<?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>>2019</year>
	    <month>>October-December</month>
	    <day></day>
    </pubdate>
    <volume>11</volume>
    <number>4</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>31908740</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>Effect of Sodium Butyrate on &lt;I&gt;LHX1&lt;/I&gt; mRNA Expression as a Transcription Factor of HDAC8 in Human Colorectal 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&gt;Background: LHX1 is an important transcription factor for the &lt;em&gt;HDAC8&lt;/em&gt; gene. The aim of this study was to investigate the effect of Sodium Butyrate (SB), as a histone deacetylase inhibitor, on the expression of &lt;em&gt;LHX1&lt;/em&gt; gene in colorectal cancer cell lines.&amp;nbsp;&lt;br /&gt;
Methods: HT-29 and HCT-116 cell lines were treated with 6.25 to 200 &lt;em&gt;mM&lt;/em&gt; concentrations of SB at 24, 48, and 72 &lt;em&gt;hr&lt;/em&gt;. The cytotoxicity effect on cell viability was evaluated by MTT assay. The 50% Inhibiting Concentration (IC&lt;sub&gt;50&lt;/sub&gt;) was determined graphically. Quantitative real-time PCR was performed to investigate the LHX1 mRNA expression level.&amp;nbsp;&lt;br /&gt;
Results: Our study revealed that SB inhibited the proliferation of these cell lines in a concentration and time-dependent manner. The IC&lt;sub&gt;50&lt;/sub&gt; values for HT-29 cell line were 65, 18.6, and 9.2 &lt;em&gt;mM&lt;/em&gt; after 24, 48, and 72&lt;em&gt; hr&lt;/em&gt; of treatment, respectively. The IC&lt;sub&gt;50&lt;/sub&gt; values for HCT-116 cell line were 35.5, 9.6, and 10 &lt;em&gt;mM &lt;/em&gt;after 24, 48, and 72 &lt;em&gt;hr &lt;/em&gt;of treatment, respectively. Furthermore, real-time PCR findings demonstrated that the LHX1 mRNA expression in treated HT-29 cell line significantly increased in comparison with untreated cells (p&amp;lt;0.05). However, in treated HCT-116 cell line, SB led to a significant decrease in the level of LHX1 mRNA (p&amp;lt;0.05), as compared to untreated cells.&amp;nbsp;&lt;br /&gt;
Conclusion: In this study, different effects of SB on LHX1 mRNA expression level were revealed in two distinct human colorectal cancer cell lines.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Cytokine, Interleukin-10, Kawasaki disease, Single nucleotide polymorphisms, Transforming growth factor-beta</keyword>
	<start_page>317</start_page>
	<end_page>324</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=10389</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/10389.pdf</pdf_url>
	<author_list><author><first_name>Mahsa</first_name><middle_name></middle_name><last_name>Ghiaghi</last_name><suffix></suffix><affiliation>Department of Genetics, Faculty of Advanced Science 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>21489</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Flora</first_name><middle_name></middle_name><last_name>Forouzesh</last_name><suffix></suffix><affiliation>Department of Genetics, Faculty of Advanced Science 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>10</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hamzeh</first_name><middle_name></middle_name><last_name>Rahimi</last_name><suffix></suffix><affiliation>Department of Molecular Medicine, Pasteur Institute of Iran, 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>11464</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

