Wang Ami, Papneja Anjali, Hyrcza Martin, Al-Habeeb Ayman, Ghazarian Danny
Department of Laboratory Medicine and Pathobiology, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Department of Dermatology, University Health Network, University of Toronto, Toronto, Ontario, Canada.
J Clin Pathol. 2016 Sep;69(9):750-3. doi: 10.1136/jclinpath-2016-203866. Epub 2016 May 27.
The BAP1 gene (BRCA1-associated protein 1) is a tumour suppressor gene that encodes a deubiquitinating enzyme (DUB), regulating key cellular pathways, including cell cycle, cellular differentiation, transcription and DNA damage response. Germline BAP1 mutations cause a novel cancer syndrome characterised by early onset of multiple atypical Spitz tumours and increased risk of uveal and cutaneous melanoma, mesothelioma, renal cell carcinoma and various other malignancies. Recognising the clinicopathological features of specific BAP1-deficient tumours is crucial for early screening/tumour detection, with significant impact on patient outcome.
BAP1基因(BRCA1相关蛋白1)是一种肿瘤抑制基因,编码一种去泛素化酶(DUB),调节包括细胞周期、细胞分化、转录和DNA损伤反应在内的关键细胞途径。种系BAP1突变会导致一种新型癌症综合征,其特征是多种非典型斯皮茨瘤发病早,葡萄膜和皮肤黑色素瘤、间皮瘤、肾细胞癌及其他各种恶性肿瘤的风险增加。认识特定BAP1缺陷肿瘤的临床病理特征对于早期筛查/肿瘤检测至关重要,对患者预后有重大影响。