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https://hdl.handle.net/11499/8099
Title: | Tumour suppressor PTEN enhanced enzyme activity of GPx, SOD and catalase by suppression of PI3K/AKT pathway in non-small cell lung cancer cell lines | Authors: | Akça, Hakan Demiray, Aydın Aslan, M. Açıkbaş, İbrahim Tokgun, Onur |
Keywords: | Catalase GPx NSCLC PTEN SOD catalase glutathione peroxidase phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase protein kinase B superoxide dismutase phosphatidate phosphatase phosphatidylinositol 3 kinase antibody labeling article enzyme activity enzyme repression gene deletion genetic transfection human human cell lung non small cell cancer priority journal protein expression stable expression transient expression tumor suppressor gene upregulation Western blotting Article cancer cell line controlled study enzyme inhibition lung alveolus cell non small cell lung cancer oxidative stress protein domain signal transduction Carcinoma, Non-Small-Cell Lung Cell Line, Tumor Gene Expression Regulation, Neoplastic Glutathione Peroxidase Humans Lung Neoplasms Oxidative Stress Phosphatidylinositol 3-Kinases Proto-Oncogene Proteins c-akt PTEN Phosphohydrolase |
Abstract: | Phosphates and tensin homologue deleted on chromosome 10 (PTEN) is a tumour suppressor gene which dephosphorilates phosphoinositol 3,4,5 triphosphates. Therefore PTEN can regulate PI3K/AKT pathway in cells. Because of promoter methylation or gene deletion, PTEN expression is commonly decreased or lost in non-small cell lung cancer (NSCLC) cell lines. Therefore, we hypothesized that PTEN could regulate the activity of superoxide dismutase (CuZnSOD), glutathione peroxidase (GPx) and catalase. We first recreated PTENwt, G129R and G129E expressions in lung cell lines, in which endogenous PTEN expression was not detected. Then, we showed that PTEN could suppress AKT activity by its lipid phosphatase domain. We then examined the effect of recreated PTEN expressions in NSCLC cells. While PTENwt expression caused enhanced activity of SOD, GPx and catalase in transfected cells lines, neither G129R nor G129E expression effected enzyme activities. These results suggest that PTEN can up-regulate SOD, GPx and catalase activity by inhibition of PI3K/AKT pathway in NSCLC cell lines. © 2013 Informa UK, Ltd. | URI: | https://hdl.handle.net/11499/8099 https://doi.org/10.3109/14756366.2011.654114 |
ISSN: | 1475-6366 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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10.3109 14756366.2011.654114.pdf | 963.77 kB | Adobe PDF | View/Open |
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