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dc.contributor.authorAsweto, Collins O.
dc.contributor.authorWu, J.
dc.contributor.authorAlzain, M. A.
dc.contributor.authorHu, H.
dc.contributor.authorAndrea, S.
dc.contributor.authorFeng, L.
dc.contributor.authorYeng, X.
dc.contributor.authorDuan, J.
dc.contributor.authorSun, Z.
dc.date.accessioned2018-10-11T17:08:11Z
dc.date.available2018-10-11T17:08:11Z
dc.date.issued2017-12
dc.identifier.citationEnviron Toxicol Pharmacol. 2017 Dec;56:191-197en_US
dc.identifier.urioi: 10.1016/j.etap.2017.09.012. Epub 2017 Sep 20
dc.identifier.urihttp://hdl.handle.net/123456789/2081
dc.description.abstractSilica nanoparticles (SiNPs) have been found to pass through biological barriers and get distributed in the human body. They induce cell apoptosis via various mechanisms in body organs. To understand these mechanisms, we carried out systematic review of in vitro studies on SiNPs-induced cell apoptosis. Office of Health Assessment and Translation approach for Systematic Review and Evidence Integration was used to identify 14 studies dating from the year 2000 to current. Four studies showed an increase in DNA damage, cell cycle arrest, proapoptotic factors and decrease in antiapoptotic factors resulting to apoptosis. Eight studies showed induction of mitochondrial dysfunction, Bax upregulation, Bcl-2 downregulation, and caspase-3, -7, -9 activities increase. Increase in FADD, TNFR1 and Bid proteins was observed in one study, while the other NO production and caspase-3 activity was increased. These studies found the potency of SiNPs to induce cell apoptosis through DNA damage, mitochondrial, tumor necrosis factor, and nitric oxide related pathways.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectCell apoptosisen_US
dc.subjectDNA damageen_US
dc.subjectIn vitro studiesen_US
dc.subjectMitochodrial damageen_US
dc.subjectPathwaysen_US
dc.subjectSilica nanoparticlesen_US
dc.titleCellular pathways involved in silica nanoparticles induced apoptosis: A systematic review of in vitro studies.en_US
dc.typeArticleen_US


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