Escoubet-Lozach Laure, Lin I-Lin, Jensen-Pergakes Kristen, Brady Helen A, Gandhi Anita K, Schafer Peter H, Muller George W, Worland Peter J, Chan Kyle W H, Verhelle Dominique
Celgene, San Diego, California 92121, USA.
Cancer Res. 2009 Sep 15;69(18):7347-56. doi: 10.1158/0008-5472.CAN-08-4898. Epub 2009 Sep 8.
Lenalidomide and pomalidomide have both been evaluated clinically for their properties as anticancer agents, with lenalidomide being available commercially. We previously reported that both compounds cause cell cycle arrest in Burkitt's lymphoma and multiple myeloma cell lines by increasing the level of p21(WAF-1) expression. In the present study, we unravel the molecular mechanism responsible for p21(WAF-1) up-regulation using Namalwa cells as a human lymphoma model. We show that the increase of p21(WAF-1) expression is regulated at the transcriptional level through a mechanism independent of p53. Using a combination of approaches, we show that several GC-rich binding transcription factors are involved in pomalidomide-mediated up-regulation of p21(WAF-1). Furthermore, we report that p21(WAF-1) up-regulation is associated with a switch from methylated to acetylated histone H3 on p21(WAF-1) promoter. Interestingly, lysine-specific demethylase-1 (LSD1) silencing reduced both pomalidomide and lenalidomide up-regulation of p21(WAF-1), suggesting that this histone demethylase is involved in the priming of the p21(WAF-1) promoter. Based on our findings, we propose a model in which pomalidomide and lenalidomide modify the chromatin structure of the p21(WAF-1) promoter through demethylation and acetylation of H3K9. This effect, mediated via LSD1, provides GC-rich binding transcription factors better access to DNA, followed by recruitment of RNA polymerase II and transcription activation. Taken together, our results provide new insights on the mechanism of action of pomalidomide and lenalidomide in the regulation of gene transcription, imply possible efficacy in p53 mutated and deleted cancer, and suggest new potential clinical uses as an epigenetic therapy.
来那度胺和泊马度胺均已作为抗癌药物进行了临床评估,来那度胺已上市销售。我们之前报道过,这两种化合物通过提高p21(WAF-1)的表达水平,导致伯基特淋巴瘤和多发性骨髓瘤细胞系的细胞周期停滞。在本研究中,我们以Namalwa细胞作为人淋巴瘤模型,揭示了p21(WAF-1)上调的分子机制。我们发现,p21(WAF-1)表达的增加是通过一种独立于p53的机制在转录水平上进行调控的。通过多种方法相结合,我们发现几个富含GC的结合转录因子参与了泊马度胺介导的p21(WAF-1)上调。此外,我们报道p21(WAF-1)上调与p21(WAF-1)启动子上组蛋白H3从甲基化转变为乙酰化有关。有趣的是,赖氨酸特异性去甲基化酶-1(LSD1)沉默降低了泊马度胺和来那度胺对p21(WAF-1)的上调作用,表明这种组蛋白去甲基化酶参与了p21(WAF-1)启动子的起始作用。基于我们的研究结果,我们提出了一个模型,其中泊马度胺和来那度胺通过H3K9的去甲基化和乙酰化修饰p21(WAF-1)启动子的染色质结构。这种由LSD1介导的效应使富含GC的结合转录因子能够更好地接近DNA,随后募集RNA聚合酶II并激活转录。综上所述,我们的结果为泊马度胺和来那度胺在基因转录调控中的作用机制提供了新的见解,暗示了在p53突变和缺失癌症中的可能疗效,并提示了作为表观遗传疗法的新潜在临床用途。