<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>2</title>
<title_fa>1</title_fa>
<short_title>3</short_title>
<subject>Literature &amp; Humanities</subject>
<web_url>http://idai.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>9</journal_id_issn>
<journal_id_issn_online>10</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>7</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1390</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2012</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>4</volume>
<number>4</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa>Synthesized Pheophorbide a-mediated photodynamic therapy induced apoptosis and autophagy in human oral squamous carcinoma cells</title_fa>
	<title></title>
	<subject_fa>پاتولوزی دهان، فک و صورت</subject_fa>
	<subject>Oral and Maxillofacial Pathology</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa>&lt;p&gt; &lt;strong&gt;Background: &lt;/strong&gt; Pheophorbide a (Pa) is a chlorine-based photosensitizer derived from an ethnopharmacological herb, and our group recently synthesized Pa by the removal of a magnesium ion and a phytyl group from chlorophyll-a. In this study, the effect of photodynamic therapy (PDT) with synthesized Pa was examined in a human oral squamous cell carcinoma (OSCC) cells. &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Methods: &lt;/strong&gt; Cells were treated with PDT with Pa, and reactive oxygen species (ROS) and mitochondrial membrane potential [ΔΨ (m)] were examined. Apoptosis was measured using annexin V staining and immunoblot. Autophagy was characterized by the increase in LC3B-II and the formation of autophagosome and acidic vesicular organelles (AVOs). &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Results:&lt;/strong&gt;  Pa-PDT inhibited the proliferation of OSCC cells in a dose-dependent manner. Pa-PDT increased the number of apoptotic cells by inactivating ERK pathway. Pa-PDT also induced autophagy in OSCC cells evidenced by the increased levels of LC3 type II expression and the accumulation of AVOs. The inhibition of autophagy enhanced Pa-PDT-mediated cytotoxicity through an increase in necrosis. &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Conclusions:&lt;/strong&gt;  These results suggest that synthesized Pa-PDT exerts anti-tumor effects by inducing apoptosis and autophagy and provide novel evidence that Pa-PDT induces autophagy, and autophagy inhibition enhances Pa-PDT-mediated necrosis in OSCC cells. &lt;/p&gt;&lt;hr&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt; &lt;strong&gt;Source: &lt;/strong&gt;Journal of Oral Pathology &amp; Medicine&lt;/p&gt;&lt;p&gt;&lt;a href=&quot;http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0714.2012.01187.x/abstract&quot; target=&quot;_blank&quot;&gt;&lt;font color=&quot;#0000ff&quot;&gt; Full Text&lt;/font&gt;&lt;/a&gt;&lt;/p&gt;</abstract_fa>
	<abstract></abstract>
	<keyword_fa>apoptosis;autophagy;necrosis;oral sqaumous cell carcinoma;synthesized Pa-PDT</keyword_fa>
	<keyword></keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://idai.ir/browse.php?a_code=A-10-32-2211&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Mee Young</first_name>
	<middle_name></middle_name>
	<last_name>Ahn</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>ahnsg@chosun.ac.kr</email>
	<code>100319475328460010421</code>
	<orcid>100319475328460010421</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Pathology, Research Center for Oral disease Regulation of the Aged, School of Dentistry, Chosun University, Gwangju, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Hyo-Eun</first_name>
	<middle_name></middle_name>
	<last_name>Yoon</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></email>
	<code>100319475328460010422</code>
	<orcid>100319475328460010422</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pathology, Research Center for Oral disease Regulation of the Aged, School of Dentistry, Chosun University, Gwangju, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seong-Min</first_name>
	<middle_name></middle_name>
	<last_name>Kwon</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></email>
	<code>100319475328460010423</code>
	<orcid>100319475328460010423</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pathology, Research Center for Oral disease Regulation of the Aged, School of Dentistry, Chosun University, Gwangju, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Jun</first_name>
	<middle_name></middle_name>
	<last_name>Lee</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></email>
	<code>100319475328460010424</code>
	<orcid>100319475328460010424</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Oral &amp; Maxillofacial Surgery, College of Dentistry, Daejeon Dental Hospital, Wonkwang Bone Regeneration Institute, Wonkwang University, Daejeon, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Seung-Ki</first_name>
	<middle_name></middle_name>
	<last_name>Min</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></email>
	<code>100319475328460010425</code>
	<orcid>100319475328460010425</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Oral &amp; Maxillofacial Surgery, College of Dentistry, Daejeon Dental Hospital, Wonkwang Bone Regeneration Institute, Wonkwang University, Daejeon, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Yung-Chul</first_name>
	<middle_name></middle_name>
	<last_name>Kim</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></email>
	<code>100319475328460010426</code>
	<orcid>100319475328460010426</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Life Science, Gwangju Institute of Science and Technology, Gwangju, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Hoon</first_name>
	<middle_name></middle_name>
	<last_name>Yoon</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></email>
	<code>100319475328460010427</code>
	<orcid>100319475328460010427</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Oral &amp; Maxillofacial Pathology, College of Dentistry, Daejeon Dental Hospital, Wonkwang Bone Regeneration Institute, Wonkwang University, Daejeon, Korea</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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