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<ArticleSet>
<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>14</Volume>
				<Issue>9</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>09</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>miR-10b Promotes Migration and Invasion in Nasopharyngeal Carcinoma Cells</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>5533</FirstPage>
			<LastPage>5537</LastPage>
			<ELocationID EIdType="pii">28153</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>MicroRNA-10b (miR-10b) has been reported to play an important role in some types of cancer, but the effectsand possible mechanisms of action of miR-10b in the metastasis of nasopharyngeal carcinoma cells (NPC) havenot been explored. The aim of the present study was to investigate the function of miR-10b in nasopharyngealcarcinoma and to determine the molecular mechanisms underlying its action. The MTT assay was used toassess proliferation of CNE-2Z cells. Wound healing and transwell migration assays were applied to assesscell migration and invasion, while and expression of E-cadherin and MMP-9 were detected using Western blotanalysis. Real-time PCR was employed to detect the expression of genes related to migration and invasion andthe 2-ΔΔCt method was used to calculate the degree of expression. MTT assay showed the expression of miR-10bto have no effect on the proliferation of NPC cell lines. The wound healing assay showed that miR-10b mimicspromoted the mobility and invasion of NPC cell lines. Inhibitors of miR-10b reduced the ability of NPC cell linesto migrate and invade. In addition, the expression of genes related to migration and invasion, such as E-cadherin,vimentin, and MMP-9, were confirmed to be different in the CNE-2Z NPC cell line transfected with miR-10bmimics and with miR-10b inhibitors. In the present study, miR-10b was found to upregulate the expression ofMMP-9 and knockdown of miR-10b was found to significantly downregulate the expression of E-cadherin. Onthe whole, these results showed that miR-10b plays an important role in the invasion and metastasis of NPCcells.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">miR-10b</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">NPC</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Invasion</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Metastasis</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_28153_69f92e7adec1c3efe0fbaefbee9a2294.pdf</ArchiveCopySource>
</Article>
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