Polymorphism of Apolipoprotein E (APOE) gene in head and neck cancer
One of the risk factors for head and neck cancer (HNC) is genetics. Apolipoprotein E (APOE) polymorphism is known for affecting antioxidant activity which counteracts free radicals triggering cancer pathogenesis. The primary goal is to assess any relationship between APOE polymorphism and HNC. The s...
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description | One of the risk factors for head and neck cancer (HNC) is genetics. Apolipoprotein E (APOE) polymorphism is known for affecting antioxidant activity which counteracts free radicals triggering cancer pathogenesis. The primary goal is to assess any relationship between APOE polymorphism and HNC. The study is a descriptive research using analytic laboratory. Samples were obtained from Oral Biology Laboratory Faculty of Dentistry, University of Indonesia. The DNA used for evaluation consisted of 50 samples from patients with head and neck cancer and 50 controls. Polymorphism was identified using PCR-RFLP technique. As the result of the research, there are 100% polymorphisms in HNC and control groups. Fisher test results for genotype shows p=0,356 where the cancer group were 50 individuals with heterozygotes, 76% of individuals with the genotype ɛ2 / ɛ3, while 24% of individuals with the ɛ3 / ɛ4 genotype. There was no individual with homozygous genotypes wild type ɛ3 / ɛ3. In the control group, 49 individuals gained heterozygotes and 1 individual had homozygous genotypes. 80% of the control individuals had the genotype ɛ2 / ɛ3, 18% had the ɛ3 / ɛ4 genotype, and 2% with the ɛ4 / ɛ4 gene. Genotype distribution does not match Hardy-Weinberg equilibrium because the p value was less than 0.05. In conclusion, there was a relationship between APOE polymorphism and HNC as a reverse causality but there was no significant difference between APOE polymorphism and HNC. |
doi_str_mv | 10.1063/1.5096758 |
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Apolipoprotein E (APOE) polymorphism is known for affecting antioxidant activity which counteracts free radicals triggering cancer pathogenesis. The primary goal is to assess any relationship between APOE polymorphism and HNC. The study is a descriptive research using analytic laboratory. Samples were obtained from Oral Biology Laboratory Faculty of Dentistry, University of Indonesia. The DNA used for evaluation consisted of 50 samples from patients with head and neck cancer and 50 controls. Polymorphism was identified using PCR-RFLP technique. As the result of the research, there are 100% polymorphisms in HNC and control groups. Fisher test results for genotype shows p=0,356 where the cancer group were 50 individuals with heterozygotes, 76% of individuals with the genotype ɛ2 / ɛ3, while 24% of individuals with the ɛ3 / ɛ4 genotype. There was no individual with homozygous genotypes wild type ɛ3 / ɛ3. In the control group, 49 individuals gained heterozygotes and 1 individual had homozygous genotypes. 80% of the control individuals had the genotype ɛ2 / ɛ3, 18% had the ɛ3 / ɛ4 genotype, and 2% with the ɛ4 / ɛ4 gene. Genotype distribution does not match Hardy-Weinberg equilibrium because the p value was less than 0.05. In conclusion, there was a relationship between APOE polymorphism and HNC as a reverse causality but there was no significant difference between APOE polymorphism and HNC.</description><identifier>ISSN: 0094-243X</identifier><identifier>EISSN: 1551-7616</identifier><identifier>DOI: 10.1063/1.5096758</identifier><identifier>CODEN: APCPCS</identifier><language>eng</language><publisher>Melville: American Institute of Physics</publisher><subject>Antioxidants ; Apolipoproteins ; Cancer ; Dentistry ; Deoxyribonucleic acid ; DNA ; Free radicals ; Genotype & phenotype ; Head ; Head & neck cancer ; Laboratories ; Pathogenesis ; Polymorphism ; Risk analysis</subject><ispartof>AIP conference proceedings, 2019, Vol.2092 (1)</ispartof><rights>Author(s)</rights><rights>2019 Author(s). Published by AIP Publishing.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://pubs.aip.org/acp/article-lookup/doi/10.1063/1.5096758$$EHTML$$P50$$Gscitation$$H</linktohtml><link.rule.ids>310,311,315,781,785,790,791,795,4513,23935,23936,25145,27929,27930,76389</link.rule.ids></links><search><contributor>Wulan, Praswasti PDK</contributor><contributor>Gozan, Misri</contributor><contributor>Dhelika, Radon</contributor><contributor>Astutiningsih, Sotya</contributor><contributor>Ramahdita, Ghiska</contributor><contributor>Kreshanti, Prasetyanugraheni</contributor><creatorcontrib>Eugene, Lius Putri Felicia</creatorcontrib><creatorcontrib>Gultom, Ferry Pergamus</creatorcontrib><creatorcontrib>Midoen, Yurnadi Hanafi</creatorcontrib><creatorcontrib>Suhartono, Antonius Winoto</creatorcontrib><creatorcontrib>Marchelina, Triana</creatorcontrib><creatorcontrib>Auerkari, Elza Ibrahim</creatorcontrib><title>Polymorphism of Apolipoprotein E (APOE) gene in head and neck cancer</title><title>AIP conference proceedings</title><description>One of the risk factors for head and neck cancer (HNC) is genetics. Apolipoprotein E (APOE) polymorphism is known for affecting antioxidant activity which counteracts free radicals triggering cancer pathogenesis. The primary goal is to assess any relationship between APOE polymorphism and HNC. The study is a descriptive research using analytic laboratory. Samples were obtained from Oral Biology Laboratory Faculty of Dentistry, University of Indonesia. The DNA used for evaluation consisted of 50 samples from patients with head and neck cancer and 50 controls. Polymorphism was identified using PCR-RFLP technique. As the result of the research, there are 100% polymorphisms in HNC and control groups. Fisher test results for genotype shows p=0,356 where the cancer group were 50 individuals with heterozygotes, 76% of individuals with the genotype ɛ2 / ɛ3, while 24% of individuals with the ɛ3 / ɛ4 genotype. There was no individual with homozygous genotypes wild type ɛ3 / ɛ3. In the control group, 49 individuals gained heterozygotes and 1 individual had homozygous genotypes. 80% of the control individuals had the genotype ɛ2 / ɛ3, 18% had the ɛ3 / ɛ4 genotype, and 2% with the ɛ4 / ɛ4 gene. Genotype distribution does not match Hardy-Weinberg equilibrium because the p value was less than 0.05. In conclusion, there was a relationship between APOE polymorphism and HNC as a reverse causality but there was no significant difference between APOE polymorphism and HNC.</description><subject>Antioxidants</subject><subject>Apolipoproteins</subject><subject>Cancer</subject><subject>Dentistry</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Free radicals</subject><subject>Genotype & phenotype</subject><subject>Head</subject><subject>Head & neck cancer</subject><subject>Laboratories</subject><subject>Pathogenesis</subject><subject>Polymorphism</subject><subject>Risk analysis</subject><issn>0094-243X</issn><issn>1551-7616</issn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2019</creationdate><recordtype>conference_proceeding</recordtype><recordid>eNp9kEtLAzEUhYMoWKsL_0HAjQpT834sSx0fUGgXCu5CmsnYqW0SM1Oh_94pLbhzdQ-Xj3MOB4BrjEYYCfqARxxpIbk6AQPMOS6kwOIUDBDSrCCMfpyDi7ZdIUS0lGoAHudxvdvEnJZNu4GxhuMU102KKcfONwGW8HY8n5V38NMHD_vH0tsK2lDB4N0XdDY4ny_BWW3Xrb863iF4fyrfJi_FdPb8OhlPi0Q47QoiqwVRXGjklGCSKMoYklRKWjNWYeU4qoRVTkpL9nqhlagdV4xI7rRd0CG4Ofj27b63vu3MKm5z6CMNIYj3nkijnro_UK1rOts1MZiUm43NO4OR2a9ksDmu9B_8E_MfaFJV018SLmUm</recordid><startdate>20190409</startdate><enddate>20190409</enddate><creator>Eugene, Lius Putri Felicia</creator><creator>Gultom, Ferry Pergamus</creator><creator>Midoen, Yurnadi Hanafi</creator><creator>Suhartono, Antonius Winoto</creator><creator>Marchelina, Triana</creator><creator>Auerkari, Elza Ibrahim</creator><general>American Institute of Physics</general><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20190409</creationdate><title>Polymorphism of Apolipoprotein E (APOE) gene in head and neck cancer</title><author>Eugene, Lius Putri Felicia ; Gultom, Ferry Pergamus ; Midoen, Yurnadi Hanafi ; Suhartono, Antonius Winoto ; Marchelina, Triana ; Auerkari, Elza Ibrahim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p253t-27db285690c864728344073773f44d18c50d6a8c77a2c50db986fc584275c9ab3</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antioxidants</topic><topic>Apolipoproteins</topic><topic>Cancer</topic><topic>Dentistry</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Free radicals</topic><topic>Genotype & phenotype</topic><topic>Head</topic><topic>Head & neck cancer</topic><topic>Laboratories</topic><topic>Pathogenesis</topic><topic>Polymorphism</topic><topic>Risk analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eugene, Lius Putri Felicia</creatorcontrib><creatorcontrib>Gultom, Ferry Pergamus</creatorcontrib><creatorcontrib>Midoen, Yurnadi Hanafi</creatorcontrib><creatorcontrib>Suhartono, Antonius Winoto</creatorcontrib><creatorcontrib>Marchelina, Triana</creatorcontrib><creatorcontrib>Auerkari, Elza Ibrahim</creatorcontrib><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eugene, Lius Putri Felicia</au><au>Gultom, Ferry Pergamus</au><au>Midoen, Yurnadi Hanafi</au><au>Suhartono, Antonius Winoto</au><au>Marchelina, Triana</au><au>Auerkari, Elza Ibrahim</au><au>Wulan, Praswasti PDK</au><au>Gozan, Misri</au><au>Dhelika, Radon</au><au>Astutiningsih, Sotya</au><au>Ramahdita, Ghiska</au><au>Kreshanti, Prasetyanugraheni</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>Polymorphism of Apolipoprotein E (APOE) gene in head and neck cancer</atitle><btitle>AIP conference proceedings</btitle><date>2019-04-09</date><risdate>2019</risdate><volume>2092</volume><issue>1</issue><issn>0094-243X</issn><eissn>1551-7616</eissn><coden>APCPCS</coden><abstract>One of the risk factors for head and neck cancer (HNC) is genetics. Apolipoprotein E (APOE) polymorphism is known for affecting antioxidant activity which counteracts free radicals triggering cancer pathogenesis. The primary goal is to assess any relationship between APOE polymorphism and HNC. The study is a descriptive research using analytic laboratory. Samples were obtained from Oral Biology Laboratory Faculty of Dentistry, University of Indonesia. The DNA used for evaluation consisted of 50 samples from patients with head and neck cancer and 50 controls. Polymorphism was identified using PCR-RFLP technique. As the result of the research, there are 100% polymorphisms in HNC and control groups. Fisher test results for genotype shows p=0,356 where the cancer group were 50 individuals with heterozygotes, 76% of individuals with the genotype ɛ2 / ɛ3, while 24% of individuals with the ɛ3 / ɛ4 genotype. There was no individual with homozygous genotypes wild type ɛ3 / ɛ3. In the control group, 49 individuals gained heterozygotes and 1 individual had homozygous genotypes. 80% of the control individuals had the genotype ɛ2 / ɛ3, 18% had the ɛ3 / ɛ4 genotype, and 2% with the ɛ4 / ɛ4 gene. Genotype distribution does not match Hardy-Weinberg equilibrium because the p value was less than 0.05. In conclusion, there was a relationship between APOE polymorphism and HNC as a reverse causality but there was no significant difference between APOE polymorphism and HNC.</abstract><cop>Melville</cop><pub>American Institute of Physics</pub><doi>10.1063/1.5096758</doi><tpages>7</tpages></addata></record> |
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subjects | Antioxidants Apolipoproteins Cancer Dentistry Deoxyribonucleic acid DNA Free radicals Genotype & phenotype Head Head & neck cancer Laboratories Pathogenesis Polymorphism Risk analysis |
title | Polymorphism of Apolipoprotein E (APOE) gene in head and neck cancer |
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