Influence of germline genetic variants on dermoscopic features of melanoma. (31st January 2021)

• Record Type: Journal Article
• Authors: Pozzobon, Flavia Carolina; Tell‐Marti, Gemma; Calbet‐Llopart, Neus; Barreiro, Alicia; Espinosa, Natalia; Potrony, Míriam; Alejo, Beatriz; Podlipnik, Sebastian; Combalia, Marc; Puig‐Butillé, Joan Anton; Carrera, Cristina; Malvehy, Josep; Puig, Susana
• Is Part Of: Pigment cell & melanoma research. Volume 34:Number 3(2021)
• Page Start: 618
• Page End: 628
• Publication Date: 2021-01-31
• Subjects: dermatoscopy -- dermoscopy -- gene -- germline variants -- MC1R -- melanoma -- nevus; Melanoma -- Periodicals; Chromatophores -- Periodicals; Animal pigments -- Periodicals; 616.99477
• DOI: 10.1111/pcmr.12954
• Languages: English
• ISSNs: 1755-1471

Abstract

Abstract: Nevus count is highly determined by inherited variants and has been associated with the origin of melanoma. D e novo melanomas (DNMMs) are more prevalent in patients with a low nevus count and have distinctive dermoscopic features than nevus‐associated melanomas. We evaluated the impact of nine single nucleotide polymorphisms (SNPs) of MTAP (rs10811629, rs2218220, rs7023329 and rs751173), PLA2G6 (rs132985 and rs2284063), IRF4 (rs12203592), and PAX3 (rs10180903 and rs7600206) genes associated with nevus count and melanoma susceptibility, and the MC1R variants on dermoscopic features of 371 melanomas from 310 patients. All MTAP variants associated with a low nevus count were associated with regression structures (peppering and mixed regression), blue‐whitish veil, shiny white structures, and pigment network. SNPs of PLA2G6 (rs132985), PAX3 (rs7600206), and IRF4 (rs12203592) genes were also associated with either shiny white structures or mixed regression (all corrected p ‐values ≤ .06). Melanomas from red hair color MC1R variants carriers showed lower total dermoscopy score ( p ‐value = .015) and less blotches than melanomas from non‐carriers ( p ‐value = .048). Our results provide evidence that germline variants protective for melanoma risk and/or associated with a low nevus count are associated with certain dermoscopic features, more characteristic of de novo and worse prognosis melanomas.