Genome-wide analysis of constitutional DNA methylation in familial melanoma

Salgado, C.; Gruis, N.; Heijmans, B.T.; Oosting, J.; Doorn, R. van; BIOS Consortium (2020)

Article / Letter to editor

Background Heritable epigenetic alterations have been proposed as an explanation for familial clustering of melanoma. Here we performed genome-wide DNA methylation analysis on affected family members not carrying pathogenic variants in established melanoma susceptibility genes, compared with healthy volunteers. Results All melanoma susceptibility genes showed the absence of epimutations in familial melanoma patients, and no loss of imprinting was detected. Unbiased genome-wide DNA methylation analysis revealed significantly different levels of methylation in single CpG sites. The methylation level differences were small and did not affect reported tumour predisposition genes. Conclusion Our results provide no support for heritable epimutations as a cause of familial melanoma.

• Epimutation
• Loss of imprinting
• DNA methylation
• Familial melanoma

• All authors: Salgado, C.; Gruis, N.; Heijmans, B.T.; Oosting, J.; Doorn, R. van; BIOS Consortium
• Date: 2020-03-06
• Journal: Clinical Epigenetics
• Volume: 12
• Issue: 1
• DOI: doi:10.1186/s13148-020-00831-7
• Link: https://clinicalepigeneticsjournal.biomedcentral.com/articles/10.1186/s1...