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dc.contributor.authorTrepiana Arin, Jenifer ORCID
dc.contributor.authorMeijide de la Fuente, Susana
dc.contributor.authorNavarro Lobato, Rosaura
dc.contributor.authorHernández, María Luisa
dc.contributor.authorRuiz Sanz, José Ignacio
dc.contributor.authorRuiz Larrea, María Begoña ORCID
dc.date.accessioned2018-06-18T07:59:21Z
dc.date.available2018-06-18T07:59:21Z
dc.date.issued2017-08
dc.identifier.citationRedox Biology 12 : 103-113 (2017)es_ES
dc.identifier.issn2213-2317
dc.identifier.urihttp://hdl.handle.net/10810/27567
dc.description.abstractMost of the in vitro studies using liver cell lines have been performed under atmospheric oxygen partial pressure (21% O-2). However, the oxygen concentrations in the liver and cancer cells are far from this value. In the present study, we have evaluated the influence of oxygen on 1) the tumor cell lines features (growth, steadystate ROS levels, GSH content, activities of antioxidant enzymes, p66 Shc and SOD expressions, metalloproteinases secretion, migration, invasion, and adhesion) of human hepatocellular carcinoma cell lines, and b) the response of the cells to an oxidant stimulus (aqueous leaf extract of the V. baccifera plant species). For this purpose, three hepatocarcinoma cell lines with different p53 status, HepG2 (wild-type), Huh7 (mutated), and Hep3B (deleted), were cultured (6-30 days) under atmospheric (21%) and more physiological (8%) pO(2). Results showed that after long-term culturing at 8% versus 21% O-2, the cellular proliferation rate and the steady-state levels of mitochondrial O-2-were unaffected. However, the intracellular basal ROS levels were higher independently of the characteristics of the cell line. Moreover, the lower pO(2) was associated with lower glutathione content, the induction of p66 Shc and Mn-SOD proteins, and increased SOD activity only in HepG2. This cell line also showed a higher migration rate, secretion of active metalloproteinases, and a faster invasion. HepG2 cells were more resistant to the oxidative stress induced by V. baccifera. Results suggest that the longterm culturing of human hepatoma cells at a low, more physiological pO(2) induces antioxidant adaptations that could be mediated by p53, and may alter the cellular response to a subsequent oxidant challenge. Data support the necessity of validating outcomes from studies performed with hepatoma cell cultures under ambient O-2.es_ES
dc.description.sponsorshipThis work was supported by research grants from the Basque Government (Department of Education, Universities and Research, ref. IT687-13), and University of the Basque Country, UPV/EHU (CLUMBER UFI11/20 and pre-doctoral and post-doctoral grants to J.T.). We thank Jose Antonio Lopez for his valuable technical assistance with cell cultures. Technical and human support provided by SGIKer (UPV/EHU, MICINN, GV/EJ, ESF) is gratefully acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherElsevier Science BVes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectoxygen tensiones_ES
dc.subjecthepatoma cellses_ES
dc.subjectsuperoxide dismutasees_ES
dc.subjectcell migrationes_ES
dc.titleInfluence Of Oxygen Partial Pressure On The Characteristics Of Human Hepatocarcinoma Cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/)es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/search?pub=Redox%20Biology&volume=12&page=103-113&show=25&sortBy=relevance&origin=jrnl_home&zone=search&cid=282796es_ES
dc.identifier.doi10.1016/j.redox.2017.02.004
dc.departamentoesFisiologíaes_ES
dc.departamentoeuFisiologiaes_ES


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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/)
Except where otherwise noted, this item's license is described as This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/)