Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/54852
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dc.contributor.authorÖnder, E.-
dc.contributor.authorÇil, N.-
dc.contributor.authorSeçme, M.-
dc.contributor.authorMete, G.A.-
dc.date.accessioned2023-11-18T09:30:11Z-
dc.date.available2023-11-18T09:30:11Z-
dc.date.issued2024-
dc.identifier.issn0378-1119-
dc.identifier.urihttps://doi.org/10.1016/j.gene.2023.147880-
dc.identifier.urihttps://hdl.handle.net/11499/54852-
dc.description.abstractBackground: 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.sponsorshipPamukkale Üniversitesi, PAÜ: 2021TIPF006en_US
dc.description.sponsorshipNotably, the Faculty of Pamukkale University Scientific Research Project Coordination Unit (grant 2021TIPF006) would be greatly acknowledged for their support.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofGeneen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAlpha lipoic aciden_US
dc.subjectE-cadherinen_US
dc.subjectEpithelial mesenchymal transitionen_US
dc.subjectTransforming growth factor β1en_US
dc.subjectVimentinen_US
dc.subjectthioctic aciden_US
dc.subjecttranscription factoren_US
dc.subjecttranscription factor Slugen_US
dc.subjecttranscription factor Snailen_US
dc.subjecttranscription factor Twisten_US
dc.subjecttranscription factor Zeben_US
dc.subjecttransforming growth factor beta1en_US
dc.subjectunclassified drugen_US
dc.subjectuvomorulinen_US
dc.subjectvimentinen_US
dc.subjectantiproliferative activityen_US
dc.subjectArticleen_US
dc.subjectcell invasionen_US
dc.subjectcell viabilityen_US
dc.subjectconcentration (parameter)en_US
dc.subjectconcentration responseen_US
dc.subjectcontrolled studyen_US
dc.subjectdrug effecten_US
dc.subjectE cadherin geneen_US
dc.subjectepithelial mesenchymal transitionen_US
dc.subjectfemaleen_US
dc.subjectgene expressionen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectIC50en_US
dc.subjectimmunocytochemistryen_US
dc.subjectquantitative analysisen_US
dc.subjectreal time polymerase chain reactionen_US
dc.subjectSK-OV-3 cell lineen_US
dc.subjectslug geneen_US
dc.subjectSnail geneen_US
dc.subjectTwist geneen_US
dc.subjectvimentin geneen_US
dc.subjectwound healing assayen_US
dc.subjectZeb geneen_US
dc.titleEffect of alpha lipoic acid on epithelial mesenchymal transition in SKOV-3 cellsen_US
dc.typeArticleen_US
dc.identifier.volume892en_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1016/j.gene.2023.147880-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid58644051800-
dc.authorscopusid55392501500-
dc.authorscopusid56499294100-
dc.authorscopusid6507766696-
dc.identifier.pmid37813206en_US
dc.identifier.scopus2-s2.0-85174075125en_US
dc.identifier.wosWOS:001101845700001en_US
dc.institutionauthor-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. 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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