<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Karalis JD</submitter><funding>burroughs wellcome fund</funding><funding>mark foundation for cancer research</funding><funding>dedman family scholarship</funding><funding>NCI NIH HHS</funding><funding>national cancer institute</funding><pagination>116</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8900296</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Lenvatinib is a multitargeted tyrosine kinase inhibitor that is being tested in combination with immune checkpoint inhibitors to treat advanced gastric cancer; however, little data exists regarding the efficacy of lenvatinib monotherapy. Patient-derived xenografts (PDX) are established by engrafting human tumors into immunodeficient mice. The generation of PDXs may be hampered by growth of lymphomas. In this study, we compared the use of mice with different degrees of immunodeficiency to establish PDXs from a diverse cohort of Western gastric cancer patients. We then tested the efficacy of lenvatinib in this system.&lt;h4>Methods&lt;/h4>PDXs were established by implanting gastric cancer tissue into NOD.Cg-Prkdc&lt;sup>scid&lt;/sup>Il2rg&lt;sup>tm1Wjl&lt;/sup>/SzJ (NSG) or Foxn1&lt;sup>nu&lt;/su</pubmed_abstract><journal>Journal of translational medicine</journal><pubmed_title>Lenvatinib inhibits the growth of gastric cancer patient-derived xenografts generated from a heterogeneous population.</pubmed_title><pmcid>PMC8900296</pmcid><funding_grant_id>R01 CA251928</funding_grant_id><funding_grant_id>K08 CA222611</funding_grant_id><funding_grant_id>1018897</funding_grant_id><funding_grant_id>P30 CA142543</funding_grant_id><pubmed_authors>Hammer STG</pubmed_authors><pubmed_authors>Polanco PM</pubmed_authors><pubmed_authors>Suarez J</pubmed_authors><pubmed_authors>Castro-Dubon EC</pubmed_authors><pubmed_authors>Reznik SI</pubmed_authors><pubmed_authors>Mansour JC</pubmed_authors><pubmed_authors>Nassour I</pubmed_authors><pubmed_authors>Zhu H</pubmed_authors><pubmed_authors>Wang SC</pubmed_authors><pubmed_authors>Xiao S</pubmed_authors><pubmed_authors>Hong C</pubmed_authors><pubmed_authors>Zhu M</pubmed_authors><pubmed_authors>Agrawal D</pubmed_authors><pubmed_authors>Ju MR</pubmed_authors><pubmed_authors>Hwang TH</pubmed_authors><pubmed_authors>Karalis JD</pubmed_authors><pubmed_authors>Zeh HJ</pubmed_authors><pubmed_authors>Porembka MR</pubmed_authors><pubmed_authors>Yoon LY</pubmed_authors><pubmed_authors>Yopp AC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lenvatinib inhibits the growth of gastric cancer patient-derived xenografts generated from a heterogeneous population.</name><description>&lt;h4>Background&lt;/h4>Lenvatinib is a multitargeted tyrosine kinase inhibitor that is being tested in combination with immune checkpoint inhibitors to treat advanced gastric cancer; however, little data exists regarding the efficacy of lenvatinib monotherapy. Patient-derived xenografts (PDX) are established by engrafting human tumors into immunodeficient mice. The generation of PDXs may be hampered by growth of lymphomas. In this study, we compared the use of mice with different degrees of immunodeficiency to establish PDXs from a diverse cohort of Western gastric cancer patients. We then tested the efficacy of lenvatinib in this system.&lt;h4>Methods&lt;/h4>PDXs were established by implanting gastric cancer tissue into NOD.Cg-Prkdc&lt;sup>scid&lt;/sup>Il2rg&lt;sup>tm1Wjl&lt;/sup>/SzJ (NSG) or Foxn1&lt;sup>nu&lt;/su</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-04-12T15:03:19.673Z</modification><creation>2025-04-04T13:21:59.39Z</creation></dates><accession>S-EPMC8900296</accession><cross_references><pubmed>35255940</pubmed><doi>10.1186/s12967-022-03317-7</doi></cross_references></HashMap>