Program in Molecular Biology and Biotechnology, University of North Carolina School of Medicine, USA.
Brain Res Bull. 2012 May 1;88(1):72-9. doi: 10.1016/j.brainresbull.2011.06.002. Epub 2011 Jun 13.
Over the last decade, genetically engineered mouse models have been extensively used to dissect the genetic requirements for neoplastic initiation and progression of diffuse gliomas. While these models faithfully recapitulate the histopathological features of human gliomas, comparative genomic analyses are increasingly being utilized to comprehensively assess their fidelity to recently identified molecular subtypes of these tumors. Future progress with these models will rely on incorporating insights not only from oncogenomics studies of cancer, but also from the developmental neuroscience and stem cell biology fields to design accurate and experimentally tractable models for use in translational cancer research, particularly for experimental therapeutics studies of molecularly defined subtypes of gliomas.
在过去的十年中,基因工程小鼠模型被广泛用于解析弥漫性神经胶质瘤发生和进展的遗传要求。虽然这些模型忠实地再现了人类神经胶质瘤的组织病理学特征,但比较基因组分析越来越多地被用于全面评估它们与这些肿瘤最近确定的分子亚型的保真度。这些模型的未来进展将不仅依赖于癌症肿瘤基因组学研究的见解,还依赖于发育神经科学和干细胞生物学领域的见解,以设计用于转化癌症研究的准确和可实验的模型,特别是用于分子定义的神经胶质瘤亚型的实验治疗学研究。