Departments of Surgery.
Pathology.
Melanoma Res. 2019 Jun;29(3):248-253. doi: 10.1097/CMR.0000000000000523.
Uveal melanoma is a rare form of melanoma and the most frequent primary eye malignancy in adults. The major molecular alterations underlying uveal melanoma pathogenesis affect mainly the GNAQ, GNA11, SF3B1, and BAP1 genes. In this study, we somatically genotyped 31 Brazilian uveal melanomas for BRAF, GNA11, GNAQ, SF3B1, and BAP1 gene mutations and assessed BRCA2 and p53 protein expression. GNAQ and GNA11 mutations were detected in 60%, and SF3B1 mutation rate was 30%. p53 Immunostaining was markedly positive in 5/31, and 3/31 samples showed negative BRCA2 expression. This study supports the importance of these key genes in uveal melanoma tumorigenesis; p53 and BRCA pathways seem to play a role in a subset of patients, possibly heralding unfavorable prognosis.
葡萄膜黑色素瘤是一种罕见的黑色素瘤,也是成年人中最常见的原发性眼部恶性肿瘤。葡萄膜黑色素瘤发病机制中的主要分子改变主要影响 GNAQ、GNA11、SF3B1 和 BAP1 基因。在这项研究中,我们对 31 例巴西葡萄膜黑色素瘤进行了 BRAF、GNA11、GNAQ、SF3B1 和 BAP1 基因突变的体细胞基因分型,并评估了 BRCA2 和 p53 蛋白的表达。60%检测到 GNAQ 和 GNA11 突变,SF3B1 突变率为 30%。31 例中有 5 例 p53 免疫染色明显阳性,3 例 BRCA2 表达阴性。这项研究支持这些关键基因在葡萄膜黑色素瘤发生中的重要性;p53 和 BRCA 途径似乎在一部分患者中发挥作用,可能预示着预后不良。