Ontology highlight
ABSTRACT: Background
Boron neutron capture therapy (BNCT) is a molecularly targeted chemoradiation modality that relies on boron delivery agents such as p-borophenylalanine (BPA), which require LAT1 (L-type amino acid transporter 1) for tumor uptake. However, the limited efficacy of BPA in LAT1-low tumors restricts its therapeutic scope. To address this limitation, we developed a tumor marker-guided BNCT strategy targeting cancers overexpressing the clinically validated glycan biomarker CA19-9.Methods
We conducted transcriptomic analyses using The Cancer Genome Atlas (TCGA) datasets to identify LAT1-low cancers with high CA19-9 expression. These analyses revealed elevated expression of fucosyltransferase 3 (FUT3), which underlies CA19-9 biosynthesis, in pancreatic, biliary, and ovari
SUBMITTER: Kanehira N
PROVIDER: S-EPMC12683832 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature