<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Behr SC</submitter><funding>UCSF Academic Senate</funding><funding>American Brain Tumor Association</funding><funding>National Institutes of Health</funding><pagination>93999</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6238742</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(21)</volume><pubmed_abstract>Noninvasive tools that target tumor cells could improve the management of glioma. Cancer generally has a high demand for Fe(III), an essential nutrient for a variety of biochemical processes. We tested whether 68Ga-citrate, an Fe(III) biomimetic that binds to apo-transferrin in blood, detects glioma in preclinical models and patients using hybrid PET/MRI. Mouse PET/CT studies showed that 68Ga-citrate accumulates in subcutaneous U87MG xenografts in a transferrin receptor-dependent fashion within 4 hours after injection. Seventeen patients with WHO grade III or IV glioma received 3.7-10.2 mCi 68Ga-citrate and were imaged with PET/MR 123-307 minutes after injection to establish that the radiotracer can localize to human tumors. Multiple contrast-enhancing lesions were PET avid, and tumor to a</pubmed_abstract><journal>JCI insight</journal><pubmed_title>Targeting iron metabolism in high-grade glioma with 68Ga-citrate PET/MR.</pubmed_title><pmcid>PMC6238742</pmcid><funding_grant_id>N/A</funding_grant_id><funding_grant_id>P30CA082103</funding_grant_id><funding_grant_id>R01CA166766</funding_grant_id><funding_grant_id>P50CA097257</funding_grant_id><funding_grant_id>R01CA154561</funding_grant_id><funding_grant_id>R01CA17661</funding_grant_id><funding_grant_id>DG1700008</funding_grant_id><funding_grant_id>T32EB001631</funding_grant_id><pubmed_authors>Behr SC</pubmed_authors><pubmed_authors>Gao KT</pubmed_authors><pubmed_authors>Nelson SJ</pubmed_authors><pubmed_authors>Wang YH</pubmed_authors><pubmed_authors>Ma W</pubmed_authors><pubmed_authors>Cha S</pubmed_authors><pubmed_authors>Evans MJ</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Seo Y</pubmed_authors><pubmed_authors>Moroz A</pubmed_authors><pubmed_authors>Lee JK</pubmed_authors><pubmed_authors>Hsiao JC</pubmed_authors><pubmed_authors>Wilson DM</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Villanueva-Meyer JE</pubmed_authors><pubmed_authors>Chang SM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting iron metabolism in high-grade glioma with 68Ga-citrate PET/MR.</name><description>Noninvasive tools that target tumor cells could improve the management of glioma. Cancer generally has a high demand for Fe(III), an essential nutrient for a variety of biochemical processes. We tested whether 68Ga-citrate, an Fe(III) biomimetic that binds to apo-transferrin in blood, detects glioma in preclinical models and patients using hybrid PET/MRI. Mouse PET/CT studies showed that 68Ga-citrate accumulates in subcutaneous U87MG xenografts in a transferrin receptor-dependent fashion within 4 hours after injection. Seventeen patients with WHO grade III or IV glioma received 3.7-10.2 mCi 68Ga-citrate and were imaged with PET/MR 123-307 minutes after injection to establish that the radiotracer can localize to human tumors. Multiple contrast-enhancing lesions were PET avid, and tumor to a</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2025-04-05T12:27:28.341Z</modification><creation>2019-03-27T00:08:32Z</creation></dates><accession>S-EPMC6238742</accession><cross_references><pubmed>30385712</pubmed><doi>10.1172/jci.insight.93999</doi></cross_references></HashMap>