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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>15</Volume>
				<Issue>23</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A Sphingosine Kinase-1 Inhibitor, SKI-II, Induces Growth Inhibition and Apoptosis in Human Gastric Cancer Cells</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>10381</FirstPage>
			<LastPage>10385</LastPage>
			<ELocationID EIdType="pii">30277</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>SKI-II has been reported as an inhibitor of sphingosine kinase 1 and has been extensively used to prove theinvolvement of sphingosine kinase and sphingosine-1-phosphate (Sphk1) in cellular processes. In the currentstudy, we investigated the effects of SKI-II and its potential mechanisms in human gastric cancer SGC7901cells. After treatment with SKI-II, cell growth, cell cycle distribution, apoptosis, expression of Sphk1, NF-κB,Bcl-2, Bax and p27 were assessed by MTT assay, flow cytometry, electron microscopy, immunocytochemistryand Western-blot assay, respectively. Our results showed that SKI-II markedly inhibited SGC7901 cell survivalin a dose-dependent manner, reduced cell proliferation with accumulation of cells in the G0/G1 phase andinduced apoptosis in the tumor cells. Furthermore, Western blotting and immunocytochemistry showed that theexpression of p27 and Bax was increased significantly, but the expression of NF-κB, Bcl-2 and Sphk1 decreasedby different degrees. These results indicate that SKI-II induced cell growth arrest and apoptosis. The increasedapoptotic sensitivity of SGC7901 was correlated with NF-κB or Bcl-2/Bax activation.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Sphingosine kinase 1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">SKI-II</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Proliferation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apoptosis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">SGC7901 gastric cancer cells</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_30277_fae2e6ac1413f161bbaa9f1216d0c68c.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
