Influence of IL-6, IL-8, and TGF-β1 gene polymorphisms on the risk of human papillomavirus-infection in women from Pernambuco, Brazil
Human papillomavirus (HPV) infections are strongly associated with the development of cervical intraepithelial neoplasias and invasive cervical cancer. Polymorphisms in cytokine-encoding genes and behavioural cofactors could play an important role in protecting an individual against viral infections...
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Published in | Memórias do Instituto Oswaldo Cruz Vol. 111; no. 11; pp. 663 - 669 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Brazil
Instituto Oswaldo Cruz, Ministério da Saúde
01.11.2016
Fundação Oswaldo Cruz (FIOCRUZ) |
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Abstract | Human papillomavirus (HPV) infections are strongly associated with the development of cervical intraepithelial neoplasias and invasive cervical cancer. Polymorphisms in cytokine-encoding genes and behavioural cofactors could play an important role in protecting an individual against viral infections and cancer. Here, we investigated whether IL-6 -174 G>C, IL-8 +396 G>T, and TGF-β1 +869 G>C and +915 G>C polymorphisms were associated with susceptibility to HPV infection in women from north-east (Pernambuco) Brazil. We analysed 108 healthy uninfected women (HC) and 108 HPV-positive women with cervical lesions. Genetic polymorphisms were assessed using Sanger sequencing and polymerase chain reaction-restriction fragment length polymorphism. Comparison of the distribution of the genotypic and allelic frequencies of the IL-18 +396 T>G polymorphism between HPV infected woman an uninfected controls showed that the GG genotype and G allele were both more frequent in the HC group, and were associated with protection from HPV infection (p = 0.0015; OR = 0.29 CI95% = 0.13-0.61; p = 0.0005; OR = 0.45 CI95% 0.29-0.7, respectively). Individuals from the control group could have previously had HPV infection that was spontaneously eliminated; however, it was undetectable at the time of sample collection. Based on our findings, we hypothesize that the IL-8 +396 G>T polymorphism could interfere with susceptibility to HPV infection, by modulating the ability of immune system to fight the virus. |
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AbstractList | Human papillomavirus (HPV) infections are strongly associated with the development of cervical intraepithelial neoplasias and invasive cervical cancer. Polymorphisms in cytokine-encoding genes and behavioural cofactors could play an important role in protecting an individual against viral infections and cancer. Here, we investigated whether IL-6 -174 G>C, IL-8 +396 G>T, and TGF-β1 +869 G>C and +915 G>C polymorphisms were associated with susceptibility to HPV infection in women from north-east (Pernambuco) Brazil. We analysed 108 healthy uninfected women (HC) and 108 HPV-positive women with cervical lesions. Genetic polymorphisms were assessed using Sanger sequencing and polymerase chain reaction-restriction fragment length polymorphism. Comparison of the distribution of the genotypic and allelic frequencies of the IL-18 +396 T>G polymorphism between HPV infected woman an uninfected controls showed that the GG genotype and G allele were both more frequent in the HC group, and were associated with protection from HPV infection (p = 0.0015; OR = 0.29 CI95% = 0.13-0.61; p = 0.0005; OR = 0.45 CI95% 0.29-0.7, respectively). Individuals from the control group could have previously had HPV infection that was spontaneously eliminated; however, it was undetectable at the time of sample collection. Based on our findings, we hypothesize that the IL-8 +396 G>T polymorphism could interfere with susceptibility to HPV infection, by modulating the ability of immune system to fight the virus. Human papillomavirus (HPV) infections are strongly associated with the development of cervical intraepithelial neoplasias and invasive cervical cancer. Polymorphisms in cytokine-encoding genes and behavioural cofactors could play an important role in protecting an individual against viral infections and cancer. Here, we investigated whether IL-6 -174 G>C, IL-8 +396 G>T, and TGF-β1 +869 G>C and +915 G>C polymorphisms were associated with susceptibility to HPV infection in women from north-east (Pernambuco) Brazil. We analysed 108 healthy uninfected women (HC) and 108 HPV-positive women with cervical lesions. Genetic polymorphisms were assessed using Sanger sequencing and polymerase chain reaction-restriction fragment length polymorphism. Comparison of the distribution of the genotypic and allelic frequencies of the IL-18 +396 T>G polymorphism between HPV infected woman an uninfected controls showed that the GG genotype and G allele were both more frequent in the HC group, and were associated with protection from HPV infection (p = 0.0015; OR = 0.29 CI95% = 0.13-0.61; p = 0.0005; OR = 0.45 CI95% 0.29-0.7, respectively). Individuals from the control group could have previously had HPV infection that was spontaneously eliminated; however, it was undetectable at the time of sample collection. Based on our findings, we hypothesize that the IL-8 +396 G>T polymorphism could interfere with susceptibility to HPV infection, by modulating the ability of immune system to fight the virus. Human papillomavirus (HPV) infections are strongly associated with the development of cervical intraepithelial neoplasias and invasive cervical cancer. Polymorphisms in cytokine-encoding genes and behavioural cofactors could play an important role in protecting an individual against viral infections and cancer. Here, we investigated whether IL-6 -174 G>C, IL-8 +396 G>T, and TGF-β1 +869 G>C and +915 G>C polymorphisms were associated with susceptibility to HPV infection in women from north-east (Pernambuco) Brazil. We analysed 108 healthy uninfected women (HC) and 108 HPV-positive women with cervical lesions. Genetic polymorphisms were assessed using Sanger sequencing and polymerase chain reaction-restriction fragment length polymorphism. Comparison of the distribution of the genotypic and allelic frequencies of the IL-18 +396 T>G polymorphism between HPV infected woman an uninfected controls showed that the GG genotype and G allele were both more frequent in the HC group, and were associated with protection from HPV infection (p = 0.0015; OR = 0.29 CI95% = 0.13-0.61; p = 0.0005; OR = 0.45 CI95% 0.29-0.7, respectively). Individuals from the control group could have previously had HPV infection that was spontaneously eliminated; however, it was undetectable at the time of sample collection. Based on our findings, we hypothesize that the IL-8 +396 G>T polymorphism could interfere with susceptibility to HPV infection, by modulating the ability of immune system to fight the virus. |
Author | Macedo, Jamilly Lopes de Moura, Ronald Lima, Júnior, Sérgio Ferreira de Maia, Maria de Mascena Diniz Tavares, Mayara Mansur Fernandes Souza, Paulo Roberto Eleutério de Crovella, Sergio Oliveira, Renata Santos de Heráclio, Sandra de Andrade |
AuthorAffiliation | 6 Universidade Federal de Pernambuco, Departamento de Genética, Recife, PE, Brasil 4 Instituto de Medicina Integral Professor Fernando Figueira, Recife, PE, Brasil 2 Rede Nordeste de Biotecnologia, Recife, PE, Brasil 1 Universidade Federal de Pernambuco, Pós-Graduação em Biologia Aplicada à Saúde, Laboratório de Genoma, Recife, PE, Brasil 3 Universidade Federal Rural de Pernambuco, Recife, PE, Brasil 5 Universidade Federal Rural de Pernambuco,Departamento de Biologia, Recife, PE, Brasil |
AuthorAffiliation_xml | – name: 2 Rede Nordeste de Biotecnologia, Recife, PE, Brasil – name: 5 Universidade Federal Rural de Pernambuco,Departamento de Biologia, Recife, PE, Brasil – name: 3 Universidade Federal Rural de Pernambuco, Recife, PE, Brasil – name: 6 Universidade Federal de Pernambuco, Departamento de Genética, Recife, PE, Brasil – name: 4 Instituto de Medicina Integral Professor Fernando Figueira, Recife, PE, Brasil – name: 1 Universidade Federal de Pernambuco, Pós-Graduação em Biologia Aplicada à Saúde, Laboratório de Genoma, Recife, PE, Brasil – name: Universidade Federal Rural de Pernambuco – name: Universidade Federal de Pernambuco – name: Rede Nordeste de Biotecnologia – name: Instituto de Medicina Integral Professor Fernando Figueira |
Author_xml | – sequence: 1 givenname: Sérgio Ferreira de surname: Lima, Júnior fullname: Lima, Júnior, Sérgio Ferreira de organization: Universidade Federal de Pernambuco, Pós-Graduação em Biologia Aplicada à Saúde, Laboratório de Genoma, Recife, PE, Brasil – sequence: 2 givenname: Mayara Mansur Fernandes surname: Tavares fullname: Tavares, Mayara Mansur Fernandes organization: Universidade Federal de Pernambuco, Pós-Graduação em Biologia Aplicada à Saúde, Laboratório de Genoma, Recife, PE, Brasil – sequence: 3 givenname: Jamilly Lopes de surname: Macedo fullname: Macedo, Jamilly Lopes de organization: Rede Nordeste de Biotecnologia, Recife, PE, Brasil – sequence: 4 givenname: Renata Santos de surname: Oliveira fullname: Oliveira, Renata Santos de organization: Universidade Federal Rural de Pernambuco, Recife, PE, Brasil – sequence: 5 givenname: Sandra de Andrade surname: Heráclio fullname: Heráclio, Sandra de Andrade organization: Instituto de Medicina Integral Professor Fernando Figueira, Recife, PE, Brasil – sequence: 6 givenname: Maria de Mascena Diniz surname: Maia fullname: Maia, Maria de Mascena Diniz organization: Universidade Federal Rural de Pernambuco,Departamento de Biologia, Recife, PE, Brasil – sequence: 7 givenname: Paulo Roberto Eleutério de surname: Souza fullname: Souza, Paulo Roberto Eleutério de organization: Universidade Federal Rural de Pernambuco,Departamento de Biologia, Recife, PE, Brasil – sequence: 8 givenname: Ronald surname: Moura fullname: Moura, Ronald organization: Universidade Federal de Pernambuco, Departamento de Genética, Recife, PE, Brasil – sequence: 9 givenname: Sergio surname: Crovella fullname: Crovella, Sergio organization: Universidade Federal de Pernambuco, Departamento de Genética, Recife, PE, Brasil |
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Cites_doi | 10.1016/j.ejogrb.2011.05.019 10.1128/MMBR.65.1.131-150.2001 10.4238/2015.March.31.18 10.1089/107999001459150 10.1046/j.1365-2370.2002.00347.x 10.1056/NEJMoa021641 10.1073/pnas.91.9.3602 10.1073/pnas.94.7.3052 10.1002/(SICI)1097-0142(19990615)85:12<2526::AID-CNCR6>3.0.CO;2-3 10.2217/fon.12.59 10.3892/ol.2015.3295 10.1172/JCI2629 10.1016/j.clinbiochem.2004.01.014 10.1200/JCO.2005.02.047 10.1158/1055-9965.1547.13.9 10.1016/j.ejogrb.2008.04.007 10.1158/1055-9965.EPI-05-0446 10.1016/j.cyto.2012.04.013 10.1155/2013/146079 10.1016/j.jaci.2010.11.050 10.1016/j.cyto.2010.11.014 10.1215/S1152851704001061 10.1093/oxfordjournals.jncimonographs.a003480 10.1086/321291 10.1038/nrc798 10.2217/pgs.13.238 |
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Keywords | cytokine host genome polymorphisms HPV |
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SubjectTerms | Adolescent Adult Aged Alleles Base Sequence Brazil Cervical Intraepithelial Neoplasia - genetics Cervical Intraepithelial Neoplasia - virology Cross-Sectional Studies cytokine DNA, Viral - analysis Female Gene Frequency Genetic Predisposition to Disease host genome HPV Humans Interleukin-6 - genetics Interleukin-8 - genetics Middle Aged Papillomavirus Infections - genetics Papillomavirus Infections - virology PARASITOLOGY Polymerase Chain Reaction Polymorphism, Single Nucleotide polymorphisms Transforming Growth Factor beta1 - genetics TROPICAL MEDICINE Uterine Cervical Neoplasms - genetics Uterine Cervical Neoplasms - virology Young Adult |
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Title | Influence of IL-6, IL-8, and TGF-β1 gene polymorphisms on the risk of human papillomavirus-infection in women from Pernambuco, Brazil |
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