Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Cancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Cell Rep. 2022 Sep 20;40(12):111363. doi: 10.1016/j.celrep.2022.111363.
Loss-of-function mutations in the polycomb repressive complex 2 (PRC2) occur frequently in malignant peripheral nerve sheath tumor, an aggressive sarcoma that arises from NF1-deficient Schwann cells. To define the oncogenic mechanisms underlying PRC2 loss, we use engineered cells that dynamically reassemble a competent PRC2 coupled with single-cell sequencing from clinical samples. We discover a two-pronged oncogenic process: first, PRC2 loss leads to remodeling of the bivalent chromatin and enhancer landscape, causing the upregulation of developmentally regulated transcription factors that enforce a transcriptional circuit serving as the cell's core vulnerability. Second, PRC2 loss reduces type I interferon signaling and antigen presentation as downstream consequences of hyperactivated Ras and its cross talk with STAT/IRF transcription factors. Mapping of the transcriptional program of these PRC2-deficient tumor cells onto a constructed developmental trajectory of normal Schwann cells reveals that changes induced by PRC2 loss enforce a cellular profile characteristic of a primitive mesenchymal neural crest stem cell.
功能丧失性突变经常出现在恶性外周神经鞘瘤(MPNST)中,这种侵袭性肉瘤起源于 NF1 缺陷的雪旺细胞。为了明确 PRC2 缺失所涉及的致癌机制,我们使用工程细胞动态重建有功能的 PRC2,并结合临床样本的单细胞测序。我们发现了一个双重致癌过程:首先,PRC2 的缺失导致双价染色质和增强子景观的重塑,导致发育调节转录因子的上调,从而强制一个作为细胞核心脆弱性的转录回路。其次,PRC2 的缺失减少了 I 型干扰素信号和抗原呈递,这是由于 Ras 的过度激活及其与 STAT/IRF 转录因子的串扰的下游后果。将这些 PRC2 缺失肿瘤细胞的转录程序映射到构建的正常雪旺细胞发育轨迹上,揭示了 PRC2 缺失所诱导的变化强制了一个具有原始间充质神经嵴干细胞特征的细胞特征。