Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/54852
Title: Effect of alpha lipoic acid on epithelial mesenchymal transition in SKOV-3 cells
Authors: Önder, E.
Çil, N.
Seçme, M.
Mete, G.A.
Keywords: Alpha lipoic acid
E-cadherin
Epithelial mesenchymal transition
Transforming growth factor β1
Vimentin
thioctic acid
transcription factor
transcription factor Slug
transcription factor Snail
transcription factor Twist
transcription factor Zeb
transforming growth factor beta1
unclassified drug
uvomorulin
vimentin
antiproliferative activity
Article
cell invasion
cell viability
concentration (parameter)
concentration response
controlled study
drug effect
E cadherin gene
epithelial mesenchymal transition
female
gene expression
human
human cell
IC50
immunocytochemistry
quantitative analysis
real time polymerase chain reaction
SK-OV-3 cell line
slug gene
Snail gene
Twist gene
vimentin gene
wound healing assay
Zeb gene
Publisher: Elsevier B.V.
Abstract: Background: Ovarian cancer is the fifth leading cause of cancer-related death in women. Patients are usually diagnosed with advanced tumor metastass. Epithelial over cancer cells spread from primary tumor by undergoing epithelial mesenchymal transition (EMT). It has been suggested that alpha lipoic acid (ALA), a natural antioxidant lipophilic compound, reduces the oxidative stress by causing apoptosis and inhibition of proliferation of cell in cancer cells. The aim of our study was to establish a transforming growth factor β1 (TGF β1) dependent epithelial mesenchymal transition model in the SKOV-3 ovarian adenocarcinoma cell line which is an epithelial subtype of ovarian cancer and to investigate the effects of alpha lipoic acid on EMT and ovarian cancer migration. Methods: For establish an EMT model, SKOV-3 cells were treated with different dose of TGF β1 and XTT cell viability kit was used to find IC 50 dose of ALA. Four different groups that are control, TGF β1, ALA and ALA + TGF β1 were created. Changes in the expression of genes related to EMT markers that are E-cadherin, vimentin, Snail, Slug, Twist and Zeb were analyzed with quantitative real-time PCR. These proteins were determined with the immunocytochemistry method. The migration capacity was analyzed with wound healing assay. Matrigel invasion capacity test was used to show invasion and colonization test to show colonization. Results: The dose of TGF β1 was determined 100 ng/ml at 72 h, the IC50 dose of ALA 219.033 µM at 48 h was determined. EMT markers in the TGF β1 group were compatible with EMT and it was shown to inhibit EMT in the groups given ALA. According to wound healing, colonization and invasion experiments, proliferation and invasion increased in TGF β1 group, but decreased in ALA and combined groups (p < 0.05). Conclusion: These results indicate that ALA suppresses the metastasis of ovarian cancer cells by regulating EMT, implying that ALA might be a potential therapeutic agent for the treatment of ovarian cancer. © 2023 Elsevier B.V.
URI: https://doi.org/10.1016/j.gene.2023.147880
https://hdl.handle.net/11499/54852
ISSN: 0378-1119
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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