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dc.creatorSinis S.I., Hatzoglou C., Gourgoulianis K.I., Zarogiannis S.G.en
dc.date.accessioned2023-01-31T09:56:38Z
dc.date.available2023-01-31T09:56:38Z
dc.date.issued2018
dc.identifier10.3389/fphys.2018.00295
dc.identifier.issn1664042X
dc.identifier.urihttp://hdl.handle.net/11615/79017
dc.description.abstractNanoparticles have great potential for numerous applications due to their unique physicochemical properties. However, concerns have been raised that they may induce deleterious effects on biological systems. There is accumulating evidence that, like asbestos, inhaled nanomaterials of >5 μm and high aspect ratio (3:1), particularly rod-like carbon nanotubes, may inflict pleural disease including mesothelioma. Additionally, a recent set of case reports suggests that inhalation of polyacrylate/nanosilica could in part be associated with inflammation and fibrosis of the pleura of factory workers. However, the adverse outcomes of nanoparticle exposure to mesothelial tissues are still largely unexplored. In that context, the present review aims to provide an overview of the relevant pathophysiological implications involving toxicological studies describing effects of engineered nanoparticles on mesothelial cells and membranes. In vitro studies primarily emphasize on simulating cellular uptake and toxicity of nanotubes on benign or malignant cell lines. On the other hand, in vivo studies focus on illustrating endpoints of serosal pathology in rodent animal models. From a molecular aspect, some nanoparticle categories are shown to be cytotoxic and genotoxic after acute treatment, whereas chronic incubation may lead to malignant-like transformation. At an organism level, a number of fibrous shaped nanotubes are related with features of chronic inflammation and MWCNT-7 is the only type to consistently inflict mesothelioma. © 2018 Sinis, Hatzoglou, Gourgoulianis and Zarogiannis.en
dc.language.isoenen
dc.sourceFrontiers in Physiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85044870667&doi=10.3389%2ffphys.2018.00295&partnerID=40&md5=d13da40d4f005d81b183700b513b6fc3
dc.subjectcarbon nanotubeen
dc.subjectmulti walled nanotubeen
dc.subjectnanomaterialen
dc.subjectnanoparticleen
dc.subjectnickelen
dc.subjectnickel nanoparticleen
dc.subjectpolyacrylic aciden
dc.subjectsilica nanoparticleen
dc.subjectsingle walled nanotubeen
dc.subjectcarcinogenicityen
dc.subjectchronic inflammationen
dc.subjectcytotoxicityen
dc.subjectDNA damageen
dc.subjectgenotoxicityen
dc.subjecthumanen
dc.subjectmembrane permeabilityen
dc.subjectmesothelium cellen
dc.subjectmyeloid-derived suppressor cellen
dc.subjectnanotoxicologyen
dc.subjectnonhumanen
dc.subjectparticle sizeen
dc.subjectpathophysiologyen
dc.subjectphysical chemistryen
dc.subjectpleura diseaseen
dc.subjectpleura mesotheliomaen
dc.subjectpleural fibrosisen
dc.subjectpleurisyen
dc.subjectReviewen
dc.subjectstructure activity relationen
dc.subjectFrontiers Media S.A.en
dc.titleCarbon nanotubes and other engineered nanoparticles induced pathophysiology on mesothelial cells and mesothelial membranesen
dc.typeotheren


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