Wu Jianqiang, Keng Vincent W, Patmore Deanna M, Kendall Jed J, Patel Ami V, Jousma Edwin, Jessen Walter J, Choi Kwangmin, Tschida Barbara R, Silverstein Kevin A T, Fan Danhua, Schwartz Eric B, Fuchs James R, Zou Yuanshu, Kim Mi-Ok, Dombi Eva, Levy David E, Huang Gang, Cancelas Jose A, Stemmer-Rachamimov Anat O, Spinner Robert J, Largaespada David A, Ratner Nancy
Division of Experimental Hematology and Cancer Biology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital University of Cincinnati, Cincinnati, OH 45229, USA.
Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA; Department of Pediatrics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA; Center for Genome Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Cell Rep. 2016 Mar 1;14(8):1979-90. doi: 10.1016/j.celrep.2016.01.074. Epub 2016 Feb 18.
To identify genes and signaling pathways that initiate Neurofibromatosis type 1 (NF1) neurofibromas, we used unbiased insertional mutagenesis screening, mouse models, and molecular analyses. We mapped an Nf1-Stat3-Arid1b/β-catenin pathway that becomes active in the context of Nf1 loss. Genetic deletion of Stat3 in Schwann cell progenitors (SCPs) and Schwann cells (SCs) prevents neurofibroma formation, decreasing SCP self-renewal and β-catenin activity. β-catenin expression rescues effects of Stat3 loss in SCPs. Importantly, P-STAT3 and β-catenin expression correlate in human neurofibromas. Mechanistically, P-Stat3 represses Gsk3β and the SWI/SNF gene Arid1b to increase β-catenin. Knockdown of Arid1b or Gsk3β in Stat3(fl/fl);Nf1(fl/fl);DhhCre SCPs rescues neurofibroma formation after in vivo transplantation. Stat3 represses Arid1b through histone modification in a Brg1-dependent manner, indicating that epigenetic modification plays a role in early tumorigenesis. Our data map a neural tumorigenesis pathway and support testing JAK/STAT and Wnt/β-catenin pathway inhibitors in neurofibroma therapeutic trials.
为了鉴定引发1型神经纤维瘤病(NF1)神经纤维瘤的基因和信号通路,我们采用了无偏差插入诱变筛选、小鼠模型和分子分析方法。我们绘制了一条在Nf1缺失情况下被激活的Nf1-Stat3-Arid1b/β-连环蛋白信号通路。在雪旺细胞前体细胞(SCPs)和雪旺细胞(SCs)中对Stat3进行基因敲除可预防神经纤维瘤的形成,减少SCP的自我更新和β-连环蛋白活性。β-连环蛋白的表达可挽救Stat3缺失对SCPs的影响。重要的是,在人类神经纤维瘤中,p-STAT3和β-连环蛋白的表达呈正相关。从机制上讲,p-Stat3抑制Gsk3β和SWI/SNF基因Arid1b以增加β-连环蛋白。在Stat3(fl/fl);Nf1(fl/fl);DhhCre SCPs中敲低Arid1b或Gsk3β可挽救体内移植后的神经纤维瘤形成。Stat3通过以Brg1依赖的方式进行组蛋白修饰来抑制Arid1b,这表明表观遗传修饰在早期肿瘤发生中起作用。我们的数据绘制了一条神经肿瘤发生途径,并支持在神经纤维瘤治疗试验中测试JAK/STAT和Wnt/β-连环蛋白信号通路抑制剂。