<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE255015" accession="SRP488023">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP488023</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA1073203</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE255015</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Transcriptomic changes following NR1D1 modulation in thyroid cancer cell lines</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Nuclear receptor subfamily 1 group D member 1 (NR1D1), also known as Rev-Erba, is a circadian clock component that functions as a transcriptional repressor which coordinates circadian rhythm and cell metabolism. Altered circadian clock characteristics have been shown in malignant thyroid neoplasms, and NR1D1 is one of the recurrence-associated genes in papillary thyroid cancer. We aimed to investigate the biological role of NR1D1 in thyroid cancer cells. Overall design: Human thyroid cancer cell lines 8505C and CAL-62 were transfected with either a siRNA against NR1D1 or a control siRNA, whereas TPC-1 and FTC-133 cells were transfected with either an NR1D1-overexpressing vector or an empty vector. Cellular RNA was subjected to RNA sequencing.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE255015</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>39359072</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
