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dc.date.accessioned2023-09-06T16:14:00Z
dc.date.available2023-09-06T16:14:00Z
dc.date.created2023-09-01T13:45:33Z
dc.date.issued2023
dc.identifier.citationSharma, Sunita Khan, Qalbi Schreurs, Olaf Joseph Franciscus Sapkota, Dipak Samuelsen, Jan Tore . Investigation of biological effects of HEMA in 3D-organotypic co-culture models of normal and malignant oral keratinocytes. Biomaterial Investigations in Dentistry. 2023
dc.identifier.urihttp://hdl.handle.net/10852/104488
dc.description.abstractSeveral in vitro studies utilizing 2-dimensional (2D) cell culture systems have linked 2-hydroxyethyl methacrylate (HEMA) with cytotoxic effects in oral mucosa and dental pulp cells. Although such studies are invaluable in dissecting the cellular and molecular effects of HEMA, there is a growing interest in the utilization of appropriate 3-dimensional (3D) models that mimic the structure of oral mucosa. Using a previously characterized 3D-organotypic co-culture model, this study aimed to investigate the cellular and molecular effects of HEMA on a 3D-co-culture model consisting of primary normal oral keratinocyte (NOK) grown directly on top of collagen I gel containing primary oral fibroblasts (NOF). The second aim was to examine the suitability of a 3D-co-culture system consisting of oral squamous cell carcinoma (OSCC) cells as a model system to investigate the biological effects of HEMA. We demonstrated that HEMA treatment led to reduced viability of NOK, NOF and OSCC-cell lines in 2D-culture. The keratinocytes in 3D-co-cultures of NOK and OSCC-cells reacted similarly with respect to cell proliferation and activation of autophagy flux, to HEMA treatment. Nevertheless, NOK was found to be more susceptible to apoptosis following HEMA treatment than OSCC in 3D-co-cultures. These results indicate that 3D-organotypic co-cultures of NOK might represent an appropriate model system for the investigation of the biological effects of HEMA and other dental biomaterials. Given the challenges in obtaining primary cultures of NOK and issues associated with their rapid differentiation in culture, the possible use of OSCC cells as an alternative to NOK for 3D models represents an area for future research.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleInvestigation of biological effects of HEMA in 3D-organotypic co-culture models of normal and malignant oral keratinocytes
dc.title.alternativeENEngelskEnglishInvestigation of biological effects of HEMA in 3D-organotypic co-culture models of normal and malignant oral keratinocytes
dc.typeJournal article
dc.creator.authorSharma, Sunita
dc.creator.authorKhan, Qalbi
dc.creator.authorSchreurs, Olaf Joseph Franciscus
dc.creator.authorSapkota, Dipak
dc.creator.authorSamuelsen, Jan Tore
cristin.unitcode185,16,15,0
cristin.unitnameInstitutt for oral biologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2171690
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomaterial Investigations in Dentistry&rft.volume=&rft.spage=&rft.date=2023
dc.identifier.jtitleBiomaterial Investigations in Dentistry
dc.identifier.doihttps://doi.org/10.1080/26415275.2023.2234400
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2641-5275
dc.type.versionPublishedVersion
cristin.articleid2234400


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