Neuroblastoma and MYCN.

Neuroblastoma and MYCN.
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DOI:
10.1101/cshperspect.a014415
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发表时间:
2013-10-01
影响因子:
5.4
通讯作者:
Weiss WA
Weiss WA
中科院分区:
医学2区
文献类型:
--
作者:
Huang M;Weiss WA

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神经母细胞瘤是儿童最常见的颅外实体瘤,被认为起源于未分化的神经脊细胞。MYC家族成员MYCN的扩增在约25%的病例中被发现,并与高危疾病和不良预后相关。目前,MYCN扩增仍然是神经母细胞瘤风险的最具特征性的遗传标记。本文综述了MYCN在神经母细胞瘤中的作用,并重点介绍了最近发现的其他驱动基因突变。同时也对在蛋白质稳定性和转录水平上针对MYCN的策略进行了综述。
Neuroblastoma, the most common extracranial solid tumor of childhood, is thought to originate from undifferentiated neural crest cells. Amplification of the MYC family member, MYCN, is found in ~25% of cases and correlates with high-risk disease and poor prognosis. Currently, amplification of MYCN remains the best-characterized genetic marker of risk in neuroblastoma. This article reviews roles for MYCN in neuroblastoma and highlights recent identification of other driver mutations. Strategies to target MYCN at the level of protein stability and transcription are also reviewed.
DOI: 10.1196/annals.1322.017
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