<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<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>12</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Tumor Necrosis Factor-α Gene Polymorphisms and Risk of Oral Cancer: Evidence from a Meta-analysis</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>7243</FirstPage>
			<LastPage>7249</LastPage>
			<ELocationID EIdType="pii">28439</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>Numerous studies have been conducted regarding association between TNF-α and oral cancer risk, but theresults remain controversial. The present meta-analysis is performed to acquire a more precise estimation ofrelationships. Databases of Pubmed, the Cochrane library and the China National Knowledge Internet (CNKI)were retrieved until August 10, 2013. Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) werecalculated with fixed- or random-effect models. The heterogeneity assumption was assessed by I-squared test.Among the eight included case-control studies, all were focused on TNF-α-308G&gt;A and four also concernedthe TNF-α-238G&gt;A polymorphism. It was found that oral cancer risk were significant decreased with theTNF-α-308G&gt;A polymorphism in the additive genetic model (GG vs. AA, OR=0.19, 95% CI: [0.04, 1.00],P=0.05, I2=68.9%) and the dominant genetic model (GG+GA vs. AA, OR=0.22, 95% CI: [0.06, 0.82], P=0.03,I2=52.4%); however, no significant association was observed in allele contrast (G vs. A, OR=0.70, 95% CI: [0.23,2.16], P=0.54, I2=95.9%) and recessive genetic models (GG vs. GA+AA, OR=0.72, 95% CI: [0.33, 1.57], P=0.41,I2=93.1%). For the TNF-α-238G&gt;A polymorphism, significant associations with oral cancer risk were found inthe allele contrast (G vs. A, OR=2.75, 95% CI: [1.25, 6.04], P=0.01, I2=0.0%) and recessive genetic models (GGvs. GA+AA, OR=2.23, 95%CI: [1.18, 4.23], P=0.01, I2=0.0%). Conclusively, this meta-analysis indicates thatTNF-α polymorphisms may contribute to the risk of oral cancer. Allele G and the GG+GA genotype of TNF-α-308G&gt;A may decrease the risk of oral cancer, while allele G and the GG genotype of TNF-α-238G&gt;A may causean increase.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Tumor Necrosis Factor-α</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">oral cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Meta-analysis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Polymorphism</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_28439_bbdb116c7633659ccdeeda50ba746f9c.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
