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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>21</Volume>
				<Issue>11</Issue>
				<PubDate PubStatus="epublish">
					<Year>2020</Year>
					<Month>11</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>DNA Methyltransferases as Potential Biomarkers for HCV Related Hepatocellular Carcinoma</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>3357</FirstPage>
			<LastPage>3363</LastPage>
			<ELocationID EIdType="pii">89359</ELocationID>
			
<ELocationID EIdType="doi">10.31557/APJCP.2020.21.11.3357</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mona M</FirstName>
					<LastName>Hassouna</LastName>
<Affiliation>Department of Clinical and Chemical Pathology, National Liver Institute, Menoufia University, Shebeen El-Kom, Egypt.</Affiliation>

</Author>
<Author>
					<FirstName>Mary </FirstName>
					<LastName>Naguib</LastName>
<Affiliation>Department of Clinical and Chemical Pathology, National Liver Institute, Menoufia University, Shebeen El-Kom, Egypt.</Affiliation>

</Author>
<Author>
					<FirstName>Enas M</FirstName>
					<LastName>Radwan</LastName>
<Affiliation>Department of Clinical pathology, National Cancer Institute, Cairo University, Cairo, Egypt.</Affiliation>

</Author>
<Author>
					<FirstName>Mohamed </FirstName>
					<LastName>Abdel-Samiee</LastName>
<Affiliation>Hepatology and Gastroenterology, National Liver Institute, Clinical Pathology, Menoufia University, Shebeen El-Kom, Egypt.</Affiliation>
<Identifier Source="ORCID">0000 0002 8970 0286</Identifier>

</Author>
<Author>
					<FirstName>Suzanne </FirstName>
					<LastName>Estaphan</LastName>
<Affiliation>Department of Physiology, Faculty of Medicine, Cairo University, Cairo, Egypt.</Affiliation>

</Author>
<Author>
					<FirstName>Eman </FirstName>
					<LastName>Abdelsameea</LastName>
<Affiliation>Hepatology and Gastroenterology, National Liver Institute, Clinical Pathology, Menoufia University, Shebeen El-Kom, Egypt.</Affiliation>
<Identifier Source="ORCID">0000-0002-3225-7164</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2020</Year>
					<Month>08</Month>
					<Day>02</Day>
				</PubDate>
			</History>
		<Abstract>Background: Hepatocellular carcinoma (HCC) is a major health concern in many countries including Egypt. The alteration in DNA methylation that was observed in HCC patients suggests a possible role of DNA methyltransferases (DNMTs) in the disease pathogenesis in addition to potential role as a disease biomarker. Aim: To study the change in DNMTs expression in chronic HCV infected patients as potential non- invasive biomarker for diagnosis of hepatocellular carcinoma. Methods: 26 patients with HCC, 45 patients with liver cirrhosis, 20 chronic HCV patients and 20 apparently healthy individuals as a control group were enrolled in this study. Real-Time Quantitative Reverse Transcription PCR (qRT-PCR) was performed for all study participants. Results: A significant difference in DNMTs expression was observed among the studied groups. Receiver operating characteristics (ROC) curve analysis revealed that with a cutoff value of 3.16 for DNMT 3A expression, sensitivity and specificity were 80.8 and 95.6% respectively and area under curve (AUC) was 0.958, p &lt; 0.001 for discriminating hepatocellular carcinoma among post hepatitis C cirrhotic patients. Besides DNMT 3B relative expression cutoff value of 3.10 showed 84.6% sensitivity and 77.8% specificity and AUC was 0.888, p &lt; 0.001. On the other hand, cutoff value 0.65 for DNMT1 relative expression showed 92.3% sensitivity and 44.4% specificity and AUC was 0.72, p= 0.002. DNMT1, DNMT 3A and DNMT 3B have significant positive correlation with the level of AFP (p-value = 0.003, 0.004 and 0.008 respectively). The relative expression of DNMT3B was significantly correlated to focal lesion size (p-value = 0.015). High DNMTs expression was significantly associated with the presence of multiple focal lesions but not with the Child Pugh grade (p&gt; 0.05). Conclusion: The mRNA levels of DNMTs could be a potential biomarker for early detection of HCC development.&lt;br /&gt;  </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Hepatocellular carcinoma</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">DNA methlyltransferase</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Epigenetics</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">DNA Methylation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">HCV</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_89359_172548a58fabece0df75bd04edd8bf4e.pdf</ArchiveCopySource>
</Article>
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