Skin cancer risk in hereditary mixed cancer syndromes
Veera Nikkola, Anna Alakoski, Jukka-Pekka Mecklin, Toni T. Seppälä, Jussi Nikkola, Kashmintan Schrader

TL;DR
This paper reviews how certain inherited genetic conditions increase the risk of skin cancers and suggests tailored screening and prevention strategies.
Contribution
The paper highlights underrecognized skin cancer risks in hereditary cancer syndromes and recommends dermatologic evaluations for affected individuals.
Findings
Li-Fraumeni, Lynch, and HBOC syndromes are linked to increased skin cancer risks.
Pathogenic ATM and CHEK2 variants may predispose individuals to skin cancers.
Dermatologic evaluation and UV protection strategies are recommended for early detection.
Abstract
Hereditary cancer syndromes are genetic conditions that increase an individual’s risk for multiple cancer types, often due to mutations that affect critical cellular processes such as DNA repair and cell cycle regulation. Skin cancers, including malignant melanoma (MM), basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and related precancerous lesions may be underrecognized in some hereditary cancer syndromes, as suggested by underlying biological mechanisms and their underreporting in studies. In this narrative review, we examine the skin cancer risks associated with the most prevalent hereditary cancer syndromes, including Li-Fraumeni syndrome (LFS), Lynch syndrome (LS), hereditary breast and ovarian cancer syndrome (HBOC), ATM-associated hereditary cancer syndrome, CHEK2-associated hereditary cancer syndrome, BRIP1-associated cancer predisposition, and hereditary…
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Taxonomy
TopicsDNA Repair Mechanisms · Genetic factors in colorectal cancer · BRCA gene mutations in cancer
