<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(8)</volume><submitter>Sarkisjan D</submitter><pubmed_abstract>(1) Background: RX-3117 (fluorocyclopentenyl-cytosine) is a cytidine analog that inhibits DNA methyltransferase 1 (DNMT1). We investigated the mechanism and potential of RX-3117 as a demethylating agent in several in vitro models. (2) Methods: we used western blotting to measure expression of several proteins known to be down-regulated by DNA methylation: O6-methylguanine-DNA methyltransferase (MGMT) and the tumor-suppressor genes, p16 and E-cadherin. Transport of methotrexate (MTX) mediated by the proton-coupled folate transporter (PCFT) was used as a functional assay. (3) Results: RX-3117 treatment decreased total DNA-cytosine-methylation in A549 non-small cell lung cancer (NSCLC) cells, and induced protein expression of MGMT, p16 and E-cadherin in A549 and SW1573 NSCLC cells. Leukemic C</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>E2717</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7215832</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>RX-3117 (Fluorocyclopentenyl-Cytosine)-Mediated Down-Regulation of DNA Methyltransferase 1 Leads to Protein Expression of Tumor-Suppressor Genes and Increased Functionality of the Proton-Coupled Folate Carrier.</pubmed_title><pmcid>PMC7215832</pmcid><pubmed_authors>Honeywell RJ</pubmed_authors><pubmed_authors>Kim DJ</pubmed_authors><pubmed_authors>Lee YB</pubmed_authors><pubmed_authors>El Hassouni B</pubmed_authors><pubmed_authors>Sarkisjan D</pubmed_authors><pubmed_authors>Kathmann I</pubmed_authors><pubmed_authors>Matherly LH</pubmed_authors><pubmed_authors>Peters GJ</pubmed_authors><pubmed_authors>Julsing JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>RX-3117 (Fluorocyclopentenyl-Cytosine)-Mediated Down-Regulation of DNA Methyltransferase 1 Leads to Protein Expression of Tumor-Suppressor Genes and Increased Functionality of the Proton-Coupled Folate Carrier.</name><description>(1) Background: RX-3117 (fluorocyclopentenyl-cytosine) is a cytidine analog that inhibits DNA methyltransferase 1 (DNMT1). We investigated the mechanism and potential of RX-3117 as a demethylating agent in several in vitro models. (2) Methods: we used western blotting to measure expression of several proteins known to be down-regulated by DNA methylation: O6-methylguanine-DNA methyltransferase (MGMT) and the tumor-suppressor genes, p16 and E-cadherin. Transport of methotrexate (MTX) mediated by the proton-coupled folate transporter (PCFT) was used as a functional assay. (3) Results: RX-3117 treatment decreased total DNA-cytosine-methylation in A549 non-small cell lung cancer (NSCLC) cells, and induced protein expression of MGMT, p16 and E-cadherin in A549 and SW1573 NSCLC cells. Leukemic C</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2025-04-05T09:49:52.055Z</modification><creation>2020-05-27T07:02:50Z</creation></dates><accession>S-EPMC7215832</accession><cross_references><pubmed>32295203</pubmed><doi>10.3390/ijms21082717</doi></cross_references></HashMap>