<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE88757" accession="SRP091559">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP091559</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA348471</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE88757</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Identification of miR-100 and miR-125b targets by AGO2 RIP-seq and RNA-seq after ectopic expression of miR-100 or miR-125b and evaluation of the TGFb expression signature in PANC-1 cells by RNA-seq</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>To identify targets post-transcriptionally regulated by miR-100 and miR-125b, we have performed AGO2 RIP-seq and RNA-seq following overexpression of the two miRNAs in PANC-1 cells.  In addition, we have carried out RNA-seq following TGFb stimulus to evaluate changes in gene expression driven by TGFb. Overall design: For AGO2 RIP-seq and RNA-seq PANC-1 cells were transfected with precursor miRNA mimics for miR-100, miR-125b and negative control (0.5nM) for 24h. The experiment was performedin two biological replicates. For evaluation of changes in gene expression driven by TGFb PANC-1 cells were treated with TGFb (5nM) or vehicle control for 72h. Three biological replicates for each condition were used for expression analysis.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE88757</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>29748571</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA348461</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
