<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2025</year>
	    <month>>Jan-Mar</month>
	    <day></day>
    </pubdate>
    <volume>17</volume>
    <number>1</number>
    <publish_type>online</publish_type>
    <publish_edition>1</publish_edition>
    <article_type>fulltext</article_type>
    <articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>40094094</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Comparison of Anticancer Effects between Platinum Levetiracetam and Platinum  Azidothymidine through the Expression of Biomarker Genes on Cancer Cell Lines</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&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;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Bcl-2, Levetiracetam, miRNAs, Telomerase, Zidovudine</keyword>
	<start_page>24</start_page>
	<end_page>30</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60599</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60599.pdf</pdf_url>
	<author_list><author><first_name>Abdolreza</first_name><middle_name></middle_name><last_name>Sabokrouh</last_name><suffix></suffix><affiliation></affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>793</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nasim</first_name><middle_name></middle_name><last_name>Ghaffari</last_name><suffix></suffix><affiliation>Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92268</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Zahra</first_name><middle_name></middle_name><last_name>Karimi Tafreshi </last_name><suffix></suffix><affiliation>Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92269</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Freshteh</first_name><middle_name></middle_name><last_name>Atabi</last_name><suffix></suffix><affiliation>Department of Biochemistry and Biophysics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92270</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Zohreh</first_name><middle_name></middle_name><last_name>Sharifi</last_name><suffix></suffix><affiliation>Blood Transfusion Research Center, High institute for Research and Education in Transfusion Medicine, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>640</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Seyyed Khalil</first_name><middle_name></middle_name><last_name>Shokouhi Mostafavi </last_name><suffix></suffix><affiliation>Department of Microbiology, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>92324</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

