BRAF V600E Mutation in Malignant Melanoma—A Romanian Research Experience

Author:

Avădănei Elena-Roxana12,Căruntu Irina-Draga13,Nucă Irina24ORCID,Balan Raluca1ORCID,Lozneanu Ludmila15ORCID,Giusca Simona-Eliza1ORCID,Amalinei Cornelia16ORCID

Affiliation:

1. Department of Morpho-Functional Sciences I–Histology, Pathology, “Grigore T. Popa” University of Medicine and Pharmacy, 16 University Street, 700115 Iași, Romania

2. Praxis Medical Investigation Laboratory, 35 Moara de Vant Street, 700376 Iași, Romania

3. Romanian Medical Science Academy, 1 I.C. Bratianu Boulevard, 030171 Bucharest, Romania

4. Department of Mother and Child Medicine-Genetics, “Grigore T. Popa” University of Medicine and Pharmacy, 16 University Street, 700115 Iași, Romania

5. Department of Pathology, “Sf. Spiridon” Clinical Emergency County Hospital, 1 Independentei Street, 700111 Iași, Romania

6. Department of Histopathology, Institute of Legal Medicine, 4 Buna Vestire Street, 700455 Iași, Romania

Abstract

Background and Objectives: The most common mutation in malignant melanoma (MM) is the single-point mutation of v-raf murine sarcoma viral oncogene homolog B1 (BRAF) oncogene. Our study aims to evaluate BRAF V600E mutation, highlighting its frequency differences in primary versus metastatic MM. Materials and Methods: The study group comprised 133 patients diagnosed with MM in several county hospitals of the north-eastern region of Romania who have been assigned for investigation into BRAF V600E mutation in the private medical system. The material consisted of archived formalin-fixed paraffin-embedded (FFPE) blocks. BRAF V600E mutation was identified using the fully automated IdyllaTM BRAF mutation test system. Results: Out of the total of 133 cases, 78 cases were primary tumors, while 55 cases were metastatic MMs. Genetic analysis revealed the presence of BRAF V600E mutation in 66 cases (49.62%) and the wild-type genotype in 67 cases (50.37%). We found a statistically significant difference of the mutation frequency according to age (p = 0.0072). The mutated genotype was found in 45 cases out of 78 primary MMs (57.69%) and in 21 cases out of 55 secondary MMs (38.18%), with a statistically significant difference in favor of primary tumors (p = 0.0413). The correlations between the histopathological types, Clark’s level, Breslow index, ulceration, and lymphovascular invasion, respectively, and the mutated genotype were not statistically significant. BRAF V600E mutation was identified in 15 out of 40 secondary tumors with lymph node location (37.5%) and in 6 out of 15 secondary tumors with another location (40%) without statistically significant differences between the mutation frequency and the location of the secondary tumors. Conclusions: Our results support MM high genetic heterogeneity, pointing out the relationship between BRAF V600E mutation and several clinicopathological characteristics, in primary and metastatic MMs, stressing the importance of BRAF testing implementation in Romania.

Publisher

MDPI AG

Reference52 articles.

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3. Elder, D.E., Masii, R., Scolyer, R.A., and Willemze, R. (2018). WHO Classification of Skin Tumours, International Agency for Research on Cancer. [4th ed.].

4. The Cancer Genome Atlas Network (2015). Genomic classification of cutaneous melanoma. Cell, 161, 1681–1696.

5. Mutations of the BRAF gene in human cancer;Davies;Nature,2002

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