<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(2)</volume><submitter>Liu Y</submitter><funding>Doctoral Scientific Research Foundation of Liaoning Province</funding><pubmed_abstract>This study investigated the function of long non-coding RNA (lncRNA) cytoskeleton regulator RNA (CYTOR) in hepatocellular carcinoma (HCC). In HCC, the expression of CYTOR and microRNA (miR)-125a-5p were measured by quantitative real-time PCR (qRT-PCR). The expression of actin skeletal protein 1 (LASP1) was evaluated by Western blot analysis. Flow cytometry assays, transwell assays, colony formation assay, and cell counting kit-8 (CCK-8) assay were used to evaluate the roles of miR-125a-5p and CYTOR in HCC cells. The target genes of CYTOR and miR-125a-5p were identified by bioinformatics analysis and Luciferase assay. CYTOR was upregulated in HCC cell lines, and knockdown of CYTOR inhibited HCC cell growth. MiR-125a-5p was downregulated in HCC cells and a target of CYTOR in regulating HCC progression. Furthermore, LASP1 was a downstream target of miR-125a-5p. Finally, CYTOR was found to be involved in HCC progression &lt;i>in vivo&lt;/i>. CYTOR promotes HCC development by regulating the miR-125a-5p/LASP1 axis.</pubmed_abstract><journal>Bioengineered</journal><pagination>3666-3679</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8974008</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Long non-coding RNA (lncRNA) CYTOR promotes hepatocellular carcinoma proliferation by targeting the microRNA-125a-5p/LASP1 axis.</pubmed_title><pmcid>PMC8974008</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Geng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long non-coding RNA (lncRNA) CYTOR promotes hepatocellular carcinoma proliferation by targeting the microRNA-125a-5p/LASP1 axis.</name><description>This study investigated the function of long non-coding RNA (lncRNA) cytoskeleton regulator RNA (CYTOR) in hepatocellular carcinoma (HCC). In HCC, the expression of CYTOR and microRNA (miR)-125a-5p were measured by quantitative real-time PCR (qRT-PCR). The expression of actin skeletal protein 1 (LASP1) was evaluated by Western blot analysis. Flow cytometry assays, transwell assays, colony formation assay, and cell counting kit-8 (CCK-8) assay were used to evaluate the roles of miR-125a-5p and CYTOR in HCC cells. The target genes of CYTOR and miR-125a-5p were identified by bioinformatics analysis and Luciferase assay. CYTOR was upregulated in HCC cell lines, and knockdown of CYTOR inhibited HCC cell growth. MiR-125a-5p was downregulated in HCC cells and a target of CYTOR in regulating HCC progression. Furthermore, LASP1 was a downstream target of miR-125a-5p. Finally, CYTOR was found to be involved in HCC progression &lt;i>in vivo&lt;/i>. CYTOR promotes HCC development by regulating the miR-125a-5p/LASP1 axis.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-05T00:27:52.871Z</modification><creation>2025-04-05T00:27:52.871Z</creation></dates><accession>S-EPMC8974008</accession><cross_references><pubmed>35081873</pubmed><doi>10.1080/21655979.2021.2024328</doi></cross_references></HashMap>