<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE218575" accession="SRP409276">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP409276</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA904345</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE218575</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Transcriptomic analysis of Nintedanib, Alpelisib and Nintedanib;Alpelisib treated bladder tumors</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Nintedanib is a potent anti-fibrotic angio-kinase inhibitor, which has shown clinical efficacy in combination with chemotherapy in locally advanced muscle invasive BC patients. Nintedanib inhibits Fibroblast Growth Factor receptors (FGFRs), validated targets in patients with BC harboring FGFR3/2 genetic alterations. Here, we aimed at studying its mechanisms of action to understand therapy their combination (n=4). Reads were mapped separately against the human and mouse genomes to differentiate tumor vs. stromal expression changes Overall design: In order to gain insight into the mechanisms underlying Nintedanib and Alpelisib synergism in vivo, we tested the effects of Nintedanib, Alpelisib (BYL719) and their combination on  ScaBER cells xenografts. We performed RNA sequencing of tumors treated for 14 days with either either vehicle (n=4), Nintedanib  (n=4), Alpelisib (n=4), or their combination (n=4). Reads were mapped separately against the human and mouse genomes to differentiate tumor vs. stromal expression changes</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE218575</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>36805958</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
