Cole Yasemin C, Zhang Yu-Zhi, Gallo Beatrice, Januszewski Adam P, Nastase Anca, Essex David J, Thaung Caroline M H, Cohen Victoria M L, Sagoo Mandeep S, Bowcock Anne M
National Heart and Lung Institute, Imperial College London, London SW3 6LR, UK.
Department of Histopathology, Royal Brompton and Harefield NHS Foundation Trust, London SW3 6NP, UK.
Cancers (Basel). 2022 Aug 25;14(17):4105. doi: 10.3390/cancers14174105.
Uveal melanoma (UM) is an uncommon but highly aggressive ocular malignancy. Poor overall survival is associated with deleterious BAP1 alterations, which frequently occur with monosomy 3 (LOH3) and a characteristic gene expression profile. Tumor DNA from a cohort of 100 UM patients from Moorfields Biobank (UK) that had undergone enucleation were sequenced for known UM driver genes (BAP1, SF3B1, EIF1AX, GNAQ, and GNA11). Immunohistochemical staining of BAP1 and interphase FISH for chromosomes 3 and 8 was performed, and cellular localization of BAP1 was correlated with BAP1 mutations. Wildtype (WT) BAP1 staining was characterized by nBAP1 expression with <10% cytoplasmic BAP1 (cBAP1). Tumors exhibited heterogeneity with respect to BAP1 staining with different percentages of nBAP1 loss: ≥25% loss of nuclear BAP1 (nBAP1) was superior to chr8q and LOH3 as a prognostic indicator. Of the successfully sequenced UMs, 38% harbored oncogenic mutations in GNA11 and 48% harbored mutations in GNAQ at residues 209 or 183. Of the secondary drivers, 39% of mutations were in BAP1, 11% were in EIF1AX, and 20% were in the SF3B1 R625 hotspot. Most tumors with SF3B1 or EIF1AX mutations retained nuclear BAP1 (nBAP1). The majority of tumor samples with likely pathogenic BAP1 mutations, regardless of mutation class, displayed ≥25% loss of nBAP1. This included all tumors with truncating mutations and 80% of tumors with missense mutations. In addition, 60% of tumors with truncating mutations and 82% of tumors with missense mutations expressed >10% cBAP1.
葡萄膜黑色素瘤(UM)是一种罕见但极具侵袭性的眼部恶性肿瘤。总体生存率低与有害的BAP1改变有关,这种改变常与3号染色体单体性(LOH3)及特征性基因表达谱同时出现。对来自英国摩尔菲尔德生物样本库的100例接受眼球摘除术的UM患者队列的肿瘤DNA进行测序,检测已知的UM驱动基因(BAP1、SF3B1、EIF1AX、GNAQ和GNA11)。进行BAP1免疫组化染色及3号和8号染色体的间期荧光原位杂交(FISH),并将BAP1的细胞定位与BAP1突变相关联。野生型(WT)BAP1染色的特征是nBAP1表达且细胞质BAP1(cBAP1)<10%。肿瘤在BAP1染色方面表现出异质性,不同百分比的nBAP1缺失情况各异:核BAP1(nBAP1)缺失≥25%作为预后指标优于8号染色体长臂(chr8q)和LOH3。在成功测序的UM中,38%在GNA11中存在致癌突变,48%在GNAQ的第209位或183位残基处存在突变。在次要驱动基因中,39%的突变位于BAP1,11%位于EIF1AX,20%位于SF3B1的R625热点。大多数具有SF3B1或EIF1AX突变的肿瘤保留核BAP1(nBAP1)。大多数可能具有致病性BAP1突变的肿瘤样本,无论突变类型如何,均显示nBAP1缺失≥25%。这包括所有具有截短突变的肿瘤以及80%具有错义突变的肿瘤。此外,60%具有截短突变的肿瘤和82%具有错义突变的肿瘤表达>10%的cBAP1。