Breast Cancer

In-Depth Analysis

Risk Factors

Genetic Mutations and Family History

Genomic variables account for a portion of the major “Breast cancer” risk factors. Elevated risk of breast and ovarian cancer is associated with mutations in certain genes, such as BRCA1 and BRCA2 (Pourmasoumi, Moradi & Bayat, 2024). These genes are supposed to work to repair DNA damage and suppress the growth of tumours, but inherited mutations disable them, allowing cancer cells to grow undisturbed. A woman's lifetime risk of getting breast cancer may reach 70% if she had mutations in either BRCA1 or BRCA2. The increased risk of developing “Breast cancer” can also be seen in individuals who have genetic mutations other than BRCA, for example, “TP53, CHEK2, and PALB2” (Graffeo et al., 2022). Through genetic testing, individuals at risk can be identified early and offered preventive measures in the form of enhanced screening or prophylactic surgery.

Lifestyle and Environmental Influences

The very environment one lives in, as well as lifestyle scenarios and choices, contribute immensely to the risk factors for “Breast cancer”, which is another important area needing focus apart from genetics and hormones. Many of these will lend themselves to modification, and hence, lifestyle changes constitute a fundamental aspect of “Breast cancer” prevention.

Obesity, Physical Inactivity, and Diet

A well-established risk factor for the development of “Breast cancer” is excess body weight, especially after menopause. Fat cells create estragon, and more fat creates more estragon, which can stimulate hormone-sensitive “Breast cancers' growth. A Body Mass Index above 30 significantly increases the risk compared with a healthy BMI (Mohanty & Mohanty, 2021).