Department of Neurological Surgery, Weill Cornell Medical College, New York, NY 10065, USA.
Lancet Oncol. 2013 Jan;14(1):e19-27. doi: 10.1016/S1470-2045(12)70577-6.
Glial tumours in children have distinct patterns of epigenetic alteration, chromosomal structure, and gene and protein expression that differentiate them from their histological counterparts in adults. Understanding paediatric gliomas at the molecular level provides important prognostic and therapeutic insights, such as which genetic alterations confer a favourable response to adjuvant therapy, or which signalling pathways might be amenable to specific molecularly targeted agents. For clinicians, the ultimate goal is to individualise therapeutic regimens on the basis of the molecular fingerprint of a particular tumour and the prognosis conferred by this profile. In this Review, we examine a series of studies of molecular and genomic analysis of glial tumours in children, and discuss the many clinical insights that these molecular features provide.
儿童胶质肿瘤具有独特的表观遗传改变、染色体结构以及基因和蛋白表达模式,与成人的组织学对应物不同。在分子水平上了解小儿脑肿瘤可为预后和治疗提供重要的见解,例如哪些遗传改变预示对辅助治疗有良好反应,或者哪些信号通路可能对特定的分子靶向药物敏感。对于临床医生来说,最终目标是根据特定肿瘤的分子指纹和该图谱所预示的预后来为治疗方案进行个体化。在这篇综述中,我们检查了一系列关于儿童胶质肿瘤的分子和基因组分析研究,并讨论了这些分子特征所提供的许多临床见解。