<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE169139" accession="SRP311189">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP311189</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA715435</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE169139</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Modulation of  PSF binding property at RNA level by small molecule treatment in prostate cancer</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Prostate cancer is the most common cancer in men and androgen receptor (AR) downstream signalings promote prostate cancer cell proliferation. PSF is a RNA binding protein which is involved in AR signaling.To investigate the effect of samll molecule, No.10-3, on the RNA binding ability of PSF, we performed RNA immunoprecipitation (RIP) sequence analysis in AR positive prostate cancer cell line long term androgen deprivation (LTAD) cells to explore the differences of PSF function to associate with RNAs in prostate cancer cells. Overall design: RIP sequence analysis of PSF in prostate cancer cells</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE169139</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
