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The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium.
Ugai, Tomotaka; Milne, Roger L; Ito, Hidemi; Aronson, Kristan J; Bolla, Manjeet K; Chan, Tsun; Chan, Ching W; Choi, Ji-Yeob; Conroy, Don M; Dennis, Joe; Dunning, Alison M; Easton, Douglas F; Gaborieau, Valerie; Gonzalez-Neira, Anna; Hartman, Mikael; Healey, Catherine S; Iwasaki, Motoki; John, Esther M; Kang, Daehee; Kim, Sung-Won; Kwong, Ava; Lophatananon, Artitaya; Michailidou, Kyriaki; Taib, Nur Aishah Mohd; Muir, Kenneth; Park, Sue K; Pharoah, Paul D P; Sangrajrang, Suleeporn; Shen, Chen-Yang; Shu, Xiao-Ou; Spinelli, John J; Teo, Soo H; Tessier, Daniel C; Tseng, Chiu-Chen; Tsugane, Shoichiro; Vincent, Daniel; Wang, Qin; Wu, Anna H; Wu, Pei-Ei; Zheng, Wei; Matsuo, Keitaro.
Afiliação
  • Ugai T; Division of Cancer Epidemiology and Prevention, Department of Preventive Medicine, Aichi Cancer Center Research Institute, Nagoya, Japan.
  • Milne RL; Cancer Epidemiology & Intelligence Division, Melbourne, VIC, Australia.
  • Ito H; Centre for Epidemiology and Biostatistics, School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia.
  • Aronson KJ; Division of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center Research Institute, Nagoya, Japan.
  • Bolla MK; Department of Epidemiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Chan T; Department of Public Health Sciences, Queen's Cancer Institute, Queen's University, Kingston, Ontario, Canada.
  • Chan CW; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Choi JY; Hong Kong Hereditary Breast Cancer Family Registry, Happy Valley, Hong Kong.
  • Conroy DM; Department of Pathology, Hong Kong Sanatorium and Hospital, Happy Valley, Hong Kong.
  • Dennis J; Department of Surgery, National University Health System, Singapore.
  • Dunning AM; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
  • Easton DF; Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Gaborieau V; Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Gonzalez-Neira A; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Hartman M; Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Healey CS; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Iwasaki M; Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK.
  • John EM; Genetic Epidemiology Group, International Agency for Research on Cancer, Lyon, France.
  • Kang D; Human Cancer Genetics Program, Spanish National Cancer Research Centre, Madrid, Spain.
  • Kim SW; Department of Surgery, National University Health System, Singapore.
  • Kwong A; Saw Swee Hock School of Public Health, National University of Singapore, Singapore.
  • Lophatananon A; Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Michailidou K; Epidemiology and Prevention Group, Center for Public Health Sciences, National Cancer Center, Tokyo, Japan.
  • Taib NAM; Department of Medicine and Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California, USA.
  • Muir K; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
  • Park SK; Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Pharoah PDP; Department of Preventive Medicine, Seoul National University College of Medicine, Seoul National University, Seoul, Korea.
  • Sangrajrang S; Department of Surgery, Daerim Saint Mary's Hospital, Seoul, Korea.
  • Shen CY; Hong Kong Hereditary Breast Cancer Family Registry, Happy Valley, Hong Kong.
  • Shu XO; Department of Surgery, Queen Mary Hospital, The University of Hong Kong, Happy Valley, Hong Kong.
  • Spinelli JJ; Department of Surgery, Hong Kong Sanatorium and Hospital, Happy Valley, Hong Kong.
  • Teo SH; Division of Health Sciences, Warwick Medical School, Warwick University, Coventry, UK.
  • Tessier DC; Division of Population Sciences, Warwick Medical School, Warwick University, Coventry, UK.
  • Tseng CC; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Tsugane S; Department of Electron Microscopy/Molecular Pathology, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
  • Vincent D; Breast Cancer Research Unit, University Malaya Cancer Research Institute, University Malaya Medical Centre, Kuala Lumpur, Malaysia.
  • Wang Q; Division of Health Sciences, Warwick Medical School, Warwick University, Coventry, UK.
  • Wu AH; Division of Population Sciences, Warwick Medical School, Warwick University, Coventry, UK.
  • Wu PE; Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Korea.
  • Zheng W; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
  • Matsuo K; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Mol Genet Genomic Med ; 7(6): e707, 2019 06.
Article em En | MEDLINE | ID: mdl-31066241
ABSTRACT

BACKGROUND:

Epidemiological studies consistently indicate that alcohol consumption is an independent risk factor for female breast cancer (BC). Although the aldehyde dehydrogenase 2 (ALDH2) polymorphism (rs671 Glu>Lys) has a strong effect on acetaldehyde metabolism, the association of rs671 with BC risk and its interaction with alcohol intake have not been fully elucidated. We conducted a pooled analysis of 14 case-control studies, with individual data on Asian ancestry women participating in the Breast Cancer Association Consortium.

METHODS:

We included 12,595 invasive BC cases and 12,884 controls for the analysis of rs671 and BC risk, and 2,849 invasive BC cases and 3,680 controls for the analysis of the gene-environment interaction between rs671 and alcohol intake for BC risk. The pooled odds ratios (OR) with 95% confidence intervals (CI) associated with rs671 and its interaction with alcohol intake for BC risk were estimated using logistic regression models.

RESULTS:

The Lys/Lys genotype of rs671 was associated with increased BC risk (OR = 1.16, 95% CI 1.03-1.30, p = 0.014). According to tumor characteristics, the Lys/Lys genotype was associated with estrogen receptor (ER)-positive BC (OR = 1.19, 95% CI 1.05-1.36, p = 0.008), progesterone receptor (PR)-positive BC (OR = 1.19, 95% CI 1.03-1.36, p = 0.015), and human epidermal growth factor receptor 2 (HER2)-negative BC (OR = 1.25, 95% CI 1.05-1.48, p = 0.012). No evidence of a gene-environment interaction was observed between rs671 and alcohol intake (p = 0.537).

CONCLUSION:

This study suggests that the Lys/Lys genotype confers susceptibility to BC risk among women of Asian ancestry, particularly for ER-positive, PR-positive, and HER2-negative tumor types.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Polimorfismo de Nucleotídeo Único / Aldeído-Desidrogenase Mitocondrial Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Polimorfismo de Nucleotídeo Único / Aldeído-Desidrogenase Mitocondrial Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Japão