<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Yuan Y</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>The purpose of our research was to investigate the clinical significance of lncRNA VIM anti-sense 1 (VIM-AS1) and to elucidate its cellular functions in breast cancer patients.&lt;h4>Methods&lt;/h4>A cohort of one hundred and twenty-one individuals diagnosed with breast cancer and 95 healthy volunteers were recruited for this study. Relative abundances of VIM-AS1 were detected through quantitative real-time polymerase chain reaction (qRT-PCR). Receiver operating characteristic (ROC) was employed for evaluating the diagnosis potential of VIM-AS1. Kaplan-Meier method and Cox regression analysis was performed to further examine the prognostic performance of VIM-AS1. The cellular events of VIM-AS1 were assessed via CCK-8 and Transwell assay. The target interaction of VIM-AS1 and mi</pubmed_abstract><journal>Discover oncology</journal><pagination>1807</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12495003</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>LncRNA VIM-AS1 is a potential prognostic biomarker and effects on tumor cellular behaviors in breast cancer via impairing miR-29a-3p.</pubmed_title><pmcid>PMC12495003</pmcid><pubmed_authors>Wei M</pubmed_authors><pubmed_authors>Kong L</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Yuan Q</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Bian W</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>LncRNA VIM-AS1 is a potential prognostic biomarker and effects on tumor cellular behaviors in breast cancer via impairing miR-29a-3p.</name><description>&lt;h4>Objective&lt;/h4>The purpose of our research was to investigate the clinical significance of lncRNA VIM anti-sense 1 (VIM-AS1) and to elucidate its cellular functions in breast cancer patients.&lt;h4>Methods&lt;/h4>A cohort of one hundred and twenty-one individuals diagnosed with breast cancer and 95 healthy volunteers were recruited for this study. Relative abundances of VIM-AS1 were detected through quantitative real-time polymerase chain reaction (qRT-PCR). Receiver operating characteristic (ROC) was employed for evaluating the diagnosis potential of VIM-AS1. Kaplan-Meier method and Cox regression analysis was performed to further examine the prognostic performance of VIM-AS1. The cellular events of VIM-AS1 were assessed via CCK-8 and Transwell assay. The target interaction of VIM-AS1 and mi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-05-31T03:16:15.799Z</modification><creation>2026-05-31T03:06:42.246Z</creation></dates><accession>S-EPMC12495003</accession><cross_references><pubmed>41042406</pubmed><doi>10.1007/s12672-025-03568-y</doi></cross_references></HashMap>