The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells

<p>Abstract</p> <p>Background</p> <p>Previous study reported that resveratrol has anti-tumor activity. In this study, we investigated the involvement of autophagy in the resveratrol-induced apoptotic death of human U251 glioma cells.</p> <p>Methods</p>...

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Main Authors: Qin Zhenghong, Li Jun, Liang Zhongqin
Format: Article
Language:English
Published: BMC 2009-06-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/9/215
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spelling doaj-687a81a8c239467daa5a836f7a87f5902020-11-24T23:27:18ZengBMCBMC Cancer1471-24072009-06-019121510.1186/1471-2407-9-215The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cellsQin ZhenghongLi JunLiang Zhongqin<p>Abstract</p> <p>Background</p> <p>Previous study reported that resveratrol has anti-tumor activity. In this study, we investigated the involvement of autophagy in the resveratrol-induced apoptotic death of human U251 glioma cells.</p> <p>Methods</p> <p>The growth inhibition of U251 cells induced by resveratrol was assessed with methyl thiazolyl tetrazolium (MTT). The activation of autophagy and proapoptotic effect were characterized by monodansylcadaverine labeling and Hoechst stain, respectively. Mitochondrialtransmembrane potential (ΔΨm) was measured as a function of drug treatment using 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolylcarbocyanine iodide (JC-1). The role of autophagy and apoptosis in the resveratrol-induced death of U251 cells was assessed using autophagic and caspase inhibitors. Immunofluorescence, flow cytometry, and Western blot analysis were used to study the apoptotic and autophagic mechanisms.</p> <p>Results</p> <p>Methyl thiazolyl tetrazolium (MTT) assays indicated that resveratrol decreased the viability of U251 cells in a dose- and time-dependent manner. Flow cytometry analysis indicated that resveratrol increased cell population at sub-G1 phase, an index of apoptosis. Furthermore, resveratrol-induced cell death was associated with a collapse of the mitochondrial membrane potential. The pan-caspase inhibitor Z-VAD-fmk suppressed resveratrol-induced U251 cell death. Resveratrol stimulated autophagy was evidenced by punctuate monodansylcadaverine(MDC) staining and microtubule-associated protein light chain 3 (LC3) immunoreactivty. Resveratrol also increased protein levels of beclin 1 and membrane form LC3 (LC3-II). Autophagy inhibitors 3-methylademine (3-MA) and bafilomycin A1 sensitized the cytotoxicity of resveratrol.</p> <p>Conclusion</p> <p>Together, these findings indicate that resveratrol induces autophagy in human U251 glioma cells and autophagy suppressed resveratrol-induced apoptosis. This study thus suggests that autophagy inhibitors can increase the cytotoxicity of resveratrol to glioma cells.</p> http://www.biomedcentral.com/1471-2407/9/215
collection DOAJ
language English
format Article
sources DOAJ
author Qin Zhenghong
Li Jun
Liang Zhongqin
spellingShingle Qin Zhenghong
Li Jun
Liang Zhongqin
The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells
BMC Cancer
author_facet Qin Zhenghong
Li Jun
Liang Zhongqin
author_sort Qin Zhenghong
title The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells
title_short The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells
title_full The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells
title_fullStr The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells
title_full_unstemmed The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells
title_sort prosurvival role of autophagy in resveratrol-induced cytotoxicity in human u251 glioma cells
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2009-06-01
description <p>Abstract</p> <p>Background</p> <p>Previous study reported that resveratrol has anti-tumor activity. In this study, we investigated the involvement of autophagy in the resveratrol-induced apoptotic death of human U251 glioma cells.</p> <p>Methods</p> <p>The growth inhibition of U251 cells induced by resveratrol was assessed with methyl thiazolyl tetrazolium (MTT). The activation of autophagy and proapoptotic effect were characterized by monodansylcadaverine labeling and Hoechst stain, respectively. Mitochondrialtransmembrane potential (ΔΨm) was measured as a function of drug treatment using 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolylcarbocyanine iodide (JC-1). The role of autophagy and apoptosis in the resveratrol-induced death of U251 cells was assessed using autophagic and caspase inhibitors. Immunofluorescence, flow cytometry, and Western blot analysis were used to study the apoptotic and autophagic mechanisms.</p> <p>Results</p> <p>Methyl thiazolyl tetrazolium (MTT) assays indicated that resveratrol decreased the viability of U251 cells in a dose- and time-dependent manner. Flow cytometry analysis indicated that resveratrol increased cell population at sub-G1 phase, an index of apoptosis. Furthermore, resveratrol-induced cell death was associated with a collapse of the mitochondrial membrane potential. The pan-caspase inhibitor Z-VAD-fmk suppressed resveratrol-induced U251 cell death. Resveratrol stimulated autophagy was evidenced by punctuate monodansylcadaverine(MDC) staining and microtubule-associated protein light chain 3 (LC3) immunoreactivty. Resveratrol also increased protein levels of beclin 1 and membrane form LC3 (LC3-II). Autophagy inhibitors 3-methylademine (3-MA) and bafilomycin A1 sensitized the cytotoxicity of resveratrol.</p> <p>Conclusion</p> <p>Together, these findings indicate that resveratrol induces autophagy in human U251 glioma cells and autophagy suppressed resveratrol-induced apoptosis. This study thus suggests that autophagy inhibitors can increase the cytotoxicity of resveratrol to glioma cells.</p>
url http://www.biomedcentral.com/1471-2407/9/215
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