Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma

<p>Abstract</p> <p>Background</p> <p>Statins are inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis. The inhibition of this key enzyme in the mevalonate pathway leads to suppression of cell proliferation and...

Full description

Bibliographic Details
Main Authors: Itoh Tatsuki, Satou Takao, Tsubaki Masanobu, Yanae Masashi, Imano Motohiro, Yamazoe Yuzuru, Nishida Shozo
Format: Article
Language:English
Published: BMC 2011-08-01
Series:Journal of Experimental & Clinical Cancer Research
Subjects:
ERK
Akt
Online Access:http://www.jeccr.com/content/30/1/74
id doaj-e7059f8af7224565a30e3166a298913f
record_format Article
spelling doaj-e7059f8af7224565a30e3166a298913f2020-11-25T01:41:58ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662011-08-013017410.1186/1756-9966-30-74Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastomaItoh TatsukiSatou TakaoTsubaki MasanobuYanae MasashiImano MotohiroYamazoe YuzuruNishida Shozo<p>Abstract</p> <p>Background</p> <p>Statins are inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis. The inhibition of this key enzyme in the mevalonate pathway leads to suppression of cell proliferation and induction of apoptosis. However, the molecular mechanism of apoptosis induction by statins is not well understood in glioblastoma. In the present study, we attempted to elucidate the mechanism by which statins induce apoptosis in C6 glioma cells.</p> <p>Methods</p> <p>The cytotoxicity of statins toward the C6 glioma cells were evaluated using a cell viability assay. The enzyme activity of caspase-3 was determined using activity assay kits. The effects of statins on signal transduction molecules were determined by western blot analyses.</p> <p>Results</p> <p>We found that statins inhibited cell proliferation and induced apoptosis in these cells. We also observed an increase in caspase-3 activity. The apoptosis induced by statins was not inhibited by the addition of farnesyl pyrophosphate, squalene, ubiquinone, and isopentenyladenine, but by geranylgeranyl-pyrophosphate (GGPP). Furthermore, statins decreased the levels of phosphorylated extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt.</p> <p>Conclusions</p> <p>These results suggest that statins induce apoptosis when GGPP biosynthesis is inhibited and consequently decreases the level of phosphorylated ERK1/2 and Akt. The results of this study also indicate that statins could be used as anticancer agents in glioblastoma.</p> http://www.jeccr.com/content/30/1/74statinsC6 gliomaERKAkt
collection DOAJ
language English
format Article
sources DOAJ
author Itoh Tatsuki
Satou Takao
Tsubaki Masanobu
Yanae Masashi
Imano Motohiro
Yamazoe Yuzuru
Nishida Shozo
spellingShingle Itoh Tatsuki
Satou Takao
Tsubaki Masanobu
Yanae Masashi
Imano Motohiro
Yamazoe Yuzuru
Nishida Shozo
Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
Journal of Experimental & Clinical Cancer Research
statins
C6 glioma
ERK
Akt
author_facet Itoh Tatsuki
Satou Takao
Tsubaki Masanobu
Yanae Masashi
Imano Motohiro
Yamazoe Yuzuru
Nishida Shozo
author_sort Itoh Tatsuki
title Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
title_short Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
title_full Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
title_fullStr Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
title_full_unstemmed Statin-induced apoptosis via the suppression of ERK1/2 and Akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
title_sort statin-induced apoptosis via the suppression of erk1/2 and akt activation by inhibition of the geranylgeranyl-pyrophosphate biosynthesis in glioblastoma
publisher BMC
series Journal of Experimental & Clinical Cancer Research
issn 1756-9966
publishDate 2011-08-01
description <p>Abstract</p> <p>Background</p> <p>Statins are inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis. The inhibition of this key enzyme in the mevalonate pathway leads to suppression of cell proliferation and induction of apoptosis. However, the molecular mechanism of apoptosis induction by statins is not well understood in glioblastoma. In the present study, we attempted to elucidate the mechanism by which statins induce apoptosis in C6 glioma cells.</p> <p>Methods</p> <p>The cytotoxicity of statins toward the C6 glioma cells were evaluated using a cell viability assay. The enzyme activity of caspase-3 was determined using activity assay kits. The effects of statins on signal transduction molecules were determined by western blot analyses.</p> <p>Results</p> <p>We found that statins inhibited cell proliferation and induced apoptosis in these cells. We also observed an increase in caspase-3 activity. The apoptosis induced by statins was not inhibited by the addition of farnesyl pyrophosphate, squalene, ubiquinone, and isopentenyladenine, but by geranylgeranyl-pyrophosphate (GGPP). Furthermore, statins decreased the levels of phosphorylated extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt.</p> <p>Conclusions</p> <p>These results suggest that statins induce apoptosis when GGPP biosynthesis is inhibited and consequently decreases the level of phosphorylated ERK1/2 and Akt. The results of this study also indicate that statins could be used as anticancer agents in glioblastoma.</p>
topic statins
C6 glioma
ERK
Akt
url http://www.jeccr.com/content/30/1/74
work_keys_str_mv AT itohtatsuki statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
AT satoutakao statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
AT tsubakimasanobu statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
AT yanaemasashi statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
AT imanomotohiro statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
AT yamazoeyuzuru statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
AT nishidashozo statininducedapoptosisviathesuppressionoferk12andaktactivationbyinhibitionofthegeranylgeranylpyrophosphatebiosynthesisinglioblastoma
_version_ 1725038523535327232