BRAF, KIT, and NRAS Mutations of Acral Melanoma in White Patients.


Journal

American journal of clinical pathology
ISSN: 1943-7722
Titre abrégé: Am J Clin Pathol
Pays: England
ID NLM: 0370470

Informations de publication

Date de publication:
15 04 2020
Historique:
pubmed: 6 2 2020
medline: 30 7 2020
entrez: 5 2 2020
Statut: ppublish

Résumé

Malignant acral melanoma (AM) is relatively infrequent in white patients. Molecular investigations have returned variable results regarding the mutational pattern. We sought to describe the mutation profile and clinicopathologic features of AM. We investigated BRAF, KIT, and NRAS mutational status in a series of 31 AM samples from white patients. Nodular melanoma was the most common histopathologic subtype (48.4%), followed by acral lentiginous melanoma (25.8%) and superficial spreading melanoma (25.8%). BRAF, KIT, and NRAS mutational rates were 12.9%, 17.2%, and 30.0%, respectively. We observed significant associations between KIT mutational status and a thinner Breslow thickness compared with wild-type (WT) status (P = .002), NRAS mutation status and younger age compared with WT. In patients presenting at least one mutation, triple-WT patients presented metastases most frequently. Although these data represent preliminary results, better knowledge of tumor biology and prognosis of AM can support the clinical approach and follow-up.

Identifiants

pubmed: 32017841
pii: 5722364
doi: 10.1093/ajcp/aqz209
doi:

Substances chimiques

Membrane Proteins 0
KIT protein, human EC 2.7.10.1
Proto-Oncogene Proteins c-kit EC 2.7.10.1
BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1
GTP Phosphohydrolases EC 3.6.1.-
NRAS protein, human EC 3.6.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

664-671

Informations de copyright

© American Society for Clinical Pathology, 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Emi Dika (E)

Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Giulia Veronesi (G)

Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Annalisa Altimari (A)

Laboratory of Oncologic and Transplantation Molecular Pathology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Mattia Riefolo (M)

Laboratory of Oncologic and Transplantation Molecular Pathology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Giulia Maria Ravaioli (GM)

Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Bianca Maria Piraccini (BM)

Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Martina Lambertini (M)

Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Elena Campione (E)

Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy.

Elisa Gruppioni (E)

Laboratory of Oncologic and Transplantation Molecular Pathology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Michelangelo Fiorentino (M)

Laboratory of Oncologic and Transplantation Molecular Pathology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

Barbara Melotti (B)

Medical Oncology Unit, Sant'Orsola Malpighi Hospital, Bologna, Italy.

Manuela Ferracin (M)

Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.

Annalisa Patrizi (A)

Dermatology, Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Italy.

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Classifications MeSH