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神经母细胞瘤中与MYCN共同扩增的基因:沉默的伴随者还是表型的共同决定因素?

Genes co-amplified with MYCN in neuroblastoma: silent passengers or co-determinants of phenotype?

作者信息

Scott Debbie, Elsden Joanna, Pearson Andrew, Lunec John

机构信息

Cancer Research Unit, University of Newcastle Medical School, Framlington Place, Newcastle upon Tyne, NE2 4HH UK.

出版信息

Cancer Lett. 2003 Jul 18;197(1-2):81-6. doi: 10.1016/s0304-3835(03)00086-7.

Abstract

Amplification of the MYCN oncogene in neuroblastoma is associated with poor prognosis. The amplified unit of DNA can be up to 1 Mb in size and so could contain additional genes that affect tumour phenotype. Identification of such genes may assist in optimising the determination of prognosis, and could provide new targets for treatment. Three genes have so far been identified, which are frequently co-amplified with MYCN in neuroblastoma, DDX1, NAG and N-cym. In this review, the known or putative properties of the protein products of the genes are discussed, and their possible roles in determining tumour behaviour are assessed.

摘要

神经母细胞瘤中MYCN癌基因的扩增与预后不良相关。DNA的扩增单位大小可达1 Mb,因此可能包含影响肿瘤表型的其他基因。鉴定这些基因可能有助于优化预后判断,并可为治疗提供新靶点。迄今为止已鉴定出三个基因,它们在神经母细胞瘤中经常与MYCN共同扩增,即DDX1、NAG和N-cym。在本综述中,讨论了这些基因蛋白质产物的已知或推测特性,并评估了它们在决定肿瘤行为中的可能作用。

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