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A Mutational Survey of Acral Nevi.
Smalley, Keiran S M; Teer, Jamie K; Chen, Y Ann; Wu, Jheng-Yu; Yao, Jiqiang; Koomen, John M; Chen, Wei-Shen; Rodriguez-Waitkus, Paul; Karreth, Florian A; Messina, Jane L.
Afiliação
  • Smalley KSM; Department of Tumor Biology, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Teer JK; Department of Cutaneous Oncology, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Chen YA; Department of Biostatistics and Bioinformatics, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Wu JY; Department of Biostatistics and Bioinformatics, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Yao J; Department of Tumor Biology, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Koomen JM; Biostatistics and Bioinformatics Shared Resource, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Chen WS; Department of Molecular Oncology, Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Rodriguez-Waitkus P; Department of Dermatology and Cutaneous Surgery, University of South Florida Morsani College of Medicine, Tampa, Florida.
  • Karreth FA; Department of Dermatology and Cutaneous Surgery, University of South Florida Morsani College of Medicine, Tampa, Florida.
  • Messina JL; Department of Molecular Oncology, Moffitt Cancer Center and Research Institute, Tampa, Florida.
JAMA Dermatol ; 157(7): 831-835, 2021 Jul 01.
Article em En | MEDLINE | ID: mdl-33978681
ABSTRACT
IMPORTANCE Acral skin may develop nevi, but their mutational status and association with acral melanoma is unclear.

OBJECTIVE:

To perform targeted next-generation sequencing on a cohort of acral nevi to determine their mutational spectrum. DESIGN, SETTING, AND

PARTICIPANTS:

Acral nevi specimens (n = 50) that had been obtained for diagnostic purposes were identified from the pathology archives of a tertiary care academic cancer center and a university dermatology clinic. Next-generation sequencing was performed on DNA extracted from the specimens, and mutations called. A subset of samples was stained immunohistochemically for the BRAF V600E mutation.

RESULTS:

A total of 50 nevi from 49 patients (19 males and 30 females; median [range] age, 48 [13-85] years) were examined. Analysis of the sequencing data revealed a high prevalence of BRAF mutations (n = 43), with a lower frequency of NRAS mutations (n = 5). Mutations in BRAF and NRAS were mutually exclusive. CONCLUSIONS AND RELEVANCE In this cohort study, nevi arising on mostly sun-protected acral skin showed a rate of BRAF mutation similar to that of acquired nevi on sun-exposed skin but far higher than that of acral melanoma. These findings are in contrast to the well-characterized mutational landscape of acral melanoma.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Nevo Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Nevo Idioma: En Ano de publicação: 2021 Tipo de documento: Article