The exact causes of breast cancer are largely unknown, but both environmental and genetic factors are involved. Specific mutations in genes called HER2, BRCA1, BRCA2, CHEK2, and p53 have been linked to breast cancer; these mutations may be inherited or acquired. Mutations that are inherited often substantially increase a person’s risk for developing breast cancer. For example, whereas some 12 percent of women in the general population develop breast cancer, roughly 60 percent of women who inherit mutations in BRCA1 or BRCA2 eventually develop the disease. Women who carry these mutations also have an increased risk of ovarian cancer. About 5 to 10 percent of men carrying BRCA2 mutations will develop breast cancer in their lifetimes; the risk is lower, about 1 to 2 percent, for men carrying BRCA1 mutations.
In addition to genetic mutations, other factors, including prolonged exposure to the hormone estrogen, as when menstruation starts before age 12 and continues beyond age 50, favour the development of cancer. In postmenopausal women, breast cancer risk is increased markedly by elevated circulating concentrations of sex hormones (estrogens and androgens). Concentrations of these hormones have been found to be abnormally high in postmenopausal women who are obese, who drink alcohol, or who smoke. In addition, for all women, lack of exercise, obesity, use of oral contraceptives, alcohol consumption, smoking, and previous medical treatments involving chest irradiation are considered risk factors for breast cancer. Women who have had certain kinds of benign tumours are also more prone to developing breast cancer.
The most common symptom of breast cancer is an abnormal lump or swelling in the breast, but lumps may also appear beside the breast or under the arm. Other symptoms may include unexplained breast pain, abnormal nipple discharge, changes in breast texture, or changes in the skin on or around the breast.

Diagnosis

Early diagnosis greatly improves the odds of survival. When detected early, breast cancer has a very high five-year survival rate, and patients who reach this stage often go on to live long, healthy lives. Survival rates are lower for cancers that have spread locally, and they are very low for cancers that have metastasized, or spread, to distant parts of the body.
Breast cancer may be discovered by the patient during a regular breast self-examination. When a self-exam is performed on a monthly basis, a woman becomes familiar with her breasts and can readily detect an abnormal change, such as a lump, a swelling, dimpling, or a change in contour, warranting immediate clinical examination. However, a change that is noticed through self-examination may not always be indicative of cancer. Alternatively, if the change found is cancer, the growth may already be fairly advanced.
Before they are palpable, growths in the breast may be detected through a procedure known as mammography, which entails the use of X-rays to detect lesions in breast tissue. Mammography is often used for initial diagnosis, but, in order to confirm the presence of cancer, a tissue sample (biopsy) usually must be taken. If cancer is suspected to have spread (metastasized) to nearby lymph nodes, they must also be sampled. Metastasis generally begins in a so-called sentinel lymph node (the first lymph node invaded by cancer cells) and, in the case of breast cancer, spreads to axillary lymph nodes, which are located in and around the armpits.
Once cancer has been diagnosed, the tumour’s type and degree of invasiveness is assessed. Several imaging methods may be used to determine the degree of metastasis, including X-rays, computerized axial tomography (CAT) scans, or magnetic resonance imaging (MRI). The presence of receptors for the hormones estrogen and progesterone is also determined because these receptors play an important role in the cancer’s development and in decisions regarding the appropriate treatment.