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BAP1功能丧失导致EZH2依赖性转化。

Loss of BAP1 function leads to EZH2-dependent transformation.

作者信息

LaFave Lindsay M, Béguelin Wendy, Koche Richard, Teater Matt, Spitzer Barbara, Chramiec Alan, Papalexi Efthymia, Keller Matthew D, Hricik Todd, Konstantinoff Katerina, Micol Jean-Baptiste, Durham Benjamin, Knutson Sarah K, Campbell John E, Blum Gil, Shi Xinxu, Doud Emma H, Krivtsov Andrei V, Chung Young Rock, Khodos Inna, de Stanchina Elisa, Ouerfelli Ouathek, Adusumilli Prasad S, Thomas Paul M, Kelleher Neil L, Luo Minkui, Keilhack Heike, Abdel-Wahab Omar, Melnick Ari, Armstrong Scott A, Levine Ross L

机构信息

Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Gerstner Sloan Kettering School of Biomedical Sciences, New York, New York, USA.

出版信息

Nat Med. 2015 Nov;21(11):1344-9. doi: 10.1038/nm.3947. Epub 2015 Oct 5.

Abstract

The tumor suppressors BAP1 and ASXL1 interact to form a polycomb deubiquitinase complex that removes monoubiquitin from histone H2A lysine 119 (H2AK119Ub). However, BAP1 and ASXL1 are mutated in distinct cancer types, consistent with independent roles in regulating epigenetic state and malignant transformation. Here we demonstrate that Bap1 loss in mice results in increased trimethylated histone H3 lysine 27 (H3K27me3), elevated enhancer of zeste 2 polycomb repressive complex 2 subunit (Ezh2) expression, and enhanced repression of polycomb repressive complex 2 (PRC2) targets. These findings contrast with the reduction in H3K27me3 levels seen with Asxl1 loss. Conditional deletion of Bap1 and Ezh2 in vivo abrogates the myeloid progenitor expansion induced by Bap1 loss alone. Loss of BAP1 results in a marked decrease in H4K20 monomethylation (H4K20me1). Consistent with a role for H4K20me1 in the transcriptional regulation of EZH2, expression of SETD8-the H4K20me1 methyltransferase-reduces EZH2 expression and abrogates the proliferation of BAP1-mutant cells. Furthermore, mesothelioma cells that lack BAP1 are sensitive to EZH2 pharmacologic inhibition, suggesting a novel therapeutic approach for BAP1-mutant malignancies.

摘要

肿瘤抑制因子BAP1和ASXL1相互作用形成一种多梳去泛素酶复合物,该复合物可去除组蛋白H2A赖氨酸119(H2AK119Ub)上的单泛素。然而,BAP1和ASXL1在不同的癌症类型中发生突变,这与它们在调节表观遗传状态和恶性转化中的独立作用一致。在这里,我们证明小鼠中Bap1的缺失会导致三甲基化组蛋白H3赖氨酸27(H3K27me3)增加、zeste 2多梳抑制复合物2亚基(Ezh2)表达升高以及多梳抑制复合物2(PRC2)靶标的抑制增强。这些发现与Asxl1缺失时H3K27me3水平的降低形成对比。体内条件性删除Bap1和Ezh2可消除仅由Bap1缺失诱导的髓系祖细胞扩增。BAP1的缺失导致H4K20单甲基化(H4K20me1)显著降低。与H4K20me1在EZH2转录调控中的作用一致,H4K20me1甲基转移酶SETD8的表达降低了EZH2的表达并消除了BAP1突变细胞的增殖。此外,缺乏BAP1的间皮瘤细胞对EZH2药物抑制敏感,这为BAP1突变恶性肿瘤提供了一种新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ffc/4636469/a81a569ff1b4/nihms717411f1.jpg

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