<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Talebian H</submitter><funding>New Frontiers in Research Fund - Transformation</funding><pagination>11651</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12692291</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(23)</volume><pubmed_abstract>Prostate cancer (PCa), particularly in its metastatic form, remains a major clinical challenge due to limited diagnostic and therapeutic options. To address this, we developed a novel radiotheranostic agent, [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP-PSMA, by conjugating a prostate-specific membrane antigen (PSMA) ligand to a &lt;sup>64&lt;/sup>Cu-radiolabeled terpyridine-platinum (TP) compound previously shown to exert selective cytotoxicity against cancer cells. In this study, the biological performance of [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP-PSMA was compared with the monomeric analogs [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-PSMA and [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP through in vitro studies in PSMA-positive LNCaP prostate cancer cells and non-malignant HEK-293 cells. [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP-PSMA showed high stability, PSMA binding </pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Development and In Vitro Evaluation of [&amp;lt;sup&amp;gt;64&amp;lt;/sup&amp;gt;Cu]Cu-NOTA-TP-PSMA, a Novel Radiotheranostic Agent Against Prostate Cancer.</pubmed_title><pmcid>PMC12692291</pmcid><funding_grant_id>NFRFT-2022-00269</funding_grant_id><pubmed_authors>Ignatius Arokia Doss PM</pubmed_authors><pubmed_authors>Ait-Mohand S</pubmed_authors><pubmed_authors>Talebian H</pubmed_authors><pubmed_authors>Sanche L</pubmed_authors><pubmed_authors>Guerin B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and In Vitro Evaluation of [&amp;lt;sup&amp;gt;64&amp;lt;/sup&amp;gt;Cu]Cu-NOTA-TP-PSMA, a Novel Radiotheranostic Agent Against Prostate Cancer.</name><description>Prostate cancer (PCa), particularly in its metastatic form, remains a major clinical challenge due to limited diagnostic and therapeutic options. To address this, we developed a novel radiotheranostic agent, [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP-PSMA, by conjugating a prostate-specific membrane antigen (PSMA) ligand to a &lt;sup>64&lt;/sup>Cu-radiolabeled terpyridine-platinum (TP) compound previously shown to exert selective cytotoxicity against cancer cells. In this study, the biological performance of [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP-PSMA was compared with the monomeric analogs [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-PSMA and [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP through in vitro studies in PSMA-positive LNCaP prostate cancer cells and non-malignant HEK-293 cells. [&lt;sup>64&lt;/sup>Cu]Cu-NOTA-TP-PSMA showed high stability, PSMA binding </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-05-26T11:01:42.72Z</modification><creation>2026-05-24T03:11:15.956Z</creation></dates><accession>S-EPMC12692291</accession><cross_references><pubmed>41373803</pubmed><doi>10.3390/ijms262311651</doi></cross_references></HashMap>