Professor Gareth Evans of the University of Manchester, the
lead author of the study, said it was 'likely that these women inherit genetic
factors other than BRCA-related genes that increase their breast cancer risk'.
The researchers analysed data from 807 families with a
history of carrying either the BRCA1 or BRCA2 gene mutation. Forty-nine women from
these families tested negative for their family-specific mutation but went on
to develop breast cancer.
The researchers noted four and a half times the number of breast cancers
in non-carrier women from BRCA2 families than would be expected in women of
the same age in the general population. However, the incidence of breast cancer in test-negative
women from BRCA1 families was not significantly increased.
Professor Evans suggests that families who carry BRCA2 may
be more likely to carry other cancer risk mutations.
'Around 77 single nucleotide polymorphisms (SNPs) are linked to breast cancer risk', he said. 'Identification
of additional SNPs is necessary to understand why some of the BRCA-negative
women from BRCA families are at higher risk'.
BRCA genes are 'tumour suppressor genes', encoding proteins that help the body repair damaged DNA. Inheriting faulty copies of these genes
allows genetic damage to accumulate in cells, which might potentially lead to
breast or ovarian cancer.
This new research may have implications for genetic counselling of women who test negative for BRCA2 mutations.
'Providing patients with
accurate information on their risk of developing breast cancer in the future is
critical for decision-making regarding different options and interventions', confirmed Dr Elisa Port, from the Dubin Breast
Center in New York, USA, speaking to HealthDay News.