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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>15</Volume>
				<Issue>14</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>IL-12 Regulates B7-H1 Expression in Ovarian Cancerassociated Macrophages by Effects on NF-κB Signalling</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>5767</FirstPage>
			<LastPage>5772</LastPage>
			<ELocationID EIdType="pii">29494</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>Background and Aim: B7-H1, a co-inhibitory molecule of the B7 family, is found aberrantly expressed inovarian cancer cells and infiltrating macrophage/dendritic-like cells, and plays a critical role in immune evasionby ovarian cancer. IL-12, an inducer of Th1 cell development, exerts immunomodulatory effects on ovariancancer. However, whether IL-12 regulates B7-H1 expression in human ovarian cancer associated-macrophageshas not been clarified. Therefore, we investigated the effects of IL-12 on the expression of B7-H1 in ovariancancer-associated macrophages and possible mechanisms. &lt;br/&gt;&lt;b&gt;Methods&lt;/b&gt;: PMA induced THP-1-derived macrophagesor human monocyte-derived macrophages were treated with recombinant IL-12 (rIL-12) or infected withadenovirus carrying human IL-12 gene (Ad-IL-12-GFP) for 24 h, then cocultured with the SKOV3 ovariancancer cell line for another 24 h. Macrophages were collected for real-time PCR and Western blot to detect theexpression of B7-H1, and activation of the NF-κB signaling pathway. Moreover, supernatants were collected toassay for IL-12, IFN-γ and IL-10 by ELISA. In addition, monocyte-derived macrophages treated with IFN-γ werecocultured with SKOV3 and determined for the expression of B7-H1. Furthermore, the expression of B7-H1 inmonocyte-derived macrophages was also evaluated after blocking NF-κB signaling. &lt;br/&gt;&lt;b&gt;Results&lt;/b&gt;: The expression ofB7-H1 was significantly upregulated in monocyte-derived macrophages treated with rIL-12 or Ad-IL-12-GFPcompared with the control groups (p&lt;0.05), accompanied by a remarkable upregulation of IFN-γ (p&lt;0.05), amarked downregulation of IL-10 (p&lt;0.05) and activation of NF-κB signaling. However, the upregulation of B7-H1 was inhibited by blocking the NF-κB signaling pathway (p&lt;0.05). Expression of B7-H1 was also increased(p&lt;0.05) in monocyte-derived macrophages treated with IFN-γ and cocultured with SKOV3. By contrast, theexpression of B7-H1 in THP-1-derived macrophages was significantly decreased when treated in the same wayas monocyte-derived macrophages (p&lt;0.05), and IL-10 was also significantly decreased but IFN-γ was almostabsent. &lt;br/&gt;&lt;b&gt;Conclusions&lt;/b&gt;: IL-12 upregulates the expression of B7-H1 in monocyte-derived macrophages, which ispossible though inducing the secretion of IFN-γ and further activating the NF-κB signal pathway. However,IL-12 downregulates the expression of B7-H1 in THP-1-derived macrophages, associated with a lack of IFN-γand inhibition of expression of IL-10.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Ovarian Cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">B7-H1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">IL-12</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">IFN-γ</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">NF-κB signaling pathway</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_29494_832b898964d7fdf8b572d01db5280dca.pdf</ArchiveCopySource>
</Article>
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