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<Article>
<Journal>
				<PublisherName>West Asia Organization for Cancer Prevention (WAOCP), APOCP's West Asia Chapter.</PublisherName>
				<JournalTitle>Asian Pacific Journal of Cancer Prevention</JournalTitle>
				<Issn>1513-7368</Issn>
				<Volume>16</Volume>
				<Issue>6</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effects of TESTIN Gene Expression on Proliferation and Migration of the 5-8F Nasopharyngeal Carcinoma Cell Line</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>2555</FirstPage>
			<LastPage>2559</LastPage>
			<ELocationID EIdType="pii">30777</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>1970</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</History>
		<Abstract>Purpose: To investigate effects of the TESTIN (TES) gene on proliferation and migration of highly metastaticnasopharyngeal carcinoma cell line 5-8F and the related mechanisms. Materials and &lt;br/&gt;&lt;b&gt;Methods&lt;/b&gt;: The target geneof human nasopharyngeal carcinoma cell line 5-8F was amplified by PCR and cloned into the empty plasmidpEGFP-N1 to construct a eukaryotic expression vector pEGFP-N1-TES. This was then transfected into 5-8Fcells. MTT assays, flow cytometry and scratch wound tests were used to detect the proliferation and migrationof transfected 5-8F cells. &lt;br/&gt;&lt;b&gt;Results&lt;/b&gt;: A cell model with stable and high expression of TES gene was successfullyestablished. MTT assays showed that the OD value of 5-8F/TES cells was markedly lower than that of 5-8F/GFPcells and 5-8F cells (p&lt;0.05). Flow cytometry showed that the apoptosis rate of 5-8F/TES cells was prominentlyincreased compared with 5-8F/GFP cells and 5-8F cells (p&lt;0.05). In vitro scratch wound assays showed that,the width of the wound area of 5-8F/TES cells narrowed slightly, while the width of the wound area of 5-8F/GFP cells and 5-8F cells narrowed sharply, suggesting that the TES overexpression could inhibit the migrationability. &lt;br/&gt;&lt;b&gt;Conclusions&lt;/b&gt;: TES gene expression remarkably inhibits the proliferation of human nasopharyngealcarcinoma cell line 5-8F and reduces its migration in vitro. Thus, it may be a potential tumor suppressor genefor nasopharyngeal carcinoma.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">TESTIN gene</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nasopharyngeal carcinoma</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Proliferation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">migration</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_30777_f8cf79e7f00658273e7b802659165528.pdf</ArchiveCopySource>
</Article>
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