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Assessment of TP53 Polymorphisms and MDM2 SNP309 in Premenopausal Breast Cancer Risk.
Samuel, Nardin; Id Said, Badr; Guha, Tanya; Novokmet, Ana; Li, Weili; Silwal-Pandit, Laxmi; Børrsen-Dale, Anne-Lise; Langerød, Anita; Hudson, Thomas J; Malkin, David.
Afiliação
  • Samuel N; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
  • Id Said B; Department of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Guha T; Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
  • Novokmet A; Department of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Li W; Department of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Silwal-Pandit L; Department of Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Børrsen-Dale AL; The Centre for Applied Genomics, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Langerød A; Department of Genetics, Institute for Cancer Research, The K.G. Jebsen Center for Breast Cancer Research, Institute for Clinical Medicine, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
  • Hudson TJ; Department of Genetics, Institute for Cancer Research, The K.G. Jebsen Center for Breast Cancer Research, Institute for Clinical Medicine, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
  • Malkin D; Department of Genetics, Institute for Cancer Research, The K.G. Jebsen Center for Breast Cancer Research, Institute for Clinical Medicine, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Hum Mutat ; 38(3): 265-268, 2017 03.
Article em En | MEDLINE | ID: mdl-27957778
ABSTRACT
Germline polymorphic variants in cancer predisposition genes such as TP53 have been shown to impact the risk of premenopausal cancer. Accordingly, the aim of this study was to assess the spectrum of polymorphisms in TP53 and its negative regulatory gene, MDM2 (SNP309T>G) in patients with premenopausal breast cancer. Our findings in a cohort of 40 female patients demonstrate no significant correlation between the studied polymorphisms and risk of premenopausal breast cancer. Although one polymorphism is found in high frequency in this cohort (rs1800372A>G, 9.0%), it was not associated with the risk of developing cancer before the age of 35 years in an extended cohort of 1,420 breast cancer cases. Functional studies of the rs1800372A>G polymorphic allele reveal that it does not affect p53 transactivation function. Further study of variants or mutations in other cancer susceptibility genes is warranted to refine our understanding of the germline contribution to premenopausal breast cancer susceptibility.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proteína Supressora de Tumor p53 / Pré-Menopausa / Polimorfismo de Nucleotídeo Único / Proteínas Proto-Oncogênicas c-mdm2 Tipo de estudo: Etiology_studies Limite: Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proteína Supressora de Tumor p53 / Pré-Menopausa / Polimorfismo de Nucleotídeo Único / Proteínas Proto-Oncogênicas c-mdm2 Tipo de estudo: Etiology_studies Limite: Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article