Brandi G, Deserti M, Palloni A, Turchetti D, Zuntini R, Pedica F, Frega G, De Lorenzo S, Abbati F, Rizzo A, Di Marco M, Massari F, Tavolari S
Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola-Malpighi University Hospital, Bologna, Italy; Division of Oncology, S. Orsola-Malpighi University Hospital, Bologna, Italy.
Division of Oncology, S. Orsola-Malpighi University Hospital, Bologna, Italy.
Cancer Genet. 2020 Oct;248-249:57-62. doi: 10.1016/j.cancergen.2020.10.001. Epub 2020 Oct 11.
BRCA1 associated protein-1 (BAP1) germline mutations define a novel hereditary cancer syndrome, namely BAP1 tumor predisposition syndrome (BAP1-TPDS), characterized by an increased susceptibility to develop different cancer types, including mesothelioma, uveal and cutaneous melanoma, renal cell carcinoma, and basal cell and squamous cell carcinoma. Currently, the role of BAP1 germline mutations in intrahepatic cholangiocarcinoma (iCCA) pathogenesis is less known. Here we report the first clinical case of a female patient who developed an iCCA when she was 47-years-old and was found to carry a novel germline mutation at a splicing site of exon 4 in BAP1 gene (NM_004656.4: c.255_255+6del). An accurate anamnesis revealed the absence of risk factors linked to iCCA development, except for a low occupational exposure to asbestos. In tumor tissue, BAP1 sequencing, multiplex ligation-dependent probe amplification and immunoistochemistry showed the loss of heterozygosity and lack of nuclear expression, suggesting that BAP1 wild-type allele and functional protein were lost in cancer cells, in line with the classical two-hit model of tumor suppressor genes. Further studies are needed to confirm whether iCCA may be included into BAP1-TPDS cancer phenotypes and whether minimal asbestos exposure may facilitate the development of this malignancy in individuals carrying BAP1 germline mutations.
乳腺癌1号关联蛋白1(BAP1)种系突变定义了一种新型遗传性癌症综合征,即BAP1肿瘤易感性综合征(BAP1-TPDS),其特征是易患多种不同类型的癌症,包括间皮瘤、葡萄膜和皮肤黑色素瘤、肾细胞癌以及基底细胞癌和鳞状细胞癌。目前,BAP1种系突变在肝内胆管癌(iCCA)发病机制中的作用尚不清楚。在此,我们报告首例临床病例,一名47岁女性患者罹患iCCA,且被发现BAP1基因第4外显子剪接位点存在一种新的种系突变(NM_004656.4:c.255_255+6del)。详细的病史询问显示,除了低水平职业性接触石棉外,不存在与iCCA发生相关的危险因素。在肿瘤组织中,BAP1测序、多重连接依赖探针扩增和免疫组化显示杂合性缺失和核表达缺失,表明癌细胞中BAP1野生型等位基因和功能性蛋白缺失,这与肿瘤抑制基因的经典双打击模型一致。需要进一步研究来确认iCCA是否可纳入BAP1-TPDS癌症表型,以及最低限度的石棉接触是否会促进携带BAP1种系突变个体发生这种恶性肿瘤。