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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>14</Volume>
				<Issue>11</Issue>
				<PubDate PubStatus="epublish">
					<Year>2013</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Association Between the XRCC3 Thr241Met Polymorphism and Cervical Cancer Risk: a Meta-analysis</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>6703</FirstPage>
			<LastPage>6707</LastPage>
			<ELocationID EIdType="pii">28172</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;b&gt;Background:&lt;/b&gt; Numerous epidemiological studies have been conducted to evaluate the association betweenvariants of the DNA repair gene XRCC3 and cancer risk. Here we focused on one XRCC3 polymorphism anddevelopment of cervical cancer, performing a meta-analysis. &lt;br/&gt;&lt;b&gt;Methods&lt;/b&gt;: The pooled association between theXRCC3 Thr241Met polymorphism and cervical cancer risk was assessed by odds ratios (ORs) and their 95%confidence intervals (95%CIs). &lt;br/&gt;&lt;b&gt;Results&lt;/b&gt;: A total of 5 case-control studies met the inclusion criteria. The pooledORs for the total included studies showed no association among homozygotes TT vs. CC: OR=1.93, 95%CI=0.68-5.49, P=0.22; dominant model TT+TC vs. CC: OR=1.37, 95%CI=0.90-2.06, P=0.14; and recessive model TT vs.TC+CC: OR=1.76, 95%CI=0.68-4.55, P=0.25, but might be a slight risk factor for cervical cancer in heterozygotecontrast TT vs. CT: OR= 1.33, 95%CI=1.04-1.71, P=0.02. In subgroup analysis, significant associations werefound for Asians under all genetic models. &lt;br/&gt;&lt;b&gt;Conclusions&lt;/b&gt;: Our meta-analysis suggested the XRCC3 Thr241Metpolymorphism might not act as a cervical cancer risk factor overall. However, in subgroup analysis, a significantassociation was found in Asians under all genetic models. The association should be studied with a larger, stratifiedpopulation, especially for Asians.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">cervical cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">XRCC3</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Polymorphism</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Meta-analysis</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_28172_cc64264ec0fd1264aaf2c3ce8a6fd38a.pdf</ArchiveCopySource>
</Article>
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