<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Kanehira N</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4&gt;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</pubmed_abstract><journal>Journal of translational medicine</journal><pagination>1387</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12683832</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tumor marker-guided precision BNCT for CA19-9-positive cancers: a new paradigm in molecularly targeted chemoradiation therapy.</pubmed_title><pmcid>PMC12683832</pmcid><pubmed_authors>Shigeyasu K</pubmed_authors><pubmed_authors>Suzuki M</pubmed_authors><pubmed_authors>Fujita T</pubmed_authors><pubmed_authors>Fujimoto T</pubmed_authors><pubmed_authors>Gotoh K</pubmed_authors><pubmed_authors>Sakurai Y</pubmed_authors><pubmed_authors>Takarada T</pubmed_authors><pubmed_authors>Kamei K</pubmed_authors><pubmed_authors>Tajima T</pubmed_authors><pubmed_authors>Osone T</pubmed_authors><pubmed_authors>Michiue H</pubmed_authors><pubmed_authors>Nagahisa N</pubmed_authors><pubmed_authors>Kanehira N</pubmed_authors><pubmed_authors>Fujiwara T</pubmed_authors><pubmed_authors>Kondo N</pubmed_authors><pubmed_authors>Morihara A</pubmed_authors><pubmed_authors>Takaguchi Y</pubmed_authors><pubmed_authors>Teraishi F</pubmed_authors><pubmed_authors>Kitamatsu M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tumor marker-guided precision BNCT for CA19-9-positive cancers: a new paradigm in molecularly targeted chemoradiation therapy.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4&gt;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</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-07T03:13:46.642Z</modification><creation>2026-06-07T03:07:13.341Z</creation></dates><accession>S-EPMC12683832</accession><cross_references><pubmed>41361823</pubmed><doi>10.1186/s12967-025-07349-7</doi></cross_references></HashMap>