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Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study.
Leo, Paul J; Madeleine, Margaret M; Wang, Sophia; Schwartz, Stephen M; Newell, Felicity; Pettersson-Kymmer, Ulrika; Hemminki, Kari; Hallmans, Goran; Tiews, Sven; Steinberg, Winfried; Rader, Janet S; Castro, Felipe; Safaeian, Mahboobeh; Franco, Eduardo L; Coutlée, François; Ohlsson, Claes; Cortes, Adrian; Marshall, Mhairi; Mukhopadhyay, Pamela; Cremin, Katie; Johnson, Lisa G; Trimble, Cornelia L; Garland, Suzanne; Tabrizi, Sepehr N; Wentzensen, Nicolas; Sitas, Freddy; Little, Julian; Cruickshank, Maggie; Frazer, Ian H; Hildesheim, Allan; Brown, Matthew A.
Afiliação
  • Leo PJ; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.
  • Madeleine MM; Program in Epidemiology, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
  • Wang S; Department of Population Sciences, Beckman Research Institute, City of Hope, Duarte, CA, United States of America.
  • Schwartz SM; Program in Epidemiology, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
  • Newell F; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.
  • Pettersson-Kymmer U; Department of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden.
  • Hemminki K; Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
  • Hallmans G; Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Tiews S; Center for Primary Health Care Research, Lund University, Lund, Sweden.
  • Steinberg W; Nutritional Research, Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
  • Rader JS; MHC Laboratory for Cytopathology, Dr.Steinberg GmbH, Soest, Germany.
  • Castro F; MHC Laboratory for Cytopathology, Dr.Steinberg GmbH, Soest, Germany.
  • Safaeian M; Department of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America.
  • Franco EL; Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Coutlée F; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, United States of America.
  • Ohlsson C; Division of Cancer Epidemiology, McGill University, Montreal, QC, Canada.
  • Cortes A; Département de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, QC, Canada.
  • Marshall M; Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy University of Gothenburg, Gothenburg, Sweden.
  • Mukhopadhyay P; Centre for Bone and Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Cremin K; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.
  • Johnson LG; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.
  • Trimble CL; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.
  • Garland S; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.
  • Tabrizi SN; Program in Epidemiology, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.
  • Wentzensen N; Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
  • Sitas F; Regional World Health Organisation Human Papillomavirus Laboratory Network, Department of Microbiology and Infectious Diseases, The Royal Women's Hospital, Parkville, Victoria, 3052, Australia.
  • Little J; Department of Obstetrics and Gynaecology, University of Melbourne, Murdoch Childrens Research Institute, The Royal Children's Hospital, Parkville, Victoria, 3052, Australia.
  • Cruickshank M; Department of Obstetrics and Gynaecology, University of Melbourne, Murdoch Childrens Research Institute, The Royal Children's Hospital, Parkville, Victoria, 3052, Australia.
  • Frazer IH; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, United States of America.
  • Hildesheim A; Cancer Council NSW, Sydney, NSW, Australia.
  • Brown MA; Sydney School of Public Health, University of Sydney, Camperdown, NSW, Australia.
PLoS Genet ; 13(8): e1006866, 2017 08.
Article em En | MEDLINE | ID: mdl-28806749
A small percentage of women with cervical HPV infection progress to cervical neoplasia, and the risk factors determining progression are incompletely understood. We sought to define the genetic loci involved in cervical neoplasia and to assess its heritability using unbiased unrelated case/control statistical approaches. We demonstrated strong association of cervical neoplasia with risk and protective HLA haplotypes that are determined by the amino-acids carried at positions 13 and 71 in pocket 4 of HLA-DRB1 and position 156 in HLA-B. Furthermore, 36% (standard error 2.4%) of liability of HPV-associated cervical pre-cancer and cancer is determined by common genetic variants. Women in the highest 10% of genetic risk scores have approximately >7.1% risk, and those in the highest 5% have approximately >21.6% risk, of developing cervical neoplasia. Future studies should examine genetic risk prediction in assessing the risk of cervical neoplasia further, in combination with other screening methods.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos HLA-B / Neoplasias do Colo do Útero / Predisposição Genética para Doença / Estudo de Associação Genômica Ampla / Cadeias HLA-DRB1 Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos HLA-B / Neoplasias do Colo do Útero / Predisposição Genética para Doença / Estudo de Associação Genômica Ampla / Cadeias HLA-DRB1 Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article