<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mao X</submitter><funding>Shaanxi Provincial Science and Technology Department</funding><funding>National Natural Science Foundation of China</funding><funding>Xi&amp;amp;apos;an Jiaotong University</funding><pagination>207-219</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12627352</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>77</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Ferroptosis is an iron-dependent form of cell death triggered by the excessive accumulation of lipid peroxides. Understanding the regulatory mechanisms of ferroptosis and developing strategies to target this process hold significant clinical applications in tumor therapy.&lt;h4>Objective&lt;/h4>Our study aims to search for novel candidate genes involved in the regulation of ferroptosis and to investigate their mechanism of action in ferroptosis and tumor therapy.&lt;h4>Methods&lt;/h4>We employed a CRISPR-Cas9 library to perform a genome-wide screen under ferroptosis inducer treatment conditions, revealing Scavenger Receptor Class B Member 1(SCARB1) as a novel candidate gene involved in ferroptosis regulation. Subsequently, lipidomic analyses, metabolic interventions, and relevant </pubmed_abstract><journal>Journal of advanced research</journal><pubmed_title>SCARB1 links cholesterol metabolism-mediated ferroptosis inhibition to radioresistance in tumor cells.</pubmed_title><pmcid>PMC12627352</pmcid><funding_grant_id>82103272</funding_grant_id><funding_grant_id>2024JC-TBZC-13</funding_grant_id><funding_grant_id>82372847</funding_grant_id><funding_grant_id>QCYRCXM-2022-166</funding_grant_id><funding_grant_id>2022KW-48</funding_grant_id><funding_grant_id>QCYRCXM-2022-142</funding_grant_id><pubmed_authors>Xiong J</pubmed_authors><pubmed_authors>Cai M</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Xiao Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Mao X</pubmed_authors><pubmed_authors>He Q</pubmed_authors><pubmed_authors>Han S</pubmed_authors></additional><is_claimable>false</is_claimable><name>SCARB1 links cholesterol metabolism-mediated ferroptosis inhibition to radioresistance in tumor cells.</name><description>&lt;h4>Introduction&lt;/h4>Ferroptosis is an iron-dependent form of cell death triggered by the excessive accumulation of lipid peroxides. Understanding the regulatory mechanisms of ferroptosis and developing strategies to target this process hold significant clinical applications in tumor therapy.&lt;h4>Objective&lt;/h4>Our study aims to search for novel candidate genes involved in the regulation of ferroptosis and to investigate their mechanism of action in ferroptosis and tumor therapy.&lt;h4>Methods&lt;/h4>We employed a CRISPR-Cas9 library to perform a genome-wide screen under ferroptosis inducer treatment conditions, revealing Scavenger Receptor Class B Member 1(SCARB1) as a novel candidate gene involved in ferroptosis regulation. Subsequently, lipidomic analyses, metabolic interventions, and relevant </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T18:43:37.598Z</modification><creation>2026-05-20T03:13:59.983Z</creation></dates><accession>S-EPMC12627352</accession><cross_references><pubmed>39832721</pubmed><doi>10.1016/j.jare.2025.01.026</doi></cross_references></HashMap>