Breast and ovarian cancer | Go Back |
It is not intended to give a comprehensive overview of breast and ovarian cancer genetics on these pages; instead links are provided to relevant websites for further information.
Breast cancer is a common disease and it is likely that at least 1 in 9 women in the UK will develop it during their lifetime, so it is not unusual for a patient to have one or two relatives who have developed breast cancer by chance. Ovarian cancer is less common, with 1 in 48 women developing ovarian cancer during their lifetime.
The development and progression of both breast and ovarian cancers can involve several factors, such as environmental, lifestyle, reproductive, and genetic factors.
A significant family history
- Breast and ovarian cancers that have occurred in a family are more likely to be significant if:
- There is more than one case of breast cancer on the same side of the family
- The cancers were diagnosed at a young age (e.g. before the menopause)
- The people who have had breast cancer are closely related (first and second-degree) blood relatives of the patient - such as mother, aunt, grandmother, sisters.
- A close relative of the patient has had bilateral breast cancer.
- The patient is of Eastern European and/or Jewish descent.
Cancer susceptibility genes:
Two dominant breast cancer susceptibility genes have been identified to date: BRCA1 and BRCA2. The identification of other cancer susceptibility genes is the subject of ongoing research. Mutations in BRCA1 and BRCA2 only account for less than 2% of all breast cancers. Although the absolute numbers are small, it is important to identify susceptible individuals because of the high risk of developing tumours. |
| Tumour associationsBRCA1
BRCA2
Lower risk: Hodgkin's lymphoma, gallbladder (influenced by mutation) |
This page was last modified on Thu Oct 01 2009



