<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE216610" accession="SRP404608">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP404608</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA894501</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE216610</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>P-TEFb promotes cell survival upon p53 activation by suppressing intrinsic apoptosis pathway</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>We used RNA sequencing to deciphere a molecular basis for the synthethic lethality of non-genotoxic p53 activation and P-TEFb inhibition. Overall design: We treated HCT116 cell line in biological triplicates with DMSO, Nutlin-3a (10 uM), NVP-2 (20 nM), and Nutlin-3a (10 uM) together with NVP-2 (20 nM) for 8 hours.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE216610</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>36727434</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
