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https://hdl.handle.net/11499/54852
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Önder, E. | - |
dc.contributor.author | Çil, N. | - |
dc.contributor.author | Seçme, M. | - |
dc.contributor.author | Mete, G.A. | - |
dc.date.accessioned | 2023-11-18T09:30:11Z | - |
dc.date.available | 2023-11-18T09:30:11Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 0378-1119 | - |
dc.identifier.uri | https://doi.org/10.1016/j.gene.2023.147880 | - |
dc.identifier.uri | https://hdl.handle.net/11499/54852 | - |
dc.description.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. | en_US |
dc.description.sponsorship | Pamukkale Üniversitesi, PAÜ: 2021TIPF006 | en_US |
dc.description.sponsorship | Notably, the Faculty of Pamukkale University Scientific Research Project Coordination Unit (grant 2021TIPF006) would be greatly acknowledged for their support. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier B.V. | en_US |
dc.relation.ispartof | Gene | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Alpha lipoic acid | en_US |
dc.subject | E-cadherin | en_US |
dc.subject | Epithelial mesenchymal transition | en_US |
dc.subject | Transforming growth factor β1 | en_US |
dc.subject | Vimentin | en_US |
dc.subject | thioctic acid | en_US |
dc.subject | transcription factor | en_US |
dc.subject | transcription factor Slug | en_US |
dc.subject | transcription factor Snail | en_US |
dc.subject | transcription factor Twist | en_US |
dc.subject | transcription factor Zeb | en_US |
dc.subject | transforming growth factor beta1 | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | uvomorulin | en_US |
dc.subject | vimentin | en_US |
dc.subject | antiproliferative activity | en_US |
dc.subject | Article | en_US |
dc.subject | cell invasion | en_US |
dc.subject | cell viability | en_US |
dc.subject | concentration (parameter) | en_US |
dc.subject | concentration response | en_US |
dc.subject | controlled study | en_US |
dc.subject | drug effect | en_US |
dc.subject | E cadherin gene | en_US |
dc.subject | epithelial mesenchymal transition | en_US |
dc.subject | female | en_US |
dc.subject | gene expression | en_US |
dc.subject | human | en_US |
dc.subject | human cell | en_US |
dc.subject | IC50 | en_US |
dc.subject | immunocytochemistry | en_US |
dc.subject | quantitative analysis | en_US |
dc.subject | real time polymerase chain reaction | en_US |
dc.subject | SK-OV-3 cell line | en_US |
dc.subject | slug gene | en_US |
dc.subject | Snail gene | en_US |
dc.subject | Twist gene | en_US |
dc.subject | vimentin gene | en_US |
dc.subject | wound healing assay | en_US |
dc.subject | Zeb gene | en_US |
dc.title | Effect of alpha lipoic acid on epithelial mesenchymal transition in SKOV-3 cells | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 892 | en_US |
dc.department | Pamukkale University | en_US |
dc.identifier.doi | 10.1016/j.gene.2023.147880 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorscopusid | 58644051800 | - |
dc.authorscopusid | 55392501500 | - |
dc.authorscopusid | 56499294100 | - |
dc.authorscopusid | 6507766696 | - |
dc.identifier.pmid | 37813206 | en_US |
dc.identifier.scopus | 2-s2.0-85174075125 | en_US |
dc.identifier.wos | WOS:001101845700001 | en_US |
dc.institutionauthor | … | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
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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