Please use this identifier to cite or link to this item: 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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