Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8928
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKüçüksayan, Hakan-
dc.contributor.authorAkça, Hakan-
dc.date.accessioned2019-08-16T12:57:11Z
dc.date.available2019-08-16T12:57:11Z
dc.date.issued2017-
dc.identifier.issn1010-4283-
dc.identifier.urihttps://hdl.handle.net/11499/8928-
dc.identifier.urihttps://doi.org/10.1177/1010428317706212-
dc.description.abstractEpithelial–mesenchymal transition is a crucial event for metastasis and could be mediated by several pathways such as phosphoinositide 3-kinase/Akt, mitogen-activated protein kinases, as well as many epigenetic regulators. Special AT-rich sequence-binding protein 2 is an epigenetic regulator involved in epithelial–mesenchymal transition and osteoblastic differentiation. It has been reported that the crosstalk between several pathways is responsible for the regulation of epithelial–mesenchymal transition in cancer cells. However, crosstalks between p38 and Akt pathways involved in epithelial–mesenchymal transition are still unknown. We recently reported that there is a crosstalk between p38 and Akt pathways in non-small-cell lung carcinoma cells, and this crosstalk is associated with E-cadherin and special AT-rich sequence-binding protein 2 expressions. Therefore, we aimed to determine whether this crosstalk has a mediator role in the regulation of epithelial–mesenchymal transition in non-small-cell lung carcinoma. Our results showed that inhibition of p38 leads to the disruption of this crosstalk via decreased expression of phosphatase and tensin homolog (PTEN) and subsequently increased activation of Akt in non-small-cell lung carcinoma cells. Then, we found that p38 inhibition upregulated special AT-rich sequence-binding protein 2 expression and reversed epithelial–mesenchymal transition in non-small-cell lung carcinoma cells. Furthermore, special AT-rich sequence-binding protein 2 knockdown abolished the effect of p38 inhibition on epithelial–mesenchymal transition in non-small-cell lung carcinoma cells. In conclusion, our results strongly indicate that the crosstalk between p38 and Akt pathways can determine special AT-rich sequence-binding protein 2 expression and epithelial character of non-small-cell lung carcinoma cells, and special AT-rich sequence-binding protein 2 is a critical epigenetic regulator for epithelial–mesenchymal transition mediated by p38 pathway in non-small-cell lung carcinoma. Our findings will contribute to illuminate the molecular mechanisms of the epithelial–mesenchymal transition process that has a critical significance for lung cancer metastasis. © 2017, © The Author(s) 2017.en_US
dc.language.isoenen_US
dc.publisherSAGE Publications Ltden_US
dc.relation.ispartofTumor Biologyen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAkten_US
dc.subjectepithelial–mesenchymal transitionen_US
dc.subjectnon-small-cell lung canceren_US
dc.subjectp38en_US
dc.subjectSATB2en_US
dc.subjectmitogen activated protein kinase p38en_US
dc.subjectphosphatidylinositol 3,4,5 trisphosphate 3 phosphataseen_US
dc.subjectprotein kinase Ben_US
dc.subjecttranscription factoren_US
dc.subjecttranscription factor SATB2en_US
dc.subjectunclassified drugen_US
dc.subjectmatrix attachment region binding proteinen_US
dc.subjectPTEN protein, humanen_US
dc.subjectSATB2 protein, humanen_US
dc.subjectAkt signalingen_US
dc.subjectArticleen_US
dc.subjectAT rich sequenceen_US
dc.subjectcontrolled studyen_US
dc.subjectenzyme activationen_US
dc.subjectepigeneticsen_US
dc.subjectepithelial mesenchymal transitionen_US
dc.subjectgene silencingen_US
dc.subjectlung metastasisen_US
dc.subjectlung non-small cell carcinoma cell lineen_US
dc.subjectmolecular dynamicsen_US
dc.subjectmolecular interactionen_US
dc.subjectnon small cell lung canceren_US
dc.subjectpriority journalen_US
dc.subjectprotein expressionen_US
dc.subjectupregulationen_US
dc.subjectbiosynthesisen_US
dc.subjectgene expression regulationen_US
dc.subjecthumanen_US
dc.subjectlung tumoren_US
dc.subjectMAPK signalingen_US
dc.subjectmetabolismen_US
dc.subjectpathologyen_US
dc.subjectphysiologyen_US
dc.subjectsignal transductionen_US
dc.subjecttumor cell lineen_US
dc.subjectWestern blottingen_US
dc.subjectBlotting, Westernen_US
dc.subjectCarcinoma, Non-Small-Cell Lungen_US
dc.subjectCell Line, Tumoren_US
dc.subjectEpithelial-Mesenchymal Transitionen_US
dc.subjectGene Expression Regulation, Neoplasticen_US
dc.subjectGene Knockdown Techniquesen_US
dc.subjectHumansen_US
dc.subjectLung Neoplasmsen_US
dc.subjectMAP Kinase Signaling Systemen_US
dc.subjectMatrix Attachment Region Binding Proteinsen_US
dc.subjectProto-Oncogene Proteins c-akten_US
dc.subjectPTEN Phosphohydrolaseen_US
dc.subjectReceptor Cross-Talken_US
dc.subjectSignal Transductionen_US
dc.subjectTranscription Factorsen_US
dc.titleThe crosstalk between p38 and Akt signaling pathways orchestrates EMT by regulating SATB2 expression in NSCLC cellsen_US
dc.typeArticleen_US
dc.identifier.volume39en_US
dc.identifier.issue9en_US
dc.identifier.doi10.1177/1010428317706212-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85031408155en_US
dc.identifier.wosWOS:000383616901419en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairetypeArticle-
crisitem.author.dept14.02. Internal Medicine-
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
Files in This Item:
File SizeFormat 
crosstalk.pdf556.73 kBAdobe PDFView/Open
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

17
checked on Sep 1, 2024

Page view(s)

40
checked on Aug 24, 2024

Download(s)

12
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.