<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE186196" accession="SRP342259">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP342259</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA772940</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE186196</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Genetic screens discover proteases as synthetic lethal partners of PI3K inhibition in breast cancer cells</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>The RNA-Seq analysed the changes in protease gene expression upon short-term PI3K inhibition in three breast cancer cell lines. Overall design: MCF7, MDA-MB-231 and PyB6-313 breast cancer cells were seeded, 16 h later RNA was isolated (T0; Medium control). Remaining plates were treated with the PI3K inhibitor BKM (NVP-BKM-120 [Buparlisib], CT-BKM120; Chemitek) at EC50 (200 nM [MCF7], 1300 nM [MDA-MB-231], 1500 nM [PyB6-313]), or the same dilution of DMSO (solvent control). After 3 h of treatment, RNA was isolated. Conditions were prepared in triplicates.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE186196</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>35673573</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
