Exon 15 BRAF mutations are uncommon in melanomas arising in nonsun-exposed sites

被引:101
作者
Cohen, Y
Rosenbaum, E
Begum, S
Goldenberg, D
Esche, C
Lavie, O
Sidransky, D
Westra, WH
机构
[1] Johns Hopkins Med Inst, Dept Otolaryngol Head & Neck Surg, Div Head & Neck Canc Res, Baltimore, MD USA
[2] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD USA
[3] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
关键词
D O I
10.1158/1078-0432.CCR-03-0562
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: An activating point mutation of the BRAF oncogene has been identified in a high proportion of cutaneous nevi and cutaneous melanomas, but its frequency in melanomas arising from the mucosa of head and neck is unknown. Experimental Design: We tested 17 malignant mucosal melanomas of the head and neck for the thymine (T)-->adenine (A) missense mutation at nucleotide 1796 in the BRAF gene using direct sequencing and a newly developed assay that uses a novel primer extension method (Mutector assay). We also tested 21 cutaneous melanomas, including 13 arising from sun-exposed sites and 8 from a nonsun-exposed site, the vulvar skin. Results: The 1796T-->A mutation was detected in only 1 (6%) of the sinonasal melanomas. As for cutaneous melanomas, a BRAF mutation was detected in 8 (62%) of the tumors arising in sun-exposed sites but in none (0%) of vulvar melanomas. Conclusions: In contrast to cutaneous melanomas arising in sun-exposed sites, mucosal melanomas of the head and neck do not frequently harbor an activating; mutation of BRAF. This finding additionally supports the view that the various subtypes of melanoma are not equivalent and that distinct genetic alterations may underlie well recognized differences in risk factors and behavioral patterns. Accordingly, patients with melanomas should not tie collectively regarded as a uniform group as new strategies are developed that target specific genetic alterations.
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页码:3444 / 3447
页数:4
相关论文
共 25 条
  • [21] Mutations in BRAF and KRAS characterize the development of low-grade ovarian serous carcinoma
    Singer, G
    Oldt, R
    Cohen, Y
    Wang, BG
    Sidransky, D
    Kurman, RJ
    Shih, IM
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (06) : 484 - 486
  • [22] Mucosal melanomas
    Tomicic, J
    Wanebo, HJ
    [J]. SURGICAL CLINICS OF NORTH AMERICA, 2003, 83 (02) : 237 - +
  • [23] Distinct chromosomal aberrations in sinonasal mucosal melanoma as detected by comparative genomic hybridization
    van Dijk, M
    Sprenger, S
    Rombout, P
    Marres, H
    Kaanders, J
    Jeuken, J
    Ruiter, D
    [J]. GENES CHROMOSOMES & CANCER, 2003, 36 (02) : 151 - 158
  • [24] vanElsas A, 1996, AM J PATHOL, V149, P883
  • [25] PRESENCE OF MELANOCYTES IN NASAL CAVITY
    ZAK, FG
    LAWSON, W
    [J]. ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1974, 83 (04) : 515 - 519