<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE106696" accession="SRP124641">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP124641</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA417696</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE106696</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>RNA-seq analysis of gene expression in scramble and GPR126 knockdown colon cancer cells (HT-29)</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Purpose: Identify genes regulated by GPR126 in colon cancer cells by RNA-seq analysis Methods: Use shRNAs to knock down GPR126 in HT-29 cells, total RNAs from scramble group (NC) and GPR126 knockdown group (Sh1) were subjected to RNA-sequencing. Results: Around 700 transcriptomes were up-regulated in GPR126 knockdown HT-29 cells, and 14000 transcriptomes were down-regulated in GPR126 knockdown HT-29 cells.GPR126 mainly regualtes genes from DNA synthesis and cell cycle-related pathways. Conclusions: Our study firstly showed the function of GPR126 regulating colon cancer cell proliferation by targeting genes invovled in DNA synthesis and cell cycle-related pathways. Overall design: RNA interference in colon cancer cell line HT-29, knock down GPR126 expression, and conduct gene expression profiling by RNA-seq. Two groups, one sample from each group.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE106696</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
