<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Biomedical Journal</title>
<title_fa>مجله بیومدیکال ایران</title_fa>
<short_title>IBJ</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ibj.pasteur.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1028-852X</journal_id_issn>
<journal_id_issn_online>2008-823X</journal_id_issn_online>
<journal_id_pii>-</journal_id_pii>
<journal_id_doi>10.61882/ibj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>-</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>-</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1403</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2025</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>29</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_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Expression Pattern Study of miR-200a and XIAP Gene in the Non-small Cell Lung Cancer Patients’ blood</title>
	<subject_fa>Molecular Genetics &amp; Genomics</subject_fa>
	<subject>Molecular Genetics &amp; Genomics</subject>
	<content_type_fa>مقاله کامل</content_type_fa>
	<content_type>Full Length/Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;span style=&quot;font-family:Times New Roman;&quot;&gt;&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt;Background:&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt; In non-small cell lung cancer (NSCLC), miR-200a plays a significant role in apoptosis. One of the genes involved in this pathway is &lt;i&gt;XIAP&lt;/i&gt;, which has been shown anti-apoptotic activity. Research has indicated a significant association between miR-200a and &lt;span style=&quot;color:black&quot;&gt;the&lt;i&gt; XIAP&lt;/i&gt; gene in this pathway. The present study investigated the expression profiles of &lt;/span&gt;miR-200a &lt;span style=&quot;color:black&quot;&gt;and the &lt;/span&gt;&lt;i&gt;&lt;span style=&quot;color:black&quot;&gt;XIAP&lt;/span&gt;&lt;/i&gt;&lt;span style=&quot;color:black&quot;&gt; gene in NSCLC patients compared to normal individuals, as well as cancer cells compared to normal and apoptosis-inducing conditions.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt;Methods:&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt; &lt;span style=&quot;color:black&quot;&gt;In this study, 40 blood specimens were collected from NSCLC patients and 40 from healthy individuals. After isolating plasma and peripheral blood mononuclear cells from these samples, we analyzed &lt;/span&gt;&lt;span style=&quot;color:black&quot;&gt;the miR-200a and &lt;i&gt;XIAP&lt;/i&gt; gene expression levels using real-time PCR. &lt;/span&gt;Subsequently, normal and lung cancer cells were treated with paclitaxel as a model of apoptosis. The antiproliferative effects and induction of apoptosis were then evaluated using the MTT and flow cytometry assays, respectively. Finally, the expression patterns of miR-200a and the &lt;i&gt;&lt;span style=&quot;color:black&quot;&gt;XIAP&lt;/span&gt;&lt;/i&gt;&lt;span style=&quot;color:black&quot;&gt; gene &lt;/span&gt;were investigated through a real-time PCR method.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;span style=&quot;font-size:11pt&quot;&gt;&lt;span style=&quot;line-height:normal&quot;&gt;&lt;b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt;Results:&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt; Results indicated that the miR-200a expression level was lower in NSCLC patients than in healthy ones, while the expression level of &lt;i&gt;XIAP&lt;/i&gt; gene increased in the NSCLC Patients&amp;rsquo; blood. The MTT and flow cytometry results demonstrated a decreased proliferation and increased apoptosis rates in two lung line cells (A549 and MRC5) treated with paclitaxel. &lt;i&gt;XIAP &lt;/i&gt;expression level also decreased in A549 cells treated with paclitaxel compared to untreated A549 cells.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;br&gt;
&lt;b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt;Conclusion:&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:10.5pt&quot;&gt;&lt;span style=&quot;line-height:115%&quot;&gt; MiR-200a may be associated with the &lt;i&gt;XIAP&lt;/i&gt; gene expression and the induction of the apoptosis pathway in NSCLC. &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Apoptosis, Gene expression, MicroRNAs, Non-small cell lung carcinoma</keyword>
	<start_page>49</start_page>
	<end_page>56</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-3567-3&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Tara</first_name>
	<middle_name></middle_name>
	<last_name>Fereydouni</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>tarafereydouni1995@gmail.com</email>
	<code></code>
	<orcid>0009-0007-0398-5262</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biology, Alborz Campus, University of Tehran, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seyed Jalal</first_name>
	<middle_name></middle_name>
	<last_name>Zargar</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>zargar@ut.ac.ir</email>
	<code></code>
	<orcid>0000-0001-8157-3588</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Cell and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Sharareh</first_name>
	<middle_name></middle_name>
	<last_name>Seifi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>sh_seifi@yahoo.com</email>
	<code></code>
	<orcid>0000-0002-1340-0949</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Adult Hematology and Oncology, School of Medicine,  Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mojgan</first_name>
	<middle_name></middle_name>
	<last_name>Sheikhpour</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>m_sheikhpour@pasteur.ac.ir</email>
	<code></code>
	<orcid>0000-0002-1927-6555</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
