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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Avicenna J Med Biotech</journal-id>
      <journal-id journal-id-type="publisher-id">arij002</journal-id>
      <journal-title-group>
        <journal-title>Avicenna Journal of Medical Biotechnology</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2008-2835</issn>
      <issn pub-type="epub">2008-4625</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">ajmb60599</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Comparison of Anticancer Effects between Platinum Levetiracetam and Platinum  Azidothymidine through the Expression of Biomarker Genes on Cancer Cell Lines</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Sabokrouh</surname><given-names>Abdolreza</given-names></name></contrib><aff>Department of Molecular Medicine &amp; Genetics, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Ghaffari</surname><given-names>Nasim</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Karimi Tafreshi </surname><given-names>Zahra</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Atabi</surname><given-names>Freshteh</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Sharifi</surname><given-names>Zohreh</given-names></name></contrib><aff>Department of Pharmaceutical Biotechnology, Faculty of Pharmacy and Biotechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Shokouhi Mostafavi </surname><given-names>Seyyed Khalil</given-names></name></contrib></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>17</volume>
      <issue>1</issue>
      <fpage>24</fpage>
      <lpage>30</lpage>
      <history>
        <date date-type="received">
          <day>14</day>
          <month>6</month>
          <year>2024</year>
        </date>
        <date date-type="accepted">
          <day>2</day>
          <month>10</month>
          <year>2024</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Background:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The utilization of biomarkers is a way to assess the efficacy of recently created anticancer drugs. MiRNAs, telomerase, and Bcl-2 are extensively utilized as biomarkers for this purpose. This study aims to evaluate the comparison of the newly synthesized platinum compounds such as Platinum Azidothymidine (Pt-AZT) with Platinum Levetiracetam (Pt-Lev) on HepG2 cancer cell lines &lt;em&gt;via&lt;/em&gt; the biomarkers. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methods:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; In this study, cells were divided into four groups: Group A (HDF cells) were the normal negative control group, group B were HepG2 untreated cancer cells, and groups C and D were treated cancer cells with Pt-AZT and Pt-Lev, respectively. After evaluating the LC&lt;sub&gt;50&lt;/sub&gt; for the drugs by MTT test, the relative gene expression of the biomarkers was determined by qPCR.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Results:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; The results showed a significant decrease for antiapoptotic genes including miRNA-21 (5.1&amp;plusmn;0.014), telomerase (0.56&amp;plusmn;0.48), Bcl-2 (0.41&amp;plusmn;0.276) in group D, whereas in group C was more than group D for miRNA-21 (6.0&amp;plusmn;0.141), telomerase (3.49&amp;plusmn;0.231), Bcl-2 (4.93&amp;plusmn;0.276) also there was a significant increase in miRNA-122 (33.97&amp;plusmn;0.04) in group D, whereas in group C was (28.36&amp;plusmn;0.007) and so lower than group D. Most of the investigated groups showed a significant difference (p&amp;lt;0.05). In addition, there were widespread apoptotic regions in Pt-Lev treatment compared to Pt-AZT. &lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Conclusion:&lt;/span&gt;&lt;/strong&gt; &lt;span style=&quot;font-size:10.0pt&quot;&gt;The advantages of using Pt-Lev were more powerful anticancer effects on biomarkers through inhibition of antiapoptotic and stimulation proapoptotic factors and also lower side effects and lower drug resistance than Pt-AZT; therefore, it can be considered a more effective anti-cancer therapy.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

      </p>
      </abstract>
    </article-meta>
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