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YB-1在髓母细胞瘤中表达升高,并驱动依赖于音猬因子的小脑颗粒神经元祖细胞和髓母细胞瘤细胞的增殖。

YB-1 is elevated in medulloblastoma and drives proliferation in Sonic hedgehog-dependent cerebellar granule neuron progenitor cells and medulloblastoma cells.

作者信息

Dey A, Robitaille M, Remke M, Maier C, Malhotra A, Gregorieff A, Wrana J L, Taylor M D, Angers S, Kenney A M

机构信息

Department of Pediatric Oncology, Emory University, Atlanta, GA, USA.

Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada.

出版信息

Oncogene. 2016 Aug 11;35(32):4256-68. doi: 10.1038/onc.2015.491. Epub 2016 Jan 4.

Abstract

Postnatal proliferation of cerebellar granule neuron precursors (CGNPs), proposed cells of origin for the SHH-associated subgroup of medulloblastoma, is driven by Sonic hedgehog (Shh) and insulin-like growth factor (IGF) in the developing cerebellum. Shh induces the oncogene Yes-associated protein (YAP), which drives IGF2 expression in CGNPs and mouse Shh-associated medulloblastomas. To determine how IGF2 expression is regulated downstream of YAP, we carried out an unbiased screen for transcriptional regulators bound to IGF2 promoters. We report that Y-box binding protein-1 (YB-1), an onco-protein regulating transcription and translation, binds to IGF2 promoter P3. We observed that YB-1 is upregulated across human medulloblastoma subclasses as well as in other varieties of pediatric brain tumors. Utilizing the cerebellar progenitor model for the Shh subgroup of medulloblastoma in mice, we show for the first time that YB-1 is induced by Shh in CGNPs. Its expression is YAP-dependent and it is required for IGF2 expression in CGNPs. Finally, both gain-of function and loss-of-function experiments reveal that YB-1 activity is required for sustaining CGNP and medulloblastoma cell (MBC) proliferation. Collectively, our findings describe a novel role for YB-1 in driving proliferation in the developing cerebellum and MBCs and they identify the SHH:YAP:YB1:IGF2 axis as a powerful target for therapeutic intervention in medulloblastomas.

摘要

小脑颗粒神经元前体细胞(CGNP)在出生后的增殖是髓母细胞瘤中与音猬因子(SHH)相关亚组的潜在起源细胞,在发育中的小脑中由音猬因子(Shh)和胰岛素样生长因子(IGF)驱动。Shh诱导原癌基因Yes相关蛋白(YAP),后者驱动CGNP和小鼠Shh相关髓母细胞瘤中IGF2的表达。为了确定YAP下游IGF2的表达是如何调控的,我们对与IGF2启动子结合的转录调节因子进行了无偏见筛选。我们报告Y盒结合蛋白1(YB-1),一种调节转录和翻译的癌蛋白,与IGF2启动子P3结合。我们观察到YB-1在人类髓母细胞瘤各亚类以及其他类型的儿童脑肿瘤中均上调。利用小鼠髓母细胞瘤Shh亚组的小脑祖细胞模型,我们首次表明Shh在CGNP中诱导YB-1。其表达依赖于YAP,且是CGNP中IGF2表达所必需的。最后,功能获得和功能丧失实验均表明,YB-1活性是维持CGNP和髓母细胞瘤细胞(MBC)增殖所必需的。总的来说,我们的研究结果描述了YB-1在驱动发育中的小脑和MBC增殖中的新作用,并确定了SHH:YAP:YB1:IGF2轴是髓母细胞瘤治疗干预的有力靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f4a/4931992/16c4b4368a47/nihms742077f1.jpg

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