AI Article Synopsis

  • About 5%-10% of breast cancers are linked to genetic factors, particularly due to mutations in BRCA1 and BRCA2 genes.
  • The study reviews data from 11 Asian countries and ethnic Asian populations in North America to analyze the variations and commonality of these mutations.
  • Knowledge of BRCA1/BRCA2 mutation patterns in Asian populations can improve breast cancer risk assessment and treatment strategies.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681590PMC
http://dx.doi.org/10.1136/jmedgenet-2015-103132DOI Listing

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