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Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.
Kwong, Ava; Shin, Vivian Y; Ho, John C W; Kang, Eunyoung; Nakamura, Seigo; Teo, Soo-Hwang; Lee, Ann S G; Sng, Jen-Hwei; Ginsburg, Ophira M; Kurian, Allison W; Weitzel, Jeffrey N; Siu, Man-Ting; Law, Fian B F; Chan, Tsun-Leung; Narod, Steven A; Ford, James M; Ma, Edmond S K; Kim, Sung-Won.
Afiliação
  • Kwong A; Department of Surgery, The University of Hong Kong, Hong Kong, Hong Kong Hong Kong Hereditary Breast Cancer Family Registry, Hong Kong, Hong Kong Departments of Medicine (Oncology) and Genetics, Stanford University School of Medicine, Stanford, California, USA Department of Surgery, Hong Kong Sanato
  • Shin VY; Department of Surgery, The University of Hong Kong, Hong Kong, Hong Kong.
  • Ho JC; Department of Surgery, The University of Hong Kong, Hong Kong, Hong Kong Department of Molecular Pathology, Hong Kong Sanatorium & Hospital, Hong Kong, Hong Kong.
  • Kang E; Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
  • Nakamura S; Department of Surgery, Division of Breast Surgical Oncology, Showa University School of Medicine, Tokyo, Japan.
  • Teo SH; Cancer Research Initiatives Foundation, Sime Darby Medical Centre, Subang Jaya, Selangor, Malaysia Faculty of Medicine, University Malaya Cancer Research Institute, University Malaya, Subang Jaya, Malaysia.
  • Lee AS; Division of Medical Sciences, National Cancer Centre, Singapore, Singapore Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore Office of Clinical & Academic Faculty Affairs, Duke-NUS Graduate Medical School, Singapore, Singapore.
  • Sng JH; Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Ginsburg OM; Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada.
  • Kurian AW; Departments of Medicine (Oncology) and Genetics, Stanford University School of Medicine, Stanford, California, USA.
  • Weitzel JN; Division of Clinical Cancer Genetics, City of Hope National Medical Center, Duarte, California, USA.
  • Siu MT; Department of Surgery, The University of Hong Kong, Hong Kong, Hong Kong.
  • Law FB; Hong Kong Hereditary Breast Cancer Family Registry, Hong Kong, Hong Kong Department of Molecular Pathology, Hong Kong Sanatorium & Hospital, Hong Kong, Hong Kong.
  • Chan TL; Hong Kong Hereditary Breast Cancer Family Registry, Hong Kong, Hong Kong Department of Molecular Pathology, Hong Kong Sanatorium & Hospital, Hong Kong, Hong Kong.
  • Narod SA; Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada.
  • Ford JM; Departments of Medicine (Oncology) and Genetics, Stanford University School of Medicine, Stanford, California, USA.
  • Ma ES; Hong Kong Hereditary Breast Cancer Family Registry, Hong Kong, Hong Kong Department of Molecular Pathology, Hong Kong Sanatorium & Hospital, Hong Kong, Hong Kong.
  • Kim SW; Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
J Med Genet ; 53(1): 15-23, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26187060
Approximately 5%-10% of breast cancers are due to genetic predisposition caused by germline mutations; the most commonly tested genes are BRCA1 and BRCA2 mutations. Some mutations are unique to one family and others are recurrent; the spectrum of BRCA1/BRCA2 mutations varies depending on the geographical origins, populations or ethnic groups. In this review, we compiled data from 11 participating Asian countries (Bangladesh, Mainland China, Hong Kong SAR, Indonesia, Japan, Korea, Malaysia, Philippines, Singapore, Thailand and Vietnam), and from ethnic Asians residing in Canada and the USA. We have additionally conducted a literature review to include other Asian countries mainly in Central and Western Asia. We present the current pathogenic mutation spectrum of BRCA1/BRCA2 genes in patients with breast cancer in various Asian populations. Understanding BRCA1/BRCA2 mutations in Asians will help provide better risk assessment and clinical management of breast cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Mutação em Linhagem Germinativa / Genes BRCA1 / Predisposição Genética para Doença / Genes BRCA2 / Mutação Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: J Med Genet Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Mutação em Linhagem Germinativa / Genes BRCA1 / Predisposição Genética para Doença / Genes BRCA2 / Mutação Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: J Med Genet Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido