<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>46(2)</volume><submitter>Fallahzadeh-Abarghooei L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Sodium arsenite (NaAsO2) has potent cytotoxic activity in human cancer cells. Oxidative stress has been suggested as a mechanism for arsenic-induced carcinogenesis. The purpose of the present study was to evaluate the alteration of mRNA levels of catalase (&lt;i>CAT&lt;/i>) and superoxide dismutase 2 (&lt;i>SOD2&lt;/i>) in MCF-7 and Jurkat cells after exposure to NaAsO&lt;sub>2&lt;/sub>.&lt;h4>Methods&lt;/h4>Methylthiazol tetrazolium (MTT) viability assay was performed to evaluate cytotoxicity of NaAsO&lt;sub>2&lt;/sub> in MCF-7 and Jurkat cells. For evaluating the expression levels of the &lt;i>CAT&lt;/i> and &lt;i>SOD2&lt;/i>, we used two concentrations of NaAsO&lt;sub>2&lt;/sub> (5 and 15 μM), lower than the concentrations at which 50% of cell viability were lost. The cells were treated with co-treatment of NaAsO&lt;s</pubmed_abstract><journal>Iranian journal of public health</journal><pagination>229-234</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5402782</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effect of Sodium Arsenite on the Expression of Antioxidant Genes (&lt;i>SOD2&lt;/i> and &lt;i>CAT&lt;/i>) in MCF-7 and Jurkat Cell Lines.</pubmed_title><pmcid>PMC5402782</pmcid><pubmed_authors>Fallahzadeh-Abarghooei L</pubmed_authors><pubmed_authors>Saadat M</pubmed_authors><pubmed_authors>Samadaei-Ghadikolaie M</pubmed_authors><pubmed_authors>Saadat I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of Sodium Arsenite on the Expression of Antioxidant Genes (&lt;i>SOD2&lt;/i> and &lt;i>CAT&lt;/i>) in MCF-7 and Jurkat Cell Lines.</name><description>&lt;h4>Background&lt;/h4>Sodium arsenite (NaAsO2) has potent cytotoxic activity in human cancer cells. Oxidative stress has been suggested as a mechanism for arsenic-induced carcinogenesis. The purpose of the present study was to evaluate the alteration of mRNA levels of catalase (&lt;i>CAT&lt;/i>) and superoxide dismutase 2 (&lt;i>SOD2&lt;/i>) in MCF-7 and Jurkat cells after exposure to NaAsO&lt;sub>2&lt;/sub>.&lt;h4>Methods&lt;/h4>Methylthiazol tetrazolium (MTT) viability assay was performed to evaluate cytotoxicity of NaAsO&lt;sub>2&lt;/sub> in MCF-7 and Jurkat cells. For evaluating the expression levels of the &lt;i>CAT&lt;/i> and &lt;i>SOD2&lt;/i>, we used two concentrations of NaAsO&lt;sub>2&lt;/sub> (5 and 15 μM), lower than the concentrations at which 50% of cell viability were lost. The cells were treated with co-treatment of NaAsO&lt;s</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Feb</publication><modification>2025-04-05T12:54:45.371Z</modification><creation>2019-06-06T17:21:57Z</creation></dates><accession>S-EPMC5402782</accession><cross_references><pubmed>28451559</pubmed></cross_references></HashMap>