<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Guo Q</submitter><funding>Wu Jieping Medical Foundation</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Breast cancer (BC) is considered to be one of the primary causes of cancer deaths in women. Cuproptosis was suggested to play an important role in tumor proliferation and tumor immune microenvironment. Therefore, an investigation was conducted to identify the relationship between cuproptosis-related long non-coding RNAs (lncRNAs) and BC prognosis.&lt;h4>Method&lt;/h4>Based on The Cancer Genome Atlas (TCGA), nine cuproptosis-related lncRNAs were identified by Pearson's analysis and Cox regression analysis to create a cuproptosis-related lncRNA signature. Subsequently, patients with BC were divided into high-risk and low-risk groups. The Kaplan-Meier curves and a time-dependent receiver operating characteristic (ROC) analysis were employed to elucidate the predictive capability </pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1081089</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9815178</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comprehensive analysis of cuproptosis-related long non-coding RNA signature and personalized therapeutic strategy of breast cancer patients.</pubmed_title><pmcid>PMC9815178</pmcid><pubmed_authors>Qiu P</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Guo Q</pubmed_authors><pubmed_authors>Pan K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comprehensive analysis of cuproptosis-related long non-coding RNA signature and personalized therapeutic strategy of breast cancer patients.</name><description>&lt;h4>Background&lt;/h4>Breast cancer (BC) is considered to be one of the primary causes of cancer deaths in women. Cuproptosis was suggested to play an important role in tumor proliferation and tumor immune microenvironment. Therefore, an investigation was conducted to identify the relationship between cuproptosis-related long non-coding RNAs (lncRNAs) and BC prognosis.&lt;h4>Method&lt;/h4>Based on The Cancer Genome Atlas (TCGA), nine cuproptosis-related lncRNAs were identified by Pearson's analysis and Cox regression analysis to create a cuproptosis-related lncRNA signature. Subsequently, patients with BC were divided into high-risk and low-risk groups. The Kaplan-Meier curves and a time-dependent receiver operating characteristic (ROC) analysis were employed to elucidate the predictive capability </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-29T20:14:56.517Z</modification><creation>2025-04-04T12:37:12.35Z</creation></dates><accession>S-EPMC9815178</accession><cross_references><pubmed>36620596</pubmed><doi>10.3389/fonc.2022.1081089</doi></cross_references></HashMap>