<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2024</volume><submitter>Li Z</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Neuroblastoma (NB) is one of the most devastating malignancies in children, accounting for a high mortality rate due to limited treatment options. This study is aimed at elucidating the role of the ferroptosis-related EIF2S1 gene in NB pathogenesis and exploring its potential as a therapeutic target. &lt;b>Methods:&lt;/b> We conducted comprehensive bioinformatics analyses utilizing the FerrDb database and NB-related transcriptomics data to investigate the role of EIF2S1 in NB. Changes in EIF2S1 expression were subsequently validated in NB tissues and cell lines. Loss-of-function experiments were performed in SK-N-SH and IMR-32 cell lines through shRNA-mediated EIF2S1 knockdown. The impact of EIF2S1 knockdown on the tumorigenesis of SK-N-SH cells was assessed in nude mice. &lt;b>R</pubmed_abstract><journal>International journal of genomics</journal><pagination>6594426</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11512646</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>EIF2S1 Silencing Impedes Neuroblastoma Development Through GPX4 Inactivation and Ferroptosis Induction.</pubmed_title><pmcid>PMC11512646</pmcid><pubmed_authors>Liang S</pubmed_authors><pubmed_authors>Yuan T</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>EIF2S1 Silencing Impedes Neuroblastoma Development Through GPX4 Inactivation and Ferroptosis Induction.</name><description>&lt;b>Background:&lt;/b> Neuroblastoma (NB) is one of the most devastating malignancies in children, accounting for a high mortality rate due to limited treatment options. This study is aimed at elucidating the role of the ferroptosis-related EIF2S1 gene in NB pathogenesis and exploring its potential as a therapeutic target. &lt;b>Methods:&lt;/b> We conducted comprehensive bioinformatics analyses utilizing the FerrDb database and NB-related transcriptomics data to investigate the role of EIF2S1 in NB. Changes in EIF2S1 expression were subsequently validated in NB tissues and cell lines. Loss-of-function experiments were performed in SK-N-SH and IMR-32 cell lines through shRNA-mediated EIF2S1 knockdown. The impact of EIF2S1 knockdown on the tumorigenesis of SK-N-SH cells was assessed in nude mice. &lt;b>R</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-04-08T18:38:55.622Z</modification><creation>2025-04-06T14:21:59.141Z</creation></dates><accession>S-EPMC11512646</accession><cross_references><pubmed>39465005</pubmed><doi>10.1155/2024/6594426</doi></cross_references></HashMap>