<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mooney B</submitter><funding>Stand Up To Cancer</funding><funding>Michael Smith Health Research BC</funding><funding>BC Cancer Foundation</funding><funding>St. Baldrick&amp;apos;s Foundation</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>Cancer Prevention and Research Institute of Texas</funding><funding>Canadian Institutes of Health Research</funding><pagination>1022-1037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10905525</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(5)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Ewing sarcoma is the second most common bone sarcoma in children, with 1 case per 1.5 million in the United States. Although the survival rate of patients diagnosed with localized disease is approximately 70%, this decreases to approximately 30% for patients with metastatic disease and only approximately 10% for treatment-refractory disease, which have not changed for decades. Therefore, new therapeutic strategies are urgently needed for metastatic and refractory Ewing sarcoma.&lt;h4>Experimental design&lt;/h4>This study analyzed 19 unique Ewing sarcoma patient- or cell line-derived xenografts (from 14 primary and 5 metastatic specimens) using proteomics to identify surface proteins for potential immunotherapeutic targeting. Plasma membranes were enriched using density gradient u</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Surface and Global Proteome Analyses Identify ENPP1 and Other Surface Proteins as Actionable Immunotherapeutic Targets in Ewing Sarcoma.</pubmed_title><pmcid>PMC10905525</pmcid><funding_grant_id>UO1CA263981</funding_grant_id><funding_grant_id>SU2C-AACR-DT1113</funding_grant_id><funding_grant_id>R35 CA220500</funding_grant_id><funding_grant_id>1U54CA232568-01</funding_grant_id><funding_grant_id>U01 CA263981</funding_grant_id><funding_grant_id>R35CA220500</funding_grant_id><funding_grant_id>RP160716</funding_grant_id><funding_grant_id>T32 CA009140</funding_grant_id><funding_grant_id>CA009140</funding_grant_id><funding_grant_id>U54 CA232568</funding_grant_id><funding_grant_id>415377</funding_grant_id><funding_grant_id>18569</funding_grant_id><funding_grant_id>RT-2023-3194</funding_grant_id><pubmed_authors>Shraim R</pubmed_authors><pubmed_authors>Lizardo MM</pubmed_authors><pubmed_authors>Maris JM</pubmed_authors><pubmed_authors>Sorensen PH</pubmed_authors><pubmed_authors>Mooney B</pubmed_authors><pubmed_authors>Dimitrov DS</pubmed_authors><pubmed_authors>Spencer Miko SE</pubmed_authors><pubmed_authors>El-Naggar AM</pubmed_authors><pubmed_authors>Houghton PJ</pubmed_authors><pubmed_authors>Zhang HF</pubmed_authors><pubmed_authors>Delaidelli A</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Kurmasheva RT</pubmed_authors><pubmed_authors>Hughes CS</pubmed_authors><pubmed_authors>Diskin SJ</pubmed_authors><pubmed_authors>Negri GL</pubmed_authors><pubmed_authors>Shyp T</pubmed_authors><pubmed_authors>Weiner AK</pubmed_authors><pubmed_authors>Morin GB</pubmed_authors><pubmed_authors>Li A</pubmed_authors><pubmed_authors>Radaoui AB</pubmed_authors><pubmed_authors>Rouleau M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Surface and Global Proteome Analyses Identify ENPP1 and Other Surface Proteins as Actionable Immunotherapeutic Targets in Ewing Sarcoma.</name><description>&lt;h4>Purpose&lt;/h4>Ewing sarcoma is the second most common bone sarcoma in children, with 1 case per 1.5 million in the United States. Although the survival rate of patients diagnosed with localized disease is approximately 70%, this decreases to approximately 30% for patients with metastatic disease and only approximately 10% for treatment-refractory disease, which have not changed for decades. Therefore, new therapeutic strategies are urgently needed for metastatic and refractory Ewing sarcoma.&lt;h4>Experimental design&lt;/h4>This study analyzed 19 unique Ewing sarcoma patient- or cell line-derived xenografts (from 14 primary and 5 metastatic specimens) using proteomics to identify surface proteins for potential immunotherapeutic targeting. Plasma membranes were enriched using density gradient u</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-08T06:07:57.377Z</modification><creation>2025-05-29T20:46:31.097Z</creation></dates><accession>S-EPMC10905525</accession><cross_references><pubmed>37812652</pubmed><doi>10.1158/1078-0432.CCR-23-2187</doi></cross_references></HashMap>