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題名 Valproic acid inhibits glioblastoma multiforme cell growth via paraoxonase 2 expression.
作者 蕭勝煌
Tseng, Jen-Ho
Chen, Cheng-Yi
Chen, Pei-Chun
Hsiao, Sheng-Huang
Fan, Chi-Chen
Liang, Yu-Chih
Chen, Chie-Pein
貢獻者 心理系
日期 2017-02
上傳時間 15-Jan-2018 11:39:39 (UTC+8)
摘要 We studied the potential mechanisms of valproic acid (VPA) in the treatment of glioblastoma multiforme (GBM). Using the human U87, GBM8401, and DBTRG-05MG GBM-derived cell lines, VPA at concentrations of 5 to 20 mM induced G2/M cell cycle arrest and increased the production of reactive oxygen species (ROS). Stress-related molecules such as paraoxonase 2 (PON2), cyclin B1, cdc2, and Bcl-xL were downregulated, but p27, p21 and Bim were upregulated by VPA treatment. VPA response element on the PON2 promoter was localized at position -400/-1. PON2 protein expression was increased in GBM cells compared with normal brain tissue and there was a negative correlation between the expression of PON2 and Bim. These findings were confirmed by the public Bredel GBM microarray (Gene Expression Omnibus accession: GSE2223) and the Cancer Genome Atlas GBM microarray datasets. Overexpression of PON2 in GBM cells significantly decreased intracellular ROS levels, and PON2 expression was decreased after VPA stimulation compared with controls. Bim expression was significantly induced by VPA in GBM cells with PON2 silencing. These observations were further shown in the subcutaneous GBM8401 cell xenograft of BALB/c nude mice. Our results suggest that VPA reduces PON2 expression in GBM cells, which in turn increases ROS production and induces Bim production that inhibits cancer progression via the PON2-Bim cascade.
關聯 Oncotarget , 2017; 8:14666-14679
資料類型 article
DOI http://dx.doi.org/10.18632/oncotarget.14716
dc.contributor 心理系zh_TW
dc.creator (作者) 蕭勝煌zh_TW
dc.creator (作者) Tseng, Jen-Hoen_US
dc.creator (作者) Chen, Cheng-Yien_US
dc.creator (作者) Chen, Pei-Chunen_US
dc.creator (作者) Hsiao, Sheng-Huangen_US
dc.creator (作者) Fan, Chi-Chenen_US
dc.creator (作者) Liang, Yu-Chihen_US
dc.creator (作者) Chen, Chie-Peinen_US
dc.date (日期) 2017-02
dc.date.accessioned 15-Jan-2018 11:39:39 (UTC+8)-
dc.date.available 15-Jan-2018 11:39:39 (UTC+8)-
dc.date.issued (上傳時間) 15-Jan-2018 11:39:39 (UTC+8)-
dc.identifier.uri (URI) http://nccur.lib.nccu.edu.tw/handle/140.119/115566-
dc.description.abstract (摘要) We studied the potential mechanisms of valproic acid (VPA) in the treatment of glioblastoma multiforme (GBM). Using the human U87, GBM8401, and DBTRG-05MG GBM-derived cell lines, VPA at concentrations of 5 to 20 mM induced G2/M cell cycle arrest and increased the production of reactive oxygen species (ROS). Stress-related molecules such as paraoxonase 2 (PON2), cyclin B1, cdc2, and Bcl-xL were downregulated, but p27, p21 and Bim were upregulated by VPA treatment. VPA response element on the PON2 promoter was localized at position -400/-1. PON2 protein expression was increased in GBM cells compared with normal brain tissue and there was a negative correlation between the expression of PON2 and Bim. These findings were confirmed by the public Bredel GBM microarray (Gene Expression Omnibus accession: GSE2223) and the Cancer Genome Atlas GBM microarray datasets. Overexpression of PON2 in GBM cells significantly decreased intracellular ROS levels, and PON2 expression was decreased after VPA stimulation compared with controls. Bim expression was significantly induced by VPA in GBM cells with PON2 silencing. These observations were further shown in the subcutaneous GBM8401 cell xenograft of BALB/c nude mice. Our results suggest that VPA reduces PON2 expression in GBM cells, which in turn increases ROS production and induces Bim production that inhibits cancer progression via the PON2-Bim cascade.en_US
dc.format.extent 3592907 bytes-
dc.format.mimetype application/pdf-
dc.relation (關聯) Oncotarget , 2017; 8:14666-14679en_US
dc.title (題名) Valproic acid inhibits glioblastoma multiforme cell growth via paraoxonase 2 expression.en_US
dc.type (資料類型) article
dc.identifier.doi (DOI) 10.18632/oncotarget.14716
dc.doi.uri (DOI) http://dx.doi.org/10.18632/oncotarget.14716