Patients with germline mutations in BRCA1 or BRCA2 genes are predisposed to breast cancer. The BRCA1-associated breast cancers have distinct morphology, being more often medullary-like, triple negative and showing a 'basal' phenotype. On the other hand, BRCA2 and BRCAX cancers are a heterogeneous group without a specific phenotype. When incorporated into risk assessment models, pathology data improves prediction of carrier status. The role of BRCA1 and BRCA2 in DNA repair is being exploited to develop novel therapies, for example, using the poly-ADP-ribose polymerase inhibitors. A number of low-to-moderatepenetrant genes/loci have also been identified, but their role and contribution in breast cancer development is still under investigation. Modern Pathology (2010) 23, S46-S51; doi:10.1038/modpathol.2010.37Keywords: BRCA1; BRCA2; BRCAX; breast; hereditary cancer Breast cancer is the commonest malignancy in women and it is estimated that a million women worldwide will develop breast cancer each year. A number of risk factors have been identified including early menarche, late menopause, nulliparity and a positive family history.1 First-degree relatives have an approximately twofold increase in risk of developing the disease. A number of highly penetrant breast cancer susceptibility genes have been identified and include BRCA1 and BRCA2.2,3 These genes confer a high risk of breast and ovarian carcinoma. Two genes associated with rare cancer syndromes, P53 (Li-Fraumeni syndrome) 4 and PTEN (Cowden syndrome) 5 also confer a very high risk of breast cancer. Although all these genes confer a very high risk, they account for a relatively small proportion of inherited breast cancers. It has become increasingly clear that overall susceptibility to breast cancer is likely to be mediated through variants in many genes, each conferring a small-to-moderate risk of the disease. A number of such genes have been reported in the literature and include CHEK2, ATM, NBS1, RAD51, BRIP1 and PALB2.6-10 It is not known how many more genes that confer a small risk are yet to be identified or how these genes come together or interact with each other or with environmental factors to increase the breast cancer risk.
BRCA1, BRCA2 and BRCAXThe first high-penetrance gene, BRCA1, was isolated in the year 1994 2,11 and a year later, BRCA2 was localised and cloned. 3,12 Over the last decade, it has been shown that breast cancer arising in patients harbouring a germline mutation in BRCA1 and BRCA2 genes differs from age-matched sporadic breast cancer cases and from familial breast cancers arising in non-BRCA1/2 patients. These differences are in morphology, immunophenotype and molecular characteristics.3,12-29 These differences tell us something about the biology of familial breast cancer, but could also potentially be used in cancer clinics to predict which patients may harbour BRCA1 germline mutation.
Cellular Functions of BRCA1 and BRCA2BRCA1 has several cellular roles. It has been implicated in DNA repair, cell-cycle regulation, transcription...