Genotype-phenotype correlations in patients with breast cancer and BRCA1 mutations (4153delA, 185delAG, 5382insC)

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Abstract

Hereditary breast cancer (BC) associated with BRCA1 mutations is characterized by a number of features as compared to sporadic and BRCA2- associated BC. Structural and functional changes in mutant proteins in accordance with the type and locus of BRCA1 mutations determine different variants of a BC phenotype. Identification of genotype-phenotype correlations in patients with hereditary BC makes it possible to single out its basic characteristics, to personalize its diagnosis and treatment, to estimate the prognosis and risk of multiple primary tumors in accordance with BRCA1 mutations (4153delA, 185delAG, 5382insC).

About the authors

Ye. M. Bit-Sava

Saint Petersburg State Pediatric Medical University, Ministry of Health of Russia
Acad. I.P. Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia

Author for correspondence.
Email: bit-sava@mail.ru
Russian Federation

V. F. Semiglazov

N.N. Petrov Oncology Research Institute, Ministry of Health of Russia, Saint Petersburg

Russian Federation

Ye. N. Imyanitov

Saint Petersburg State Pediatric Medical University, Ministry of Health of Russia
N.N. Petrov Oncology Research Institute, Ministry of Health of Russia, Saint Petersburg

Russian Federation

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