<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Du R</submitter><funding>National Natural Science Foundation of China</funding><funding>the Doctoral Research Start-up Fund Project of Nanyang Institute of Technology</funding><funding>the Talent Program of Central China：Science and Technology Innovation Leading Talent</funding><funding>the Science and Technology Project of Henan Province</funding><pagination>9167</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11035576</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Syndecan-binding protein (SDCBP) was reported to stimulate the advancement of esophageal squamous cell carcinoma (ESCC) and could potentially be a target for ESCC treatment. There is a growing corpus of research on the anti-tumor effects of iron chelators; however, very few studies have addressed the involvement of dexrazoxane in cancer. In this study, structure-based virtual screening was employed to select drugs targeting SDCBP from the Food and Drug Administration (FDA)-approved drug databases. The sepharose 4B beads pull-down assay revealed that dexrazoxane targeted SDCBP by interacting with its PDZ1 domain. Additionally, dexrazoxane inhibited ESCC cell proliferation and anchorage-independent colony formation via SDCBP. ESCC cell apoptosis and G2 phase arrest were induced as measured b</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Dexrazoxane inhibits the growth of esophageal squamous cell carcinoma by attenuating SDCBP/MDA-9/syntenin-mediated EGFR-PI3K-Akt pathway activation.</pubmed_title><pmcid>PMC11035576</pmcid><funding_grant_id>82273058</funding_grant_id><funding_grant_id>234200510006</funding_grant_id><funding_grant_id>NGBJ-2022-05</funding_grant_id><funding_grant_id>82002592</funding_grant_id><funding_grant_id>222102310156</funding_grant_id><pubmed_authors>Xiao N</pubmed_authors><pubmed_authors>Du R</pubmed_authors><pubmed_authors>Guo K</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Bian H</pubmed_authors><pubmed_authors>Li K</pubmed_authors><pubmed_authors>Zhou Z</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dexrazoxane inhibits the growth of esophageal squamous cell carcinoma by attenuating SDCBP/MDA-9/syntenin-mediated EGFR-PI3K-Akt pathway activation.</name><description>Syndecan-binding protein (SDCBP) was reported to stimulate the advancement of esophageal squamous cell carcinoma (ESCC) and could potentially be a target for ESCC treatment. There is a growing corpus of research on the anti-tumor effects of iron chelators; however, very few studies have addressed the involvement of dexrazoxane in cancer. In this study, structure-based virtual screening was employed to select drugs targeting SDCBP from the Food and Drug Administration (FDA)-approved drug databases. The sepharose 4B beads pull-down assay revealed that dexrazoxane targeted SDCBP by interacting with its PDZ1 domain. Additionally, dexrazoxane inhibited ESCC cell proliferation and anchorage-independent colony formation via SDCBP. ESCC cell apoptosis and G2 phase arrest were induced as measured b</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-03T01:31:52.457Z</modification><creation>2026-04-22T03:13:24.615Z</creation></dates><accession>S-EPMC11035576</accession><cross_references><pubmed>38649770</pubmed><doi>10.1038/s41598-024-59665-5</doi></cross_references></HashMap>