Abstract
The BAP1 gene has emerged as a major tumor suppressor mutated with various frequencies in numerous human malignancies, including uveal melanoma, malignant pleural mesothelioma, clear cell renal cell carcinoma, intrahepatic cholangiocarcinoma, hepatocellular carcinoma, and thymic epithelial tumors. BAP1 mutations are also observed at low frequency in other malignancies including breast, colorectal, pancreatic, and bladder cancers. BAP1 germline mutations are associated with high incidence of mesothelioma, uveal melanoma, and other cancers, defining the “BAP1 cancer syndrome.” Interestingly, germline BAP1 mutations constitute an important paradigm for gene–environment interactions, as loss of BAP1 predisposes to carcinogen-induced tumorigenesis. Inactivating mutations of BAP1 are also identified in sporadic cancers, denoting the importance of this gene for normal tissue homeostasis and tumor suppression, although some oncogenic properties have also been attributed to BAP1. BAP1 belongs to the deubiquitinase superfamily of enzymes, which are responsible for the maturation and turnover of ubiquitin as well as the reversal of substrate ubiquitination, thus regulating ubiquitin signaling. BAP1 is predominantly nuclear and interacts with several chromatin-associated factors, assembling multi-protein complexes with mutually exclusive partners. BAP1 exerts its function through highly regulated deubiquitination of its substrates. As such, BAP1 orchestrates chromatin-associated processes including gene expression, DNA replication, and DNA repair. BAP1 also exerts cytoplasmic functions, notably in regulating Ca2+ signaling at the endoplasmic reticulum. This DUB is also subjected to multiple post-translational modifications, notably phosphorylation and ubiquitination, indicating that several signaling pathways tightly regulate its function. Recent progress indicated that BAP1 plays essential roles in multiple cellular processes including cell proliferation and differentiation, cell metabolism, as well as cell survival and death. In this review, we summarize the biological and molecular functions of BAP1 and explain how the inactivation of this DUB might cause human cancers. We also highlight some of the unresolved questions and suggest potential new directions.
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Acknowledgements
This work was supported by grants from the Canadian Institutes of Health Research (2018–2023) to EBA. EBA is a senior scholar of the Fonds de la Recherche du Québec-Santé (FRQ-S). LM holds a PhD scholarship from the FRQ-S. AO holds PhD scholarships from the FRQ-S and the Cole Foundation. Certain forms and shapes displayed in figures were taken and modified from Servier Medical Art, licensed under a Creative Common Attribution 3.0 Generic License. http://smart.servier.com/.
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EBA, ML, AO, and BE collected the references and wrote the manuscript. ML, AO, BE, and EBA realized the illustration. BL, NL, and AN contributed to the general improvement of the writing and critical review of the figures.
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Masclef, L., Ahmed, O., Estavoyer, B. et al. Roles and mechanisms of BAP1 deubiquitinase in tumor suppression. Cell Death Differ 28, 606–625 (2021). https://doi.org/10.1038/s41418-020-00709-4
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DOI: https://doi.org/10.1038/s41418-020-00709-4
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