﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Pharmaceutical Sciences</JournalTitle>
      <Issn>1735-403X</Issn>
      <Volume>28</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2022</Year>
        <Month>07</Month>
        <DAY>27</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>A Review of the Biological Roles of MiR-4800; A Novel Tumor Biomarker with Therapeutic Potential</ArticleTitle>
    <FirstPage>376</FirstPage>
    <LastPage>382</LastPage>
    <ELocationID EIdType="doi">10.34172/PS.2021.48</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Monireh</FirstName>
        <LastName>Khordadmehr</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-4472-3847</Identifier>
      </Author>
      <Author>
        <FirstName>Reyhaneh</FirstName>
        <LastName>Matin</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-7523-8978</Identifier>
      </Author>
      <Author>
        <FirstName>Behzad</FirstName>
        <LastName>Baradaran</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8642-6795</Identifier>
      </Author>
      <Author>
        <FirstName>Amir</FirstName>
        <LastName>Baghbanzadeh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-1261-3213</Identifier>
      </Author>
      <Author>
        <FirstName>Farinaz</FirstName>
        <LastName>Jigari-Asl</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-5710-970X</Identifier>
      </Author>
      <Author>
        <FirstName>Farzad</FirstName>
        <LastName>Katiraee</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8634-4378</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/PS.2021.48</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>08</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <Abstract>MicroRNAs (miRNAs) are known as a group of short noncoding ribonucleic acids (ncRNAs). Mainly, they can manage gene expression at the posttranscriptional level in the essential biological and physiological functions. Significantly, more than 50% of the discovered miRNAs genes are placed in cancer‐related genomic regions, which can act as oncomiR or oncosuppressor. In this regard, growing evidence recently demonstrated the deregulation of miR-4800 in human cancers and non-cancerous diseases. However, little information is available on the biological roles of miR-4800 in cancer initiation, development, and progression. Here, we reviewed the targeting sites and biogenesis functions of the miR‐4800 family in physiological and pathological processes like human cancers, particularly with a particular focusing on the validated specific targets.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Cancer Progression</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Microrna</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Physiological Function</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Therapeutic Aspect</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>