<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE140708" accession="SRP230777">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP230777</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA590634</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE140708</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Mutual dependency between a lncRNA and NPM1 is crucial for tumor cell proliferation</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Silencing LETN or NPM1 in  hepatocellular carcinoma cells inhibited cell proliferation and resulted in identical phenotypes. RNA-seq further revealed that knock-down of lncRNA LETN and NPM1 resulted in similar shifts of the gene expression profiles. This lncRNA-protein axis therefore plays indispensable roles in highly proliferative cells including a multitude of cancer cells and human neuronal precursor cells. Here we provide processed raw counts files. Overall design: siLETN, siNPM1 and control (siNC) experiments with 2 replicates respectively.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE140708</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>33432115</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
