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首页> 外文期刊>Molecular oncology. >WT1 expression is inversely correlated with MYCN amplification or expression and associated with poor survival in non-MYCN-amplified neuroblastoma
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WT1 expression is inversely correlated with MYCN amplification or expression and associated with poor survival in non-MYCN-amplified neuroblastoma

机译:WT1的表达与MYCN扩增或表达呈负相关,并且与非MYCN扩增的神经母细胞瘤的生存不良相关

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摘要

Neuroblastoma (NB) is the most common extra cranial solid tumor in childhood and the most frequently diagnosed neoplasm during infancy. A striking feature of this tumor is its clinical heterogeneity. Several tumor progression markers have been delineated so far, among which MYCN amplification, which occurs in about 25% of total NB cases, with the percentage increasing to 30% in advanced stage NB. Although MYCN amplification is strongly correlated with NB of poor outcome, the MYCN status cannot alone predict all cases of poor survival in NB. Indeed NB without MYCN amplification (about 70-80% of NB) are not always favorable. WT1 was initially identified as a tumor suppressor gene involved in the development of a pediatric renal tumor (Wilms' tumor). Here, we describe an inverse correlation between WT1 expression and MYCN amplification and expression. However and most notably, our results show that WT1 gene expression is associated with a poor outcome for patients showing non-MYCN-amplified tumors. Thus WT1 expression is clinically significant in NB and may be a prognostic marker for better risk stratification and for an optimized therapeutic management of NB.
机译:神经母细胞瘤(NB)是儿童时期最常见的颅外实体瘤,也是婴儿期最常被诊断出的肿瘤。该肿瘤的显着特征是其临床异质性。迄今为止,已经划定了几种肿瘤进展标志物,其中MYCN扩增发生在全部NB病例的约25%中,在晚期NB中该百分比增加到30%。尽管MYCN扩增与不良结局的NB密切相关,但MYCN的状态不能单独预测所有NB生存不良的病例。实际上,没有MYCN扩增的NB(约占NB的70-80%)并不总是有利的。 WT1最初被鉴定为参与小儿肾肿瘤(Wilms肿瘤)发展的抑癌基因。在这里,我们描述了WT1表达与MYCN扩增和表达之间的逆相关性。然而,最值得注意的是,我们的结果表明,对于显示非MYCN扩增肿瘤的患者,WT1基因表达与不良预后相关。因此,WT1的表达在NB中具有临床意义,并且可能是更好的风险分层和NB的最佳治疗管理的预后标志物。

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