<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(5)</volume><submitter>Li J</submitter><pubmed_abstract>Psoriasis is a chronic inflammatory proliferative dermatological ailment that currently lacks a definitive cure. Employing data mining techniques, this study identified a collection of substantially downregulated miRNAs (top 10). Notably, 32 targets were implicated in both the activation of the IL-17 signaling pathway and cell cycle dysregulation. &lt;i>In silico&lt;/i> analysis revealed that one of these miRNAs, miR-26a-5p, is a highly conserved cross-species miRNA. Strikingly, the miR-26a-5p sequences in humans and mice are identical, and mmu-miR-26a-5p was found to target the same 7 cell cycle targets as its human counterpart, hsa-miR-26a-5p. Among these targets, CDC6 and CCNE1 were the most effective targets of miR-26a-5p, which was further validated &lt;i>in vitro&lt;/i> using a dual luciferase r</pubmed_abstract><journal>Aging</journal><pagination>4631-4653</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10968694</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>miR-26a-5p inhibits the proliferation of psoriasis-like keratinocytes &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> by dual interference with the CDC6/CCNE1 axis.</pubmed_title><pmcid>PMC10968694</pmcid><pubmed_authors>Pang D</pubmed_authors><pubmed_authors>Zhou L</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Ouyang H</pubmed_authors><pubmed_authors>Tian Y</pubmed_authors><pubmed_authors>Yu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>miR-26a-5p inhibits the proliferation of psoriasis-like keratinocytes &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> by dual interference with the CDC6/CCNE1 axis.</name><description>Psoriasis is a chronic inflammatory proliferative dermatological ailment that currently lacks a definitive cure. Employing data mining techniques, this study identified a collection of substantially downregulated miRNAs (top 10). Notably, 32 targets were implicated in both the activation of the IL-17 signaling pathway and cell cycle dysregulation. &lt;i>In silico&lt;/i> analysis revealed that one of these miRNAs, miR-26a-5p, is a highly conserved cross-species miRNA. Strikingly, the miR-26a-5p sequences in humans and mice are identical, and mmu-miR-26a-5p was found to target the same 7 cell cycle targets as its human counterpart, hsa-miR-26a-5p. Among these targets, CDC6 and CCNE1 were the most effective targets of miR-26a-5p, which was further validated &lt;i>in vitro&lt;/i> using a dual luciferase r</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-15T20:07:04.112Z</modification><creation>2025-04-04T23:52:58.514Z</creation></dates><accession>S-EPMC10968694</accession><cross_references><pubmed>38446584</pubmed><doi>10.18632/aging.205618</doi></cross_references></HashMap>