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dc.creatorJagirdar R.M., Papazoglou E.D., Pitaraki E., Kouliou O.A., Rouka E., Giannakou L., Giannopoulos S., Sinis S.I., Hatzoglou C., Gourgoulianis K.I., Zarogiannis S.G.en
dc.date.accessioned2023-01-31T08:28:45Z
dc.date.available2023-01-31T08:28:45Z
dc.date.issued2021
dc.identifier10.1111/1440-1681.13446
dc.identifier.issn03051870
dc.identifier.urihttp://hdl.handle.net/11615/74074
dc.description.abstractMalignant pleural mesothelioma (MPM) is an aggressive tumour that grows in the pleural cavity. MPM spheroids released in the pleural fluid can form new tumour foci. Cell–cell, cell–extracellular matrix (ECM) interactions in 2D and 3D impact malignant cell behaviour during cell adhesion, migration, proliferation and epithelial–mesenchymal transition (EMT). In this study, epithelioid, biphasic and sarcomatoid MPM cell types as well as benign mesothelial cells were tested with regards to the above phenotypes. Fibronectin (FN) and homologous cell-derived extracellular matrix (hcd-ECM) treated substratum differentially affected the above phenotypes. 3D MPM spheroid invasion was higher in FN-collagen matrices in the epithelioid and biphasic cells, while 3D cell cultures of epithelioid and sarcomatoid MPM cells in FN-collagen showed a higher contractility compared to hcd-ECM-collagen. Cell aggregates demonstrated invasive behaviour in hcd-ECM matrices alone. Our results suggest that ECM and the dimensionality affect malignant cell behaviour during cell culture studies. © 2020 John Wiley & Sons Australia, Ltden
dc.language.isoenen
dc.sourceClinical and Experimental Pharmacology and Physiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85097685812&doi=10.1111%2f1440-1681.13446&partnerID=40&md5=7848bd83d9d89af506c8f96eba3472d8
dc.subjectcollagenen
dc.subjectfibronectinen
dc.subjecttumor markeren
dc.subjectallogenic cellen
dc.subjectArticleen
dc.subjectcell adhesionen
dc.subjectcell aggregationen
dc.subjectcell contraction assayen
dc.subjectcell invasionen
dc.subjectcell migrationen
dc.subjectcell proliferationen
dc.subjectepithelial mesenchymal transitionen
dc.subjectepithelioid histiocyteen
dc.subjectextracellular matrixen
dc.subjecthumanen
dc.subjecthuman cellen
dc.subjectimmortalized cell lineen
dc.subjectin vitro studyen
dc.subjectmesothelium cellen
dc.subjectMeT-5A cell lineen
dc.subjectMSTO-211H cell lineen
dc.subjectphenotypeen
dc.subjectpleura mesotheliomaen
dc.subjectthree dimensional cell cultureen
dc.subjecttumor growthen
dc.subjecttumor spheroiden
dc.subjectepithelial mesenchymal transitionen
dc.subjectextracellular matrixen
dc.subjectlung tumoren
dc.subjectmesotheliomaen
dc.subjecttumor cell lineen
dc.subjectBiomarkers, Tumoren
dc.subjectCell Line, Tumoren
dc.subjectEpithelial-Mesenchymal Transitionen
dc.subjectExtracellular Matrixen
dc.subjectHumansen
dc.subjectLung Neoplasmsen
dc.subjectMesothelioma, Malignanten
dc.subjectBlackwell Publishingen
dc.titleCell and extracellular matrix interaction models in benign mesothelial and malignant pleural mesothelioma cells in 2D and 3D in-vitroen
dc.typejournalArticleen


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