<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fahim SA</submitter><funding>Academy of Scientific Research and Technology</funding><pagination>125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11764005</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(2)</volume><pubmed_abstract>Meis1 is a transcription factor involved in numerous functions including development and proliferation and has been previously shown to harness cell cycle progression. In this study, we used in silico analysis to predict that miR-499-5p targets Meis1 and that Malat1 sponges miR-499-5p. For the first time, we demonstrated that the overexpression of miR-499-5p led to the downregulation of Meis1 mRNA and protein in C166 cells by directly binding to its 3'UTR. Moreover, knocking down Malat1 increased miR-499-5p expression, subsequently suppressing Meis1. Through BrdU incorporation assay, we showed that the knockdown of Malat1, Meis1, or mimicking with miR-499-5p promoted cell proliferation. Enrichment analyses on proteins identified via mass spectrometry after manipulating Malat1, miR-499-5p, </pubmed_abstract><journal>Cells</journal><pubmed_title>Interaction Between Malat1 and miR-499-5p Regulates Meis1 Expression and Function with a Net Impact on Cell Proliferation.</pubmed_title><pmcid>PMC11764005</pmcid><funding_grant_id>ASRT-JESOR 3113</funding_grant_id><pubmed_authors>Osama A</pubmed_authors><pubmed_authors>Abdellatif A</pubmed_authors><pubmed_authors>Fayed IH</pubmed_authors><pubmed_authors>Karam A</pubmed_authors><pubmed_authors>Fawzy IO</pubmed_authors><pubmed_authors>Metwale R</pubmed_authors><pubmed_authors>El Sobky SA</pubmed_authors><pubmed_authors>Magdeldin S</pubmed_authors><pubmed_authors>Elsayed MDAA</pubmed_authors><pubmed_authors>El-Ekiaby N</pubmed_authors><pubmed_authors>Ragheb M</pubmed_authors><pubmed_authors>Abdelaziz AI</pubmed_authors><pubmed_authors>Fahim SA</pubmed_authors><pubmed_authors>Sadek HA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interaction Between Malat1 and miR-499-5p Regulates Meis1 Expression and Function with a Net Impact on Cell Proliferation.</name><description>Meis1 is a transcription factor involved in numerous functions including development and proliferation and has been previously shown to harness cell cycle progression. In this study, we used in silico analysis to predict that miR-499-5p targets Meis1 and that Malat1 sponges miR-499-5p. For the first time, we demonstrated that the overexpression of miR-499-5p led to the downregulation of Meis1 mRNA and protein in C166 cells by directly binding to its 3'UTR. Moreover, knocking down Malat1 increased miR-499-5p expression, subsequently suppressing Meis1. Through BrdU incorporation assay, we showed that the knockdown of Malat1, Meis1, or mimicking with miR-499-5p promoted cell proliferation. Enrichment analyses on proteins identified via mass spectrometry after manipulating Malat1, miR-499-5p, </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-04-15T03:20:49.563Z</modification><creation>2025-04-05T19:21:02.898Z</creation></dates><accession>S-EPMC11764005</accession><cross_references><pubmed>39851553</pubmed><doi>10.3390/cells14020125</doi></cross_references></HashMap>