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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>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2018</Year>
					<Month>02</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Impact of Cyclin D1 and Heterogeneous Nuclear Ribonucleoprotein-K (HnRNP-K) on Urinary Bladder Carcinogenesis</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>513</FirstPage>
			<LastPage>519</LastPage>
			<ELocationID EIdType="pii">57182</ELocationID>
			
<ELocationID EIdType="doi">10.22034/APJCP.2018.19.2.513</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Tarek </FirstName>
					<LastName>Aboushousha</LastName>
<Affiliation>Pathology Departments,Theodor Bilharz Research Institute, Cairo, Egypt.</Affiliation>
<Identifier Source="ORCID">0000-0002-6686-2442</Identifier>

</Author>
<Author>
					<FirstName>Olfat </FirstName>
					<LastName>Hammam</LastName>
<Affiliation>Pathology Departments,Theodor Bilharz Research Institute, Cairo, Egypt.</Affiliation>

</Author>
<Author>
					<FirstName>Noha </FirstName>
					<LastName>Helal</LastName>
<Affiliation>Pathology Departments,Theodor Bilharz Research Institute, Cairo, Egypt.</Affiliation>
<Identifier Source="ORCID">0000000304738857</Identifier>

</Author>
<Author>
					<FirstName>Samir </FirstName>
					<LastName>El Dahshan</LastName>
<Affiliation>Urology Departments, Theodor Bilharz Research Institute, Cairo, Egypt.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2017</Year>
					<Month>10</Month>
					<Day>03</Day>
				</PubDate>
			</History>
		<Abstract>Objective: This study aimed to investigate the expression of cyclin D1 and hnRNP-K in relation to the pathological&lt;br /&gt;findings in bladder cancer including the type, grade, muscle invasion and bilharzial association. Methods: We studied&lt;br /&gt;the immunoexpression; as regard the percentage, intensity and score of both cyclin D1 and hnRNP-K in different bladder&lt;br /&gt;lesions including 10 cases of cystitis; 10 cases of carcinoma insitu (CIS), 20 cases of Squamous cell carcinoma (SCC)&lt;br /&gt;and 66 cases of urothelial carcinoma (UC). Results: High expression of cyclin D1 was found in UC compared to other&lt;br /&gt;groups (p&lt;0.001) and in UC with low grade, non-muscle invasive and papillary tumors compared to their counterparts&lt;br /&gt;(p&lt;0.05, hnRNP-K expression was found in SCC compared to other groups (p &lt;0.001) and in UC with high grade, muscle invasive&lt;br /&gt;and non-papillary tumors compared to their counterparts (p&lt;0.001each). Bilharzial-associated UC showed higher&lt;br /&gt;expression of hnRNP-K percent (p&lt;0.05) compared to non-bilharzial cases. Conclusion: This study elucidated a possible&lt;br /&gt;contribution of cyclin D1 and hnRNP-K expression in the initiation and progression of urinary bladder carcinoma,&lt;br /&gt;so, both of them can be used in predicting progression of urinary bladder carcinoma and to differentiate between UC&lt;br /&gt;and SCC in high grade tumors. The possible role of both markers in immunotherapy deserves supplementary studies.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">bladder cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">bilharziasis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cyclin D1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">hnRNP-K</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">immunohistochemistry</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_57182_1534ae6ce334389b33d761a3c5d01444.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
