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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>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Plumbagin from Plumbago Zeylanica L Induces Apoptosis in Human Non-small Cell Lung Cancer Cell Lines through NFkB Inactivation</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>2325</FirstPage>
			<LastPage>2331</LastPage>
			<ELocationID EIdType="pii">27628</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>&lt;br /&gt;&lt;strong&gt;Objective&lt;/strong&gt;: To detect effects of plumbagin on proliferation and apoptosis in non-small cell lung cancer celllines, and investigate the underlying mechanisms. Materials and &lt;br /&gt;&lt;strong&gt;Methods&lt;/strong&gt;: Human non-small cell lung cancercell lines A549, H292 and H460 were treated with various concentrations of plumbagin. Cell proliferationrates was determined using both cell counting kit-8 (CCK-8) and clonogenic assays. Apoptosis was detected byannexin V/propidium iodide double-labeled flow cytometry and TUNEL assay. The levels of reactive oxygenspecies (ROS) were detected by flow cytometry. Activity of NF-kB was examined by electrophoretic mobilityshift assay (EMSA) and luciferase reporter assay. Western blotting was used to assess the expression of bothNF-kB regulated apoptotic-related gene and activation of p65 and IkBk. &lt;br /&gt;&lt;strong&gt;Results&lt;/strong&gt;: Plumbagin dose-dependentlyinhibited proliferation of the lung cancer cells. The IC50 values of plumbagin in A549, H292, and H460 cells were10.3 μmol/L, 7.3 μmol/L, and 6.1 μmol/L for 12 hours, respectively. The compound concentration-dependentlyinduced apoptosis of the three cell lines. Treatment with plumbagin increased the intracellular level of ROS, andinhibited the activation of NK-kB. In addition to inhibition of NF-kB/p65 nuclear translocation, the compoundalso suppressed the degradation of IkBk. ROS scavenger NAC highly reversed the effect of plumbagin onapoptosis and inactivation of NK-kB in H460 cell line. Treatment with plumbagin also increased the activity ofcaspase-9 and caspase-3, downregulated the expression of Bcl-2, upregulated the expression of Bax, Bak, andCytC. &lt;br /&gt;&lt;strong&gt;Conclusions&lt;/strong&gt;: Plumbagin inhibits cell growth and induces apoptosis in human lung cancer cells throughan NF-kB-regulated mitochondrial-mediated pathway, involving activation of ROS.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Plumbagin</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">NSCLC</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apoptosis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">NF-KB</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">reactive oxygen species</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">mitochondrial pathway</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">caspase</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_27628_776c5c82e00648a4a5fd344fc4dfaa9c.pdf</ArchiveCopySource>
</Article>
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