Authors' Affiliations: Molecular and Cellular Biology Program, University of Washington; Clinical Research Division, Human Biology Division, and Public Health Sciences Division, Fred Hutchinson Cancer Research Center; Presage Biosciences; Sage Bionetworks; Seattle Children's Hospital, Seattle, Washington; Arthur and Sonia Labatt Brain Tumor Research Center and Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
Cancer Res. 2013 Nov 15;73(22):6828-37. doi: 10.1158/0008-5472.CAN-13-0730-T. Epub 2013 Oct 3.
While medulloblastoma, a pediatric tumor of the cerebellum, is characterized by aberrations in developmental pathways, the majority of genetic determinants remain unknown. An unbiased Sleeping Beauty transposon screen revealed MyoD as a putative medulloblastoma tumor suppressor. This was unexpected, as MyoD is a muscle differentiation factor and not previously known to be expressed in cerebellum or medulloblastoma. In response to deletion of one allele of MyoD, two other Sonic hedgehog-driven mouse medulloblastoma models showed accelerated tumor formation and death, confirming MyoD as a tumor suppressor in these models. In normal cerebellum, MyoD was expressed in the proliferating granule neuron progenitors that are thought to be precursors to medulloblastoma. Similar to some other tumor suppressors that are induced in cancer, MyoD was expressed in proliferating medulloblastoma cells in three mouse models and in human medulloblastoma cases. This suggests that although expression of MyoD in a proliferating tumor is insufficient to prevent tumor progression, its expression in the cerebellum hinders medulloblastoma genesis.
虽然髓母细胞瘤是一种小脑的小儿肿瘤,其特征在于发育途径的异常,但大多数遗传决定因素仍然未知。一项无偏的 Sleeping Beauty 转座子筛选发现 MyoD 是一种推定的髓母细胞瘤肿瘤抑制因子。这令人意外,因为 MyoD 是一种肌肉分化因子,以前不知道在小脑或髓母细胞瘤中表达。在 MyoD 的一个等位基因缺失的情况下,另外两种 Sonic hedgehog 驱动的小鼠髓母细胞瘤模型显示出加速的肿瘤形成和死亡,证实了 MyoD 在这些模型中是一种肿瘤抑制因子。在正常小脑中,MyoD 表达在增殖的颗粒神经元祖细胞中,这些细胞被认为是髓母细胞瘤的前体。与一些在癌症中诱导表达的其他肿瘤抑制因子类似,MyoD 在三种小鼠模型和人类髓母细胞瘤病例中的增殖性髓母细胞瘤细胞中表达。这表明,尽管 MyoD 在增殖性肿瘤中的表达不足以阻止肿瘤进展,但它在小脑中的表达阻碍了髓母细胞瘤的发生。