Impact of functional germline variants and a deletion polymorphism in APOBEC3A and APOBEC3B on breast cancer risk and survival in ... View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2015-08-31

AUTHORS

Stella Göhler, Miguel Inacio Da Silva Filho, Robert Johansson, Kerstin Enquist-Olsson, Roger Henriksson, Kari Hemminki, Per Lenner, Asta Försti

ABSTRACT

PurposeThe C → T mutation signature caused by APOBEC family members contributes to the development of breast cancer (BC). Also overexpression of APOBEC3B and a ~29.5-kb deletion polymorphism between APOBEC3A and APOBEC3B have been associated with increased BC risk.MethodsWe investigated in a population-based study, with 782 Swedish BC cases and 1559 controls, associations between potentially functional germline variants in APOBEC3A or APOBEC3B gene and BC risk and survival. Additionally, we identified deletion polymorphism carriers and explored possible associations with BC.ResultsNo evidence of association between any germline variant, including the deletion polymorphism, and BC risk or survival was observed. Only APOBEC3A promoter polymorphism rs5757402 was associated with low stage (OR = 0.69, 95 % CI 0.50–0.96, dominant model).ConclusionThe reported association between the deletion polymorphism and BC risk was not confirmed in the Swedish population, nor did any genotyped germline variant show any association with BC risk or survival. More... »

PAGES

273-276

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00432-015-2038-7

DOI

http://dx.doi.org/10.1007/s00432-015-2038-7

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1000333297

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/26320772


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