategy is needed. The major purpose of the present study was to verify the anticancer effect of hyperforin and the mechanism through which it affects tumor cell growth and invasion in bladder cancer in vitro. Materials and methods: Bladder cancer TSGH-8301 cells were treated with different concentrations of hyperforin for different durations of time. The changes in cell viability, production of calcium and reactive oxygen species (ROS), and anti-apoptotic signaling were evaluated using MTT assay, flow cytometry, and western blot analysis. The effect of hyperforin on the expression of nuclear factor-kappaB (NF-ĸB) p65 (Ser276), tumor progression-associated proteins, as well as on cell invasion was investigated using western blotting and cell invasion assay, respectively. Results: Hyperforin significantly induces apoptosis, extrinsic/intrinsic apoptotic signaling, accumulation of cytosol ROS, and calcium signalling. Hyperforin also significantly diminishes the expression of NF-ĸB p65 (Ser276), anti-apoptotic and tumor progression-associated proteins, as well as the cell invasion ability of TSGH-8301 cells. Conclusion: Our findings demonstrate that hyperforin triggers apoptosis depending on extrinsic/intrinsic pathways and suppresses NF-ĸB-mediated cell survival as well as the invasive properties of bladder cancer in vitro.
Relation:	IN VIVO
Appears in Collections:	[醫學檢驗暨生物技術學系] 期刊論文

Files in This Item:

File	Description	Size	Format
index.html		0Kb	HTML	248	View/Open

View Licence

Loading...