<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Li X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The histone chaperone Holliday Junction Recognition Protein (HJURP) has been associated with multiple types of cancers, but its role in GC is not yet fully understood. Considering its functions in centromere stability and DNA repair, investigating HJURP's role in GC may offer novel therapeutic perspectives.&lt;h4>Methods&lt;/h4>HJURP expression was examined in a dataset comprising TCGA-STAD samples and an internal group of GC patients, utilizing RNA sequencing and Western blot techniques. Functional experiments were carried out on the AGS and HGC-27 GC cell lines. The expression levels of HJURP, MYC, and Topoisomerase II alpha (TOP2A) were assessed via quantitative real-time PCR and Western blot. Proliferation rates of the cells were determined through EdU, CCK-8, and colony f</pubmed_abstract><journal>Frontiers in molecular biosciences</journal><pagination>1566293</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12021643</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>HJURP modulates cell proliferation and chemoresistance via the MYC/TOP2A transcriptional axis in gastric cancer.</pubmed_title><pmcid>PMC12021643</pmcid><pubmed_authors>Ma P</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Ren Y</pubmed_authors><pubmed_authors>Gao S</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Mao Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>HJURP modulates cell proliferation and chemoresistance via the MYC/TOP2A transcriptional axis in gastric cancer.</name><description>&lt;h4>Background&lt;/h4>The histone chaperone Holliday Junction Recognition Protein (HJURP) has been associated with multiple types of cancers, but its role in GC is not yet fully understood. Considering its functions in centromere stability and DNA repair, investigating HJURP's role in GC may offer novel therapeutic perspectives.&lt;h4>Methods&lt;/h4>HJURP expression was examined in a dataset comprising TCGA-STAD samples and an internal group of GC patients, utilizing RNA sequencing and Western blot techniques. Functional experiments were carried out on the AGS and HGC-27 GC cell lines. The expression levels of HJURP, MYC, and Topoisomerase II alpha (TOP2A) were assessed via quantitative real-time PCR and Western blot. Proliferation rates of the cells were determined through EdU, CCK-8, and colony f</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-04-08T19:01:50.532Z</modification><creation>2025-07-03T03:04:17.089Z</creation></dates><accession>S-EPMC12021643</accession><cross_references><pubmed>40290723</pubmed><doi>10.3389/fmolb.2025.1566293</doi></cross_references></HashMap>