<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>52</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2023</Year>
        <Month>01</Month>
        <Day>30</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Differential Expression of lincRNA-ROR Spliced Transcript  Variants in Breast Cancer</title>
    <FirstPage>427</FirstPage>
    <LastPage>435</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mozhgan</FirstName>
        <LastName>Sadat Akhtar</LastName>
        <affiliation locale="en_US">Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Akram</FirstName>
        <LastName>Gholipour</LastName>
        <affiliation locale="en_US">Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahrokh</FirstName>
        <LastName>Bagheri Moghadam</LastName>
        <affiliation locale="en_US">Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Maziar</FirstName>
        <LastName>Oveisee</LastName>
        <affiliation locale="en_US">1.	School of Medicine, Bam University of Medical Sciences, Bam, Iran 2. Clinical Research Center, Pastor Educational Hospital, Bam University of Medical Sciences, Bam, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Javad</FirstName>
        <LastName>Mowla</LastName>
        <affiliation locale="en_US">Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahshid</FirstName>
        <LastName>Malakootian</LastName>
        <affiliation locale="en_US">Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2022</Year>
        <Month>05</Month>
        <Day>27</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2022</Year>
        <Month>11</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: We investigated the expression pattern of a human stem cell-specific, large intergenic noncoding RNA (lincRNA) regulator of reprogramming (lincRNA-ROR) and its spliced transcript variants in breast tumors. Breast cancer is the leading cause of cancer mortality in women; therefore, finding a reliable diagnostic tumor marker, based on the molecular profile of tumor cells, is warranted.
&#xD;

Methods: qRT-PCR was used to investigate the expression alteration of a specific stem cell-related lincRNA and its spliced transcript variants in breast tumors which provided by the Iran National Tumor Bank (2014-2016). Suitability of lincRNA-ROR and expression alterations of its spliced transcript variants as breast tumor biomarkers were examined by ROC curve analysis.
&#xD;

Results: Expression was significantly upregulated in lincRNA-ROR variants 1 (NR-048536) and 4 (AB844432) and downregulated in variant 3 (AB844431), with expression levels failing to distinguish between breast tumor types, grades, and malignancy stages. Whereas ROC curve analysis gave good scores to the expressions of variants 1 (AUC=0.7675, P=0.003) and 3 (AUC=0.9383, P=0.00173), suggesting their suitability as potential breast tumor biomarkers, it gave an AUC score of 0.6033 for lincRNA-ROR spliced variant 4 (P=0.4118), denoting its unsuitability as a breast cancer biomarker.
&#xD;

Conclusion: Aberrant expressions of lincRNA-ROR spliced transcript variants could serve as reliable biomarkers with potential usefulness in breast cancer diagnosis. However, further research should elucidate the role and tissue expression of lincRNA-ROR spliced transcript variants in various cancers.
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&#xA0;</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/28877</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/28877/7868</pdf_url>
  </Article>
</Articles>
