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The association between heat shock protein P2/P2 genotype with Egyptian hepatocellular carcinoma patients
Polymorphism of heat shock protein 70 (HSP70) at position 1267 may influence its expression. Many studies showed the importance of this polymorphism in developing cancers and some autoimmune diseases. In this study, we investigated the association of this polymorphism with the risk of hepatocellular...
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Published in: | Comparative clinical pathology 2013-11, Vol.22 (6), p.1183-1188 |
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description | Polymorphism of heat shock protein 70 (HSP70) at position 1267 may influence its expression. Many studies showed the importance of this polymorphism in developing cancers and some autoimmune diseases. In this study, we investigated the association of this polymorphism with the risk of hepatocellular carcinoma (HCC) in Egyptian patients. The study included 40 cases with HCC and 20 healthy age- and sex-matched subjects as control. The cases included 31 males (77.5 %) and 9 females (22.5 %). Their ages ranged from 42 to 70 years. HSPA1B 1267 was investigated using polymerase chain reaction with restriction fragment length polymorphism cutting with PstI enzyme. The two allelic forms were designated as the P1 allele and P2 allele. Among the HCC group, 14 patients (35 %) had P2/P2 genotype, 15 patients (37.5 %) had P1/P2 genotype, and 11 patients (27.5 %) had P1/P1 genotype. The frequencies of the HSPA1B P2/P2 genotype and the HSPA1B P2 allele in HCC patients were higher than in controls (each
p
= 0.0001). The risk for developing HCC in the homozygous HSPA1B P2/P2 genotype was 2.8-fold higher than that in the heterozygous P1/P2 genotype. In conclusion, polymorphism of HSP70 at position 1267 may be a risk for HCC development in Egyptians. |
doi_str_mv | 10.1007/s00580-012-1547-x |
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p
= 0.0001). The risk for developing HCC in the homozygous HSPA1B P2/P2 genotype was 2.8-fold higher than that in the heterozygous P1/P2 genotype. In conclusion, polymorphism of HSP70 at position 1267 may be a risk for HCC development in Egyptians.</description><identifier>ISSN: 1618-5641</identifier><identifier>EISSN: 1618-565X</identifier><identifier>DOI: 10.1007/s00580-012-1547-x</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>Hematology ; Medicine ; Medicine & Public Health ; Oncology ; Original Article ; Pathology</subject><ispartof>Comparative clinical pathology, 2013-11, Vol.22 (6), p.1183-1188</ispartof><rights>Springer-Verlag London Limited 2012</rights><rights>Springer-Verlag London 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c231x-7f91a900f065a229b9035b52081db8970cafb87315cf162cc7f98e8ca86957eb3</citedby><cites>FETCH-LOGICAL-c231x-7f91a900f065a229b9035b52081db8970cafb87315cf162cc7f98e8ca86957eb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>ElGemei, Shahira S.</creatorcontrib><creatorcontrib>Shaheen, Noha M.</creatorcontrib><creatorcontrib>Abu Khalil, Reham Emad</creatorcontrib><title>The association between heat shock protein P2/P2 genotype with Egyptian hepatocellular carcinoma patients</title><title>Comparative clinical pathology</title><addtitle>Comp Clin Pathol</addtitle><description>Polymorphism of heat shock protein 70 (HSP70) at position 1267 may influence its expression. Many studies showed the importance of this polymorphism in developing cancers and some autoimmune diseases. In this study, we investigated the association of this polymorphism with the risk of hepatocellular carcinoma (HCC) in Egyptian patients. The study included 40 cases with HCC and 20 healthy age- and sex-matched subjects as control. The cases included 31 males (77.5 %) and 9 females (22.5 %). Their ages ranged from 42 to 70 years. HSPA1B 1267 was investigated using polymerase chain reaction with restriction fragment length polymorphism cutting with PstI enzyme. The two allelic forms were designated as the P1 allele and P2 allele. Among the HCC group, 14 patients (35 %) had P2/P2 genotype, 15 patients (37.5 %) had P1/P2 genotype, and 11 patients (27.5 %) had P1/P1 genotype. The frequencies of the HSPA1B P2/P2 genotype and the HSPA1B P2 allele in HCC patients were higher than in controls (each
p
= 0.0001). The risk for developing HCC in the homozygous HSPA1B P2/P2 genotype was 2.8-fold higher than that in the heterozygous P1/P2 genotype. In conclusion, polymorphism of HSP70 at position 1267 may be a risk for HCC development in Egyptians.</description><subject>Hematology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Pathology</subject><issn>1618-5641</issn><issn>1618-565X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWKs_wFvA89pMdrObPUqpH1CwhwreQjZmu6ltsiYpbf-9KSvixdMMw_PODA9Ct0DugZBqEghhnGQEaAasqLLDGRpBCTxjJXs__-0LuERXIawJAcbzfITMstNYhuCUkdE4ixsd91pb3GkZceic-sS9d1Ebixd0sqB4pa2Lx17jvYkdnq2OfTTyxPcyOqU3m91GeqykV8a6rcRpbLSN4RpdtHIT9M1PHaO3x9ly-pzNX59epg_zTNEcDlnV1iBrQlpSMklp3dQkZw2jhMNHw-uKKNk2vMqBqRZKqlQKcM2V5GXNKt3kY3Q37E1vf-10iGLtdt6mkwKKgtesrHidKBgo5V0IXrei92Yr_VEAESejYjAqklFxMioOKUOHTEisXWn_Z_O_oW8DZ3p-</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>ElGemei, Shahira S.</creator><creator>Shaheen, Noha M.</creator><creator>Abu Khalil, Reham Emad</creator><general>Springer London</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201311</creationdate><title>The association between heat shock protein P2/P2 genotype with Egyptian hepatocellular carcinoma patients</title><author>ElGemei, Shahira S. ; Shaheen, Noha M. ; Abu Khalil, Reham Emad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c231x-7f91a900f065a229b9035b52081db8970cafb87315cf162cc7f98e8ca86957eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Hematology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ElGemei, Shahira S.</creatorcontrib><creatorcontrib>Shaheen, Noha M.</creatorcontrib><creatorcontrib>Abu Khalil, Reham Emad</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Comparative clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ElGemei, Shahira S.</au><au>Shaheen, Noha M.</au><au>Abu Khalil, Reham Emad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The association between heat shock protein P2/P2 genotype with Egyptian hepatocellular carcinoma patients</atitle><jtitle>Comparative clinical pathology</jtitle><stitle>Comp Clin Pathol</stitle><date>2013-11</date><risdate>2013</risdate><volume>22</volume><issue>6</issue><spage>1183</spage><epage>1188</epage><pages>1183-1188</pages><issn>1618-5641</issn><eissn>1618-565X</eissn><abstract>Polymorphism of heat shock protein 70 (HSP70) at position 1267 may influence its expression. Many studies showed the importance of this polymorphism in developing cancers and some autoimmune diseases. In this study, we investigated the association of this polymorphism with the risk of hepatocellular carcinoma (HCC) in Egyptian patients. The study included 40 cases with HCC and 20 healthy age- and sex-matched subjects as control. The cases included 31 males (77.5 %) and 9 females (22.5 %). Their ages ranged from 42 to 70 years. HSPA1B 1267 was investigated using polymerase chain reaction with restriction fragment length polymorphism cutting with PstI enzyme. The two allelic forms were designated as the P1 allele and P2 allele. Among the HCC group, 14 patients (35 %) had P2/P2 genotype, 15 patients (37.5 %) had P1/P2 genotype, and 11 patients (27.5 %) had P1/P1 genotype. The frequencies of the HSPA1B P2/P2 genotype and the HSPA1B P2 allele in HCC patients were higher than in controls (each
p
= 0.0001). The risk for developing HCC in the homozygous HSPA1B P2/P2 genotype was 2.8-fold higher than that in the heterozygous P1/P2 genotype. In conclusion, polymorphism of HSP70 at position 1267 may be a risk for HCC development in Egyptians.</abstract><cop>London</cop><pub>Springer London</pub><doi>10.1007/s00580-012-1547-x</doi><tpages>6</tpages></addata></record> |
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title | The association between heat shock protein P2/P2 genotype with Egyptian hepatocellular carcinoma patients |
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