Are moles determined by genetics?
While the tendency to develop moles appears to be inherited, the specific genetic factors involved are not fully understood.
Overview of Moles
Moles are common overgrowths of skin cells called melanocytes. While they are technically a type of cell overgrowth, they are almost always noncancerous (benign). Moles typically begin to appear in childhood and can change in size, shape, or color throughout a person's life. Factors such as hormonal changes (e.g., during pregnancy or adolescence) and sun exposure can influence their development.
Genetic Factors
Although the exact inheritance pattern is not well understood, the tendency to develop moles appears to run in families. Research has identified several genes involved in the development of benign moles:
- BRAF Gene: This is the most-studied gene related to moles. A variant in BRAF produces an altered protein that causes melanocytes to aggregate into a mole. This protein also triggers the production of a tumor-suppressor protein called p15, which prevents the mole from growing too large.
- Other Genes: Variations in genes such as FGFR3, PIK3CA, and HRAS are also associated with benign moles.
Moles and Cancer Risk
In rare cases, the interaction between genetic variants and environmental factors can lead to malignancy:
- Malignant Transformation: If a BRAF gene variant is combined with the loss (deletion) of the CDKN2A gene, the body may fail to produce p15, potentially allowing mole cells to grow uncontrollably.
- Sun Exposure: Ultraviolet radiation can damage existing moles. Individuals with fair skin, a family history of melanoma, or a high number of moles are at an increased risk.
- Atypical Moles: Large, irregularly shaped moles known as dysplastic nevi are linked to heredity and can increase a person's risk of developing melanoma.
Because melanoma can develop in areas not exposed to the sun, researchers continue to study susceptibility genes to better understand the relationship between moles and skin cancer.