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首页> 外文期刊>Oncogene >The gene encoding the prostatic tumor suppressor PSP94 is a target for repression by the Polycomb group protein EZH2
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The gene encoding the prostatic tumor suppressor PSP94 is a target for repression by the Polycomb group protein EZH2

机译:编码前列腺肿瘤抑制因子PSP94的基因是被Polycomb组蛋白EZH2抑制的靶标

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PSP94, for prostatic secretory protein of 94 amino acids, is secreted by the prostate gland and functions as a suppressor of tumor growth and metastasis. The expression of PSP94 is lost in advanced, hormone-refractory prostate cancer and this correlates with an increased expression of the Polycomb protein EZH2 (enhancer of zeste homolog 2), which represses transcription via trimethylation of histone H3 on Lys27 (H3K27). We show here that these events are causally related and that the MSMB gene, which encodes PSP94, is trimethylated on H3K27 in androgen-refractory, but not in androgen-sensitive prostate cancer cells. Chromatin immunoprecipitation experiments confirmed an association of EZH2 with the MSMB gene. The RNAi-mediated knockdown of EZH2 resulted in a loss of H3K27 trimethylation and an increased expression of the MSMB gene. Conversely, the overexpression of EZH2 was associated with a decreased expression of the MSMB gene. We also demonstrate that MSMB is additionally repressed in androgen-refractory prostate cancer cells by the hypoacetylation of histone H3K9 and the hypermethylation of a CpG island in the promoter region. Our data disclose a hitherto unexplored link between the putative oncogene EZH2 and the tumor suppressor PSP94, and show that MSMB is silenced by EZH2 in advanced prostate cancer cells.
机译:PSP94是前列腺素分泌的94个氨基酸的前列腺分泌蛋白,具有抑制肿瘤生长和转移的作用。 PSP94的表达在晚期激素抵抗性前列腺癌中丢失,并且与Polycomb蛋白EZH2(zeste同源物2的增强子)的表达增加有关,后者通过Lys27(H3K27)上组蛋白H3的三甲基化来抑制转录。我们在这里显示这些事件是因果相关的,并且编码PSP94的MSMB基因在雄激素难治性的H3K27上被三甲基化,但是在雄激素敏感的前列腺癌细胞中却没有。染色质免疫沉淀实验证实了EZH2与MSMB基因的关联。 RNAi介导的EZH2敲低导致H3K27三甲基化损失和MSMB基因表达增加。相反,EZH2的过表达与MSMB基因表达降低有关。我们还证明,MSMB还通过组蛋白H3K9的低乙酰化和启动子区域CpG岛的超甲基化而在雄激素难治性前列腺癌细胞中被阻遏。我们的数据揭示了推定的致癌基因EZH2和抑癌基因PSP94之间迄今尚未探索的联系,并显示MSZH在晚期前列腺癌细胞中被EZH2沉默。

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