<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sui Y</submitter><funding>Kobe University</funding><funding>Japan Society for the Promotion of Science</funding><pagination>444-457</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10140238</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>58(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Amino acid transporters play an important role in supplying nutrition to cells and are associated with cell proliferation. L-type amino acid transporter 1 (LAT1) is highly expressed in many types of cancers and promotes tumor growth; however, how LAT1 affects tumor development is not fully understood.&lt;h4>Methods&lt;/h4>To investigate the role of LAT1 in intestinal tumorigenesis, mice carrying LAT1 floxed alleles that also expressed Cre recombinase from the promoter of gene encoding Villin were crossed to an Apc&lt;sup>Min/+&lt;/sup> background (LAT1&lt;sup>fl/fl&lt;/sup>; vil-cre; Apc&lt;sup>Min/+&lt;/sup>), which were subject to analysis; organoids derived from those mice were also analyzed.&lt;h4>Results&lt;/h4>This study showed that LAT1 was constitutively expressed in normal crypt base cells, </pubmed_abstract><journal>Journal of gastroenterology</journal><pubmed_title>LAT1 expression influences Paneth cell number and tumor development in Apc&lt;sup>Min/+&lt;/sup> mice.</pubmed_title><pmcid>PMC10140238</pmcid><funding_grant_id>20H04123</funding_grant_id><funding_grant_id>19K08421</funding_grant_id><pubmed_authors>Ku Y</pubmed_authors><pubmed_authors>Sasaki K</pubmed_authors><pubmed_authors>Kong L</pubmed_authors><pubmed_authors>Kinoshita M</pubmed_authors><pubmed_authors>Yoshida R</pubmed_authors><pubmed_authors>Ito Y</pubmed_authors><pubmed_authors>Sui Y</pubmed_authors><pubmed_authors>Kotani T</pubmed_authors><pubmed_authors>Shinohara M</pubmed_authors><pubmed_authors>Kanai Y</pubmed_authors><pubmed_authors>Tokunaga E</pubmed_authors><pubmed_authors>Tian Z</pubmed_authors><pubmed_authors>Matozaki T</pubmed_authors><pubmed_authors>Ohgaki R</pubmed_authors><pubmed_authors>Watanabe D</pubmed_authors><pubmed_authors>Hoshi N</pubmed_authors><pubmed_authors>Kodama Y</pubmed_authors><pubmed_authors>Miyazaki H</pubmed_authors><pubmed_authors>Okamoto N</pubmed_authors><pubmed_authors>Ooi M</pubmed_authors><pubmed_authors>Zen Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>LAT1 expression influences Paneth cell number and tumor development in Apc&lt;sup>Min/+&lt;/sup> mice.</name><description>&lt;h4>Background&lt;/h4>Amino acid transporters play an important role in supplying nutrition to cells and are associated with cell proliferation. L-type amino acid transporter 1 (LAT1) is highly expressed in many types of cancers and promotes tumor growth; however, how LAT1 affects tumor development is not fully understood.&lt;h4>Methods&lt;/h4>To investigate the role of LAT1 in intestinal tumorigenesis, mice carrying LAT1 floxed alleles that also expressed Cre recombinase from the promoter of gene encoding Villin were crossed to an Apc&lt;sup>Min/+&lt;/sup> background (LAT1&lt;sup>fl/fl&lt;/sup>; vil-cre; Apc&lt;sup>Min/+&lt;/sup>), which were subject to analysis; organoids derived from those mice were also analyzed.&lt;h4>Results&lt;/h4>This study showed that LAT1 was constitutively expressed in normal crypt base cells, </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-05-18T13:25:52.279Z</modification><creation>2025-02-19T02:57:11.214Z</creation></dates><accession>S-EPMC10140238</accession><cross_references><pubmed>36739585</pubmed><doi>10.1007/s00535-023-01960-5</doi></cross_references></HashMap>