Activation of Multiple Apoptotic Pathways in Human Nasopharyngeal Carcinoma Cells by the Prenylated Isoflavone, Osajin

NCUIR > college of Health Sciences and Technology > Department of Life Science > journal & Dissertation > Item 987654321/50788

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/50788

Title:	Activation of Multiple Apoptotic Pathways in Human Nasopharyngeal Carcinoma Cells by the Prenylated Isoflavone, Osajin
Authors:	Huang,TT;Liu,FG;Wei,CF;Lu,CC;Chen,CC;Lin,HC;Ojcius,DM;Lai,HC
Contributors:	生命科學系
Keywords:	ENDOPLASMIC-RETICULUM STRESS;MACLURA-POMIFERA;CANCER;DEATH;BCL-2;TUMOR;FLAVONOIDS;INDUCTION;LINES;BAX
Date:	2011
Issue Date:	2012-03-27 18:10:10 (UTC+8)
Publisher:	國立中央大學
Abstract:	Osajin is a prenylated isoflavone showing antitumor activity in different tumor cell lines. The underlying mechanism of osajin-induced cancer cell death is not clearly understood. In the present study, the mechanisms of osajin-induced cell death of human nasopharyngeal carcinoma (NPC) cells were explored. Osajin was found to significantly induce apoptosis of NPC cells in a dose-and time-dependent manner. Multiple molecular effects were observed during osajin treatment including a significant loss of mitochondrial transmembrane potential, release of cytochrome c into the cytosol, enhanced expression of Fas ligand (FasL), suppression of glucose-regulated protein 78 kDa (GRP78), and activation of caspases-9, -8, -4 and -3. In addition, up-regulation of proapoptotic Bax protein and down-regulation of antiapoptotic Bcl-2 protein were also observed. Taken together, osajin induces apoptosis in human NPC cells through multiple apoptotic pathways, including the extrinsic death receptor pathway, and intrinsic pathways relying on mitochondria and endoplasmic reticulum stress. Thus, osajin could be developed as a new effective and chemopreventive compound for human NPC.
Relation:	PLOS ONE
Appears in Collections:	[Department of Life Science] journal & Dissertation

Files in This Item:

File	Description	Size	Format
index.html		0Kb	HTML	862	View/Open

社群 sharing

Loading...