| Literature DB >> 27914687 |
Şule Öztürk Sari1, İsmaİl Yilmaz2, Orhun Çiğ Taşkin3, Gİzem Narli2, Fatma Şen4, Şenol Çomoğlu5, Pinar Firat3, Bİlge Bİlgİç3, Dİlek Yilmazbayhan3, Yasemİn Özlük3, Nesİmİ Büyükbabanİ3.
Abstract
Head and neck mucosal melanoma (HNMuM), which occurs mostly in the sinonasal and oral cavity, constitutes less than 1% of all malignant melanomas. Treatment options fail to improve the prognosis of this aggressive tumour that has low overall survival rates. Thus, development of new targeted therapies is essential. Unfortunately, limited data exist regarding their molecular profile. BRAF, NRAS, KIT, TERT and GNAQ/GNA11 oncogene mutations were investigated in 42 HNMuMs (28 sinonasal, 13 oral, 1 nasopharyngeal). Mutation rates were as follows: BRAF (4.8%), NRAS (4.8%), KIT (9.5%), TERT (7.5%), GNAQ/GNA11 (0%). Among 11 cases that harboured mutations (26%), 10 (91%) were located in sinonasal and one (9%) in the oral cavity. The literature was reviewed with comparison of frequencies based on the gathered data. NRAS and TERT promoter mutation rates were significantly higher in sinonasal than in oral location (p<0.05). Our results indicated that BRAF, NRAS, KIT, TERT and GNAQ/GNA11 gene mutations occur at low frequencies in HNMuMs, and subgroups (oral versus sinonasal) differ in their molecular profile. Low rates of aforementioned mutations and activation of oncogenes by pathways other than sun exposure support the distinctive nature of HNMuMs with regard to their cutaneous counterparts.Entities:
Keywords: BRAF; GNAQ/GNA11; KIT; Mucosal melanoma; NRAS; TERT; head and neck; mutation; oral melanoma; sinonasal melanoma
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Year: 2016 PMID: 27914687 DOI: 10.1016/j.pathol.2016.09.065
Source DB: PubMed Journal: Pathology ISSN: 0031-3025 Impact factor: 5.306