Au Sandy Leung-Kuen, Wong Carmen Chak-Lui, Lee Joyce Man-Fong, Wong Chun-Ming, Ng Irene Oi-Lin
State Key Laboratory for Liver Research and Department of Pathology, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong, People's Republic of China.
PLoS One. 2013 Jun 27;8(6):e68226. doi: 10.1371/journal.pone.0068226. Print 2013.
Enhancer of zeste homolog 2 (EZH2), the histone methyltransferase of the Polycomb Repressive complex 2 catalyzing histone H3 lysine 27 tri-methylation (H3K27me3), is frequently up-regulated in human cancers. In this study, we identified the tumor suppressor Deleted in liver cancer 1 (DLC1) as a target of repression by EZH2-mediated H3K27me3. DLC1 is a GTPase-activating protein for Rho family proteins. Inactivation of DLC1 results in hyper-activated Rho/ROCK signaling and is implicated in actin cytoskeleton reorganization to promote cancer metastasis. By chromatin immunoprecipitation assay, we demonstrated that H3K27me3 was significantly enriched at the DLC1 promoter region of a DLC1-nonexpressing HCC cell line, MHCC97L. Depletion of EZH2 in MHCC97L by shRNA reduced H3K27me3 level at DLC1 promoter and induced DLC1 gene re-expression. Conversely, transient overexpression of GFP-EZH2 in DLC1-expressing Huh7 cells reduced DLC1 mRNA level with a concomitant enrichment of EZH2 on DLC1 promoter. An inverse relation between EZH2 and DLC1 expression was observed in the liver, lung, breast, prostate, and ovarian cancer tissues. Treating cancer cells with the EZH2 small molecular inhibitor, 3-Deazaneplanocin A (DZNep), restored DLC1 expression in different cancer cell lines, indicating that EZH2-mediated H3K27me3 epigenetic regulation of DLC1 was a common mechanism in human cancers. Importantly, we found that DZNep treatment inhibited HCC cell migration through disrupting actin cytoskeleton network, suggesting the therapeutic potential of DZNep in targeting cancer metastasis. Taken together, our study has shed mechanistic insight into EZH2-H3K27me3 epigenetic repression of DLC1 and advocated the significant pro-metastatic role of EZH2 via repressing tumor and metastasis suppressors.
zeste 同源物 2 增强子(EZH2)是多梳抑制复合物 2 的组蛋白甲基转移酶,催化组蛋白 H3 赖氨酸 27 三甲基化(H3K27me3),在人类癌症中经常上调。在本研究中,我们确定肝癌缺失 1(DLC1)肿瘤抑制因子是 EZH2 介导的 H3K27me3 抑制的靶点。DLC1 是 Rho 家族蛋白的 GTP 酶激活蛋白。DLC1 的失活导致 Rho/ROCK 信号过度激活,并与肌动蛋白细胞骨架重组有关,从而促进癌症转移。通过染色质免疫沉淀分析,我们证明在不表达 DLC1 的肝癌细胞系 MHCC97L 的 DLC1 启动子区域,H3K27me3 显著富集。通过 shRNA 在 MHCC97L 中耗尽 EZH2 可降低 DLC1 启动子处的 H3K27me3 水平并诱导 DLC1 基因重新表达。相反,在表达 DLC1 的 Huh7 细胞中瞬时过表达 GFP-EZH2 可降低 DLC1 mRNA 水平,同时 EZH2 在 DLC1 启动子上富集。在肝癌、肺癌、乳腺癌、前列腺癌和卵巢癌组织中观察到 EZH2 和 DLC1 表达之间呈负相关。用 EZH2 小分子抑制剂 3-去氮杂胞苷(DZNep)处理癌细胞可恢复不同癌细胞系中 DLC1 的表达,表明 EZH2 介导的 DLC1 的 H3K27me3 表观遗传调控是人类癌症中的常见机制。重要的是,我们发现 DZNep 处理通过破坏肌动蛋白细胞骨架网络抑制肝癌细胞迁移,提示 DZNep 在靶向癌症转移方面的治疗潜力。总之,我们的研究揭示了 EZH2-H3K27me3 对 DLC1 的表观遗传抑制机制,并倡导 EZH2 通过抑制肿瘤和转移抑制因子在促进转移中发挥重要作用。