<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Anderson AN</submitter><funding>Melanoma Research Foundation</funding><funding>American Association for Cancer Research Ocular Melanoma Foundation</funding><funding>U.S. National Library of Medicine</funding><funding>National Institutes of Health</funding><funding>National Human Genome Research Institute</funding><funding>National Cancer Institute, United States</funding><funding>Center for Cancer Research</funding><funding>CCR NIH HHS</funding><funding>Medical Research Foundation</funding><funding>Melanoma Research Foundation Medical Student Award</funding><funding>Malcolm M. Marquis, MD Endowed Fund for Innovation</funding><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NLM NIH HHS</funding><funding>NIH HHS</funding><pagination>67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11264923</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Uveal melanoma is the most common non-cutaneous melanoma and is an intraocular malignancy affecting nearly 7,000 individuals per year worldwide. Of these, approximately 50% will progress to metastatic disease for which there are currently no effective curative therapies. Despite advances in molecular profiling and metastatic stratification of uveal melanoma tumors, little is known regarding their underlying biology of metastasis. Our group has identified a disseminated neoplastic cell population characterized by co-expression of immune and melanoma proteins, circulating hybrid cells (hybrids), in patients with uveal melanoma. Compared to circulating tumor cells, which lack expression of immune proteins, hybrids are detected at an increased prevalence in peripheral blood </pubmed_abstract><journal>Biomarker research</journal><pubmed_title>Detection of neoplastic-immune hybrid cells with metastatic properties in uveal melanoma.</pubmed_title><pmcid>PMC11264923</pmcid><funding_grant_id>P30CA069533</funding_grant_id><funding_grant_id>U24 HG012198</funding_grant_id><funding_grant_id>T32GM141938</funding_grant_id><funding_grant_id>U41 HG003751</funding_grant_id><funding_grant_id>5U01CA23906</funding_grant_id><funding_grant_id>T15 LM007088</funding_grant_id><funding_grant_id>5U41HG003751</funding_grant_id><funding_grant_id>P30 CA069533</funding_grant_id><funding_grant_id>5T15LM007088</funding_grant_id><funding_grant_id>R44 CA250861</funding_grant_id><funding_grant_id>U01 CA239069</funding_grant_id><funding_grant_id>P30 EY010572</funding_grant_id><funding_grant_id>F31CA271676</funding_grant_id><funding_grant_id>R44CA250861</funding_grant_id><pubmed_authors>Sengupta SK</pubmed_authors><pubmed_authors>Jones JA</pubmed_authors><pubmed_authors>Fan Y</pubmed_authors><pubmed_authors>Pang A</pubmed_authors><pubmed_authors>Wu G</pubmed_authors><pubmed_authors>Skalet AH</pubmed_authors><pubmed_authors>Wong MH</pubmed_authors><pubmed_authors>Farley HC</pubmed_authors><pubmed_authors>Klocke CD</pubmed_authors><pubmed_authors>Conley P</pubmed_authors><pubmed_authors>Dawson AD</pubmed_authors><pubmed_authors>Anderson AN</pubmed_authors><pubmed_authors>Gillingham AR</pubmed_authors><pubmed_authors>Gibbs SL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detection of neoplastic-immune hybrid cells with metastatic properties in uveal melanoma.</name><description>&lt;h4>Background&lt;/h4>Uveal melanoma is the most common non-cutaneous melanoma and is an intraocular malignancy affecting nearly 7,000 individuals per year worldwide. Of these, approximately 50% will progress to metastatic disease for which there are currently no effective curative therapies. Despite advances in molecular profiling and metastatic stratification of uveal melanoma tumors, little is known regarding their underlying biology of metastasis. Our group has identified a disseminated neoplastic cell population characterized by co-expression of immune and melanoma proteins, circulating hybrid cells (hybrids), in patients with uveal melanoma. Compared to circulating tumor cells, which lack expression of immune proteins, hybrids are detected at an increased prevalence in peripheral blood </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-01T20:36:45.415Z</modification><creation>2025-05-18T13:26:44.772Z</creation></dates><accession>S-EPMC11264923</accession><cross_references><pubmed>39030653</pubmed><doi>10.1186/s40364-024-00609-6</doi></cross_references></HashMap>