<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zheleznyak A</submitter><funding>NIBIB NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><funding>NIH HHS</funding><pagination>738-752</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11282151</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(4)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Multiple myeloma (MM) affects over 35,000 patients each year in the US. There remains a need for versatile Positron Emission Tomography (PET) tracers for the detection, accurate staging, and monitoring of treatment response of MM that have optimal specificity and translational attributes. CD38 is uniformly overexpressed in MM and thus represents an ideal target to develop CD38-targeted small molecule PET radiopharmaceuticals to address these challenges.&lt;h4>Procedures&lt;/h4>Using phage display peptide libraries and pioneering algorithms, we identified novel CD38 specific peptides. Imaging bioconjugates were synthesized using solid phase peptide chemistry, and systematically analyzed in vitro and in vivo in relevant MM systems.&lt;h4>Results&lt;/h4>The CD38-targeted bioconjugates wer</pubmed_abstract><journal>Molecular imaging and biology</journal><pubmed_title>Development of New CD38 Targeted Peptides for Cancer Imaging.</pubmed_title><pmcid>PMC11282151</pmcid><funding_grant_id>T32 EB014855</funding_grant_id><funding_grant_id>R01 CA248493</funding_grant_id><funding_grant_id>P30 CA091842</funding_grant_id><funding_grant_id>R42 CA257797</funding_grant_id><funding_grant_id>S10 OD027042</funding_grant_id><funding_grant_id>S10 OD025264</funding_grant_id><funding_grant_id>R01 CA176221</funding_grant_id><funding_grant_id>R01 CA260855</funding_grant_id><funding_grant_id>P50 CA094056</funding_grant_id><pubmed_authors>Duncan K</pubmed_authors><pubmed_authors>Prior J</pubmed_authors><pubmed_authors>Ghai A</pubmed_authors><pubmed_authors>Vanover A</pubmed_authors><pubmed_authors>Zheleznyak A</pubmed_authors><pubmed_authors>Achilefu S</pubmed_authors><pubmed_authors>Lees S</pubmed_authors><pubmed_authors>Xu B</pubmed_authors><pubmed_authors>Manion B</pubmed_authors><pubmed_authors>Liang K</pubmed_authors><pubmed_authors>Tang R</pubmed_authors><pubmed_authors>Shokeen M</pubmed_authors><pubmed_authors>Kelly K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of New CD38 Targeted Peptides for Cancer Imaging.</name><description>&lt;h4>Purpose&lt;/h4>Multiple myeloma (MM) affects over 35,000 patients each year in the US. There remains a need for versatile Positron Emission Tomography (PET) tracers for the detection, accurate staging, and monitoring of treatment response of MM that have optimal specificity and translational attributes. CD38 is uniformly overexpressed in MM and thus represents an ideal target to develop CD38-targeted small molecule PET radiopharmaceuticals to address these challenges.&lt;h4>Procedures&lt;/h4>Using phage display peptide libraries and pioneering algorithms, we identified novel CD38 specific peptides. Imaging bioconjugates were synthesized using solid phase peptide chemistry, and systematically analyzed in vitro and in vivo in relevant MM systems.&lt;h4>Results&lt;/h4>The CD38-targeted bioconjugates wer</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-05-02T03:36:33.963Z</modification><creation>2026-04-07T17:35:59.206Z</creation></dates><accession>S-EPMC11282151</accession><cross_references><pubmed>38480650</pubmed><doi>10.1007/s11307-024-01901-5</doi></cross_references></HashMap>