Piunti Andrea, Hashizume Rintaro, Morgan Marc A, Bartom Elizabeth T, Horbinski Craig M, Marshall Stacy A, Rendleman Emily J, Ma Quanhong, Takahashi Yoh-Hei, Woodfin Ashley R, Misharin Alexander V, Abshiru Nebiyu A, Lulla Rishi R, Saratsis Amanda M, Kelleher Neil L, James C David, Shilatifard Ali
Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Nat Med. 2017 Apr;23(4):493-500. doi: 10.1038/nm.4296. Epub 2017 Feb 27.
Diffuse intrinsic pontine glioma (DIPG) is a highly aggressive pediatric brainstem tumor characterized by rapid and uniform patient demise. A heterozygous point mutation of histone H3 occurs in more than 80% of these tumors and results in a lysine-to-methionine substitution (H3K27M). Expression of this histone mutant is accompanied by a reduction in the levels of polycomb repressive complex 2 (PRC2)-mediated H3K27 trimethylation (H3K27me3), and this is hypothesized to be a driving event of DIPG oncogenesis. Despite a major loss of H3K27me3, PRC2 activity is still detected in DIPG cells positive for H3K27M. To investigate the functional roles of H3K27M and PRC2 in DIPG pathogenesis, we profiled the epigenome of H3K27M-mutant DIPG cells and found that H3K27M associates with increased H3K27 acetylation (H3K27ac). In accordance with previous biochemical data, the majority of the heterotypic H3K27M-K27ac nucleosomes colocalize with bromodomain proteins at the loci of actively transcribed genes, whereas PRC2 is excluded from these regions; this suggests that H3K27M does not sequester PRC2 on chromatin. Residual PRC2 activity is required to maintain DIPG proliferative potential, by repressing neuronal differentiation and function. Finally, to examine the therapeutic potential of blocking the recruitment of bromodomain proteins by heterotypic H3K27M-K27ac nucleosomes in DIPG cells, we performed treatments in vivo with BET bromodomain inhibitors and demonstrate that they efficiently inhibit tumor progression, thus identifying this class of compounds as potential therapeutics in DIPG.
弥漫性脑桥内在型胶质瘤(DIPG)是一种侵袭性很强的儿童脑干肿瘤,其特征是患者迅速且一致地死亡。超过80%的这类肿瘤发生组蛋白H3的杂合点突变,导致赖氨酸到甲硫氨酸的替换(H3K27M)。这种组蛋白突变体的表达伴随着多梳抑制复合物2(PRC2)介导的H3K27三甲基化(H3K27me3)水平的降低,据推测这是DIPG肿瘤发生的驱动事件。尽管H3K27me3大量缺失,但在H3K27M阳性的DIPG细胞中仍能检测到PRC2活性。为了研究H3K27M和PRC2在DIPG发病机制中的功能作用,我们分析了H3K27M突变的DIPG细胞的表观基因组,发现H3K27M与H3K27乙酰化(H3K27ac)增加有关。与之前的生化数据一致,大多数异型H3K27M-K27ac核小体在活跃转录基因的位点与溴结构域蛋白共定位,而PRC2被排除在这些区域之外;这表明H3K27M不会将PRC2隔离在染色质上。残余的PRC2活性通过抑制神经元分化和功能来维持DIPG的增殖潜能。最后,为了检测阻断异型H3K27M-K27ac核小体在DIPG细胞中招募溴结构域蛋白的治疗潜力,我们在体内用BET溴结构域抑制剂进行了治疗,并证明它们能有效抑制肿瘤进展,从而确定这类化合物是DIPG的潜在治疗药物。