BAP1: Not just a BRCA1-associated protein.
BAP1: Not just a BRCA1-associated protein.
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BAP1:不仅是与BRCA1相关的蛋白质。
DOI:
10.1016/j.ctrv.2020.102091
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发表时间:
2020-11
影响因子:
11.8
通讯作者:
Kurzrock R
中科院分区:
文献类型:
--
作者:
Louie BH;Kurzrock R
BRCA1-Associated Protein 1 (BAP1) is a ubiquitin carboxy-terminal hydrolase that has been established as a tumor suppressor, utilizing its deubiquitinating activity to regulate a number of processes including DNA damage repair, cell cycle control, chromatin modification, programmed cell death, and the immune response. Mutations in the BAP1 gene commonly result in a number of aggressive cancers; predominantly uveal melanoma, malignant mesothelioma, renal cell carcinoma, and cutaneous melanoma. Importantly, germline mutations in the BAP1 gene have been established as a novel tumor predisposition syndrome, conferring an increased risk of hereditary, early-onset cancers. Current treatment options for cancers with BAP1 alterations are limited to standard therapies. However, several therapeutic avenues have been proposed to specifically target BAP1 alterations in cancer. Molecularly targeted approaches include histone deacetylase inhibitors and EZH2 inhibitors to target the role of BAP1 in chromatin modification and transcriptional regulation, respectively. PARP inhibitors and platinum chemotherapy agents have the potential to target BAP1-altered tumors, due to the role of BAP1 in DNA damage repair. Lastly, emerging reports suggest that BAP1-alterations in cancer confer distinct immunogenic phenotypes that may be particularly susceptible to novel cancer immunotherapies. This review aims to present a concise and up to date report on the BAP1 gene in cancer, surveying its functional roles, characteristics and clinical manifestations. Furthermore, we highlight the established and emerging therapeutic options for BAP1-mutated cancers.
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DOI:
10.1126/science.1194472
发表时间:
2010-12-03
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Harbour JW;Onken MD;Roberson ED;Duan S;Cao L;Worley LA;Council ML;Matatall KA;Helms C;Bowcock AM
通讯作者:
Bowcock AM
DOI:
10.2147/opth.s89591
发表时间:
2017
期刊:
Clinical ophthalmology (Auckland, N.Z.)
影响因子:
--
作者:
Krantz BA;Dave N;Komatsubara KM;Marr BP;Carvajal RD
通讯作者:
Carvajal RD
影响因子:
10.9
作者:
Heppt, Markus, V;Amaral, Teresa;Berking, Carola
通讯作者:
Berking, Carola
影响因子:
8.1
作者:
Gupta, Mrinali P.;Lane, Anne Marie;Kim, Ivana K.
通讯作者:
Kim, Ivana K.
影响因子:
13.8
作者:
Garfield, Erin M.;Walton, Kara E.;Gerami, Pedram
通讯作者:
Gerami, Pedram