<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sinha A</submitter><funding>Congressionally Directed Medical Research Programs</funding><funding>NCI NIH HHS</funding><pagination>493</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12899641</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(3)</volume><pubmed_abstract>Prostate cancer is the third-leading cause of cancer death in men. Prostate-specific membrane antigen (PSMA) is a robust biomarker that is expressed in approximately 80% of patients diagnosed with prostate cancer; several theranostic strategies have emerged based upon targeting this biomarker. This report describes a dimeric aptamer complex (DAC) which is selective for PSMA&lt;sup>+&lt;/sup> cancer cells and is amenable to derivatization with additional diagnostic and therapeutic molecules. Confocal microscopy confirmed the selective nature of the DAC for PSMA&lt;sup>+&lt;/sup> LNCAP tumor cells. In addition, the affinity of the DAC for the PSMA protein was determined to be 2.16 ± 0.15 nM using biolayer interferometry (BLI). In proof-of-principle studies, this DAC was biotinylated (BioDAC; A10), compl</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Preclinical Evaluation of a Radiolabeled Anti-PSMA Dimeric Aptamer in a Murine Model of Human Prostate Cancer.</pubmed_title><pmcid>PMC12899641</pmcid><funding_grant_id>R21-CA219899</funding_grant_id><funding_grant_id>W81XWH-19-1-0046</funding_grant_id><funding_grant_id>R21-CA227709</funding_grant_id><pubmed_authors>Sinha A</pubmed_authors><pubmed_authors>Pandya DN</pubmed_authors><pubmed_authors>Eeka P</pubmed_authors><pubmed_authors>Wadas TJ</pubmed_authors><pubmed_authors>Boyacioglu O</pubmed_authors><pubmed_authors>Gmeiner WH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preclinical Evaluation of a Radiolabeled Anti-PSMA Dimeric Aptamer in a Murine Model of Human Prostate Cancer.</name><description>Prostate cancer is the third-leading cause of cancer death in men. Prostate-specific membrane antigen (PSMA) is a robust biomarker that is expressed in approximately 80% of patients diagnosed with prostate cancer; several theranostic strategies have emerged based upon targeting this biomarker. This report describes a dimeric aptamer complex (DAC) which is selective for PSMA&lt;sup>+&lt;/sup> cancer cells and is amenable to derivatization with additional diagnostic and therapeutic molecules. Confocal microscopy confirmed the selective nature of the DAC for PSMA&lt;sup>+&lt;/sup> LNCAP tumor cells. In addition, the affinity of the DAC for the PSMA protein was determined to be 2.16 ± 0.15 nM using biolayer interferometry (BLI). In proof-of-principle studies, this DAC was biotinylated (BioDAC; A10), compl</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-08T03:16:39.54Z</modification><creation>2026-07-08T03:08:39.87Z</creation></dates><accession>S-EPMC12899641</accession><cross_references><pubmed>41683470</pubmed><doi>10.3390/molecules31030493</doi></cross_references></HashMap>