<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Urbanska K</submitter><funding>NCI NIH HHS</funding><pagination>1130-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4596767</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(10)</volume><pubmed_abstract>Adoptive transfer of T cells engineered to express chimeric immunoreceptors is an effective strategy to treat hematologic cancers; however, the use of this type of therapy for solid cancers, such as ovarian cancer, remains challenging because a safe and effective immunotherapeutic target has not yet been identified. Here, we constructed and evaluated a novel redirected T-cell-based immunotherapy targeting human follicle-stimulating hormone receptor (FSHR), a highly conserved molecule in vertebrate animals with expression limited to gonadal tissues, ovarian cancer, and cancer-associated vasculature. Receptor ligand-based anti-FSHR immunoreceptors were constructed that contained small binding fragments from the ligand for FSHR, FSH, fused to T-cell transmembrane and T-cell signaling domains.</pubmed_abstract><journal>Cancer immunology research</journal><pubmed_title>Follicle-Stimulating Hormone Receptor as a Target in the Redirected T-cell Therapy for Cancer.</pubmed_title><pmcid>PMC4596767</pmcid><funding_grant_id>R01 CA168900</funding_grant_id><funding_grant_id>R01-CA168900</funding_grant_id><pubmed_authors>Stashwick C</pubmed_authors><pubmed_authors>Urbanska K</pubmed_authors><pubmed_authors>Poussin M</pubmed_authors><pubmed_authors>Powell DJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Follicle-Stimulating Hormone Receptor as a Target in the Redirected T-cell Therapy for Cancer.</name><description>Adoptive transfer of T cells engineered to express chimeric immunoreceptors is an effective strategy to treat hematologic cancers; however, the use of this type of therapy for solid cancers, such as ovarian cancer, remains challenging because a safe and effective immunotherapeutic target has not yet been identified. Here, we constructed and evaluated a novel redirected T-cell-based immunotherapy targeting human follicle-stimulating hormone receptor (FSHR), a highly conserved molecule in vertebrate animals with expression limited to gonadal tissues, ovarian cancer, and cancer-associated vasculature. Receptor ligand-based anti-FSHR immunoreceptors were constructed that contained small binding fragments from the ligand for FSHR, FSH, fused to T-cell transmembrane and T-cell signaling domains.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Oct</publication><modification>2025-04-19T14:59:14.656Z</modification><creation>2019-03-27T01:59:40Z</creation></dates><accession>S-EPMC4596767</accession><cross_references><pubmed>26112923</pubmed><doi>10.1158/2326-6066.cir-15-0047</doi><doi>10.1158/2326-6066.CIR-15-0047</doi></cross_references></HashMap>