<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Delaney S</submitter><funding>NIAID NIH HHS</funding><funding>Foundation for the National Institutes of Health</funding><funding>NCI NIH HHS</funding><pagination>2547-2557</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11223962</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(9)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Cadherin-17 (CDH17) is a calcium-dependent cell adhesion protein that is overexpressed in several adenocarcinomas, including gastric, colorectal, and pancreatic adenocarcinoma. High levels of CDH17 have been linked to metastatic disease and poor prognoses in patients with these malignancies, fueling interest in the protein as a target for diagnostics and therapeutics. Herein, we report the synthesis, in vitro validation, and in vivo evaluation of a CDH17-targeted &lt;sup>89&lt;/sup>Zr-labeled immunoPET probe.&lt;h4>Methods&lt;/h4>The CDH17-targeting mAb D2101 was modified with an isothiocyanate-bearing derivative of desferrioxamine (DFO) to produce a chelator-bearing immunoconjugate - DFO-D2101 - and flow cytometry and surface plasmon resonance (SPR) were used to interrogate its antige</pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pubmed_title>Cadherin-17 as a target for the immunoPET of adenocarcinoma.</pubmed_title><pmcid>PMC11223962</pmcid><funding_grant_id>R00CA226363</funding_grant_id><funding_grant_id>R01 CA244327</funding_grant_id><funding_grant_id>1R01AI175417</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>1R01CA281801</funding_grant_id><funding_grant_id>1R01CA244327</funding_grant_id><funding_grant_id>R01 CA204167</funding_grant_id><funding_grant_id>R01CA240963</funding_grant_id><funding_grant_id>R01 AI175417</funding_grant_id><funding_grant_id>R00ES034053</funding_grant_id><funding_grant_id>R01 CA240963</funding_grant_id><funding_grant_id>R01 CA281801</funding_grant_id><funding_grant_id>F31CA275334</funding_grant_id><pubmed_authors>Lam D</pubmed_authors><pubmed_authors>Keinanen O</pubmed_authors><pubmed_authors>Delaney S</pubmed_authors><pubmed_authors>Wolfe AL</pubmed_authors><pubmed_authors>Zeglis BM</pubmed_authors><pubmed_authors>Hamakubo T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cadherin-17 as a target for the immunoPET of adenocarcinoma.</name><description>&lt;h4>Purpose&lt;/h4>Cadherin-17 (CDH17) is a calcium-dependent cell adhesion protein that is overexpressed in several adenocarcinomas, including gastric, colorectal, and pancreatic adenocarcinoma. High levels of CDH17 have been linked to metastatic disease and poor prognoses in patients with these malignancies, fueling interest in the protein as a target for diagnostics and therapeutics. Herein, we report the synthesis, in vitro validation, and in vivo evaluation of a CDH17-targeted &lt;sup>89&lt;/sup>Zr-labeled immunoPET probe.&lt;h4>Methods&lt;/h4>The CDH17-targeting mAb D2101 was modified with an isothiocyanate-bearing derivative of desferrioxamine (DFO) to produce a chelator-bearing immunoconjugate - DFO-D2101 - and flow cytometry and surface plasmon resonance (SPR) were used to interrogate its antige</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-02T21:18:36.347Z</modification><creation>2025-04-04T12:21:36.052Z</creation></dates><accession>S-EPMC11223962</accession><cross_references><pubmed>38625402</pubmed><doi>10.1007/s00259-024-06709-7</doi></cross_references></HashMap>