神经母细胞瘤和神经嵴细胞ALK和GSK3的共同特征

Journal of Experimental Neuroscience Pub Date : 2018-08-13 eCollection Date: 2018-01-01 DOI:10.1177/1179069518792499
Sandra G Gonzalez Malagon, Karen J Liu
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引用次数: 6

摘要

神经母细胞瘤是最常见和最致命的儿童癌症之一。神经母细胞瘤起源于神经嵴系的转化细胞。该疾病的预后差异很大,从自发消退到侵袭性转移。虽然这种可变性可能反映了神经嵴细胞固有的迁移能力和多能性,但神经母细胞瘤和胚胎神经嵴细胞之间的直接比较很少,部分原因是哺乳动物神经嵴谱系在体内的可及性有限。我们最近的研究表明间变性淋巴瘤激酶(ALK)和糖原合成酶激酶3 (GSK3)之间存在新的联系。我们的研究表明,通过酪氨酸磷酸化对GSK3的alk依赖性调节可能会改变GSK3的底物特异性,从而调节迁移神经嵴细胞的细胞骨架动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

ALK and GSK3: Shared Features of Neuroblastoma and Neural Crest Cells.

ALK and GSK3: Shared Features of Neuroblastoma and Neural Crest Cells.

ALK and GSK3: Shared Features of Neuroblastoma and Neural Crest Cells.

Neuroblastoma is one of the most common and deadly childhood cancers. Neuroblastoma arises from transformed cells of the neural crest lineage. Outcomes of the disease vary greatly, ranging from spontaneous regression to aggressive metastases. While this variability may reflect the inherent migratory capabilities and multipotency of neural crest cells, there have been few direct comparisons between neuroblastoma and embryonic neural crest cells, in part because of the limited in vivo accessibility of the mammalian neural crest lineage. Our recent studies demonstrate a novel link between anaplastic lymphoma kinase (ALK) and glycogen synthase kinase 3 (GSK3). Our work suggests that ALK-dependent regulation of GSK3 via tyrosine phosphorylation may alter the substrate specificity of GSK3, thus regulating cytoskeletal dynamics in migrating neural crest cells.

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