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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>8</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>08</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Association between RASSF1A Ala133Ser Polymorphism and Cancer Susceptibility: A Meta-Analysis Involving 8,892 Subjects</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>3691</FirstPage>
			<LastPage>3698</LastPage>
			<ELocationID EIdType="pii">29141</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; Published studies on the association between the Ras Association Domain Family 1 isoform A(RASSF1A) Ala133Ser polymorphism and cancer susceptibility have yielded conflicting results. Thus, a metaanalysiswas here performed to assess the possible association. Materials and &lt;br/&gt;&lt;b&gt;Methods&lt;/b&gt;: All eligible case-controlstudies published up to November 2013 on the association between RASSF1A Ala133Ser polymorphism and cancersusceptibility were identified by searching PubMed, Web of Science, Science Direct and hand search. Bothfixedeffectand random-effect models were used to calculate pooled odds ratios (ORs) with 95% confidence intervals(CIs) by using the Comprehensive Meta-Analysis software version 2.2. &lt;br/&gt;&lt;b&gt;Results&lt;/b&gt;: A total of 10 studies including4,572 cancer cases and 4,320 controls were included in the meta-analysis. Overall, significantly increased cancerrisk was associated with the variant Ser133 when all studies were pooled (Ser vs Ala: OR=1.51, 95% CI=1.08-2.12, Pheterogeneity≤0.001; Ser/Ser+Ala/Ser vs Ala/Ala: OR=1.55, 95% CI=1.08-2.22, Pheterogeneity≤0.001). Moreover,in subgroup analyses by cancer types, a significant association between RASSF1A Ala133Ser polymorphismand lung cancer risk was found (Ser vs Ala: OR=2.27, 95% CI=1.29-4.02, Pheterogeneity=0.61; Ser/Ser+Ala/Ser vs Ala/Ala: OR=2.42, 95% CI=1.33-4.42, Pheterogeneity=0.75). In addition, in subgroup analyses by ethnicity, itwas found that the RASSF1A Ala133Ser polymorphism was associated with overall cancer risk in Asians (Servs Ala: OR=1.37, 95% CI=1.06-1.77, Pheterogeneity=0.06) and Caucasians (Ser/Ser+Ala/Ser vs Ala/Ala: OR=2.21,95% CI=1.01-4.82, Pheterogeneity≤0.001). &lt;br/&gt;&lt;b&gt;Conclusions&lt;/b&gt;: This meta-analysis suggests, for the first time, that RASSF1AAla133Ser polymorphism may contribute to cancer susceptibility, especially for lung cancer. Besides, additionalwell-designed studies with larger sample size focusing on different ethnicities and cancer types are needed toconfirm these findings.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">RASSF1A</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">RASSF1A Ala133Ser polymorphism</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cancer susceptibility</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Meta-analysis</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_29141_895568f824017f4a78e695f5b04c4b41.pdf</ArchiveCopySource>
</Article>
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