<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE180200" accession="SRP328548">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP328548</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA747013</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE180200</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>QPCTL deletion results in a rewiring of the tumor microenvironment [bulk RNA-seq]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>bulk RNA sequencing performed on the FACS sorted CD45-negative cells from QPCTL-proficient and -deficient TMEs; and, base-line comparison of lymphoid organs from QPCTL-KO and QPCTL-WT animals Overall design: The effects of QPCTL-deficiency were assessed in this study. To this end, a QPCTL-KO mouse strain was used. Mice homozygous for the QPCTL-KO allele or wild-type littermates were innoculated with either QPCTL-KO or QPCTL B16F10 tumor cells, respectively. After 14 days tumors were harvested, single cell suspensions were made and live CD45-negative cells were isolated by FACS, after which cells were processed for RNA sequencing. For baseline samples, whole organs were harvested from mice, snapfrozen and used for mRNA isolations.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE180200</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>35309731</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA747011</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
