<?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>>2023</year>
	    <month>>April-June</month>
	    <day></day>
    </pubdate>
    <volume>15</volume>
    <number>2</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>37034893</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>Study of DACH1 Expression and its Epigenetic Regulators as Possible Breast Cancer-Related Biomarkers</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; Breast carcinogenesis involves both genetic and epigenetic changes. DNA methylation, as well as micro-RNA regulations, are the significant epigenetic phenomena dysregulated in breast cancer&lt;strong&gt;.&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;Herein, the expression of&amp;nbsp;&lt;em&gt;DACH1&lt;/em&gt;&amp;nbsp;as a tumor suppressor gene and its promoter methylation status was analyzed in breast cancer tumors. Also, the expression of three micro RNAs (miR-217, miR-6807-3p, and miR-552), which had been previously reported to target &lt;em&gt;DACH1&lt;/em&gt;, was assessed.&amp;nbsp; &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;The SYBR green-based Real-Time reverse transcription-PCR was used to determine&amp;nbsp;&lt;em&gt;DACH1&lt;/em&gt;&amp;nbsp;and micro-RNAs (miR-217, miR-6807-3p, and miR-552) expression in 120 ductal breast cancer tumors compared with standard control. Also, the promoter methylation pattern of&amp;nbsp;&lt;em&gt;DACH1&lt;/em&gt;&amp;nbsp;was investigated using the &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;Methylation-specific PCR&lt;em&gt; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;technique. &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;em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;DACH1&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&amp;nbsp;expression was significantly down-regulated in breast tumors (p&amp;lt; 0.05). About 33.5% of tumors showed&amp;nbsp;&lt;em&gt;DACH1&lt;/em&gt;&amp;nbsp;promoter hyper-methylation. The studied micro-RNAs, expression was negatively correlated with &lt;em&gt;DACH1&lt;/em&gt; expression. The highest expressions of miRNAs and higher&amp;nbsp;&lt;em&gt;DACH1&lt;/em&gt;&amp;nbsp;promoter methylation were observed in advanced cancer situations. The Kaplan-Meier survival curves indicated that the overall survival was significantly poor in higher miRNAs and lower &lt;em&gt;DACH1&lt;/em&gt; expression in breast cancer patients (p&amp;lt;0.002).&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;

&lt;p&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;em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt; DACH1&lt;/span&gt;&lt;/em&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;&amp;nbsp;down-regulation may be associated with a poor breast cancer prognosis. The&amp;nbsp;&lt;em&gt;DACH1&lt;/em&gt; down-regulation may be due to epigenetic regulations such as promoter methylation, especially in triple-negative cases. Other factors, such as micro-RNAs (miR-217, miR-6807-3p, and miR-552), may also have an &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;impact. The elevated expression of &lt;/span&gt;&lt;span style=&quot;font-size:10.0pt&quot;&gt;miR-217, miR-6807-3p, and miR-552, maybe candidates as possible poor prognostic biomarkers in breast cancer management for further consideration.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Breast cancer, DACH1, Methylation, miR-217, miR-552, miR-6807-3p</keyword>
	<start_page>108</start_page>
	<end_page>117</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=60537</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/60537.pdf</pdf_url>
	<author_list><author><first_name>Mohammad Hossein</first_name><middle_name></middle_name><last_name>Nasirpour</last_name><suffix></suffix><affiliation>Department of Medical Genetics, Institute of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), , 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>92029</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Mahdieh</first_name><middle_name></middle_name><last_name>Salimi</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>741</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Faezeh</first_name><middle_name></middle_name><last_name>Majidi</last_name><suffix></suffix><affiliation>Department of Biology, Science and Research Branch, 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>92030</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Zarrin</first_name><middle_name></middle_name><last_name>Minuchehr</last_name><suffix></suffix><affiliation>Institute of Industrial and Environmental Biotechnology (IIEB), National Institute of Genetic Engineering and Biotechnology (NIGEB), 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>494</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hossein</first_name><middle_name></middle_name><last_name>Mozdarani</last_name><suffix></suffix><affiliation>Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares 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>321</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

