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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Hauptverfasser: Eugene, Lius Putri Felicia, Gultom, Ferry Pergamus, Midoen, Yurnadi Hanafi, Suhartono, Antonius Winoto, Marchelina, Triana, Auerkari, Elza Ibrahim
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container_volume 2092
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Gultom, Ferry Pergamus
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Marchelina, Triana
Auerkari, Elza Ibrahim
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.
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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. 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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. 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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.</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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source American Institute of Physics (AIP) Journals
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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