Neill Stewart G, Saxe Debra F, Rossi Michael R, Schniederjan Matthew J, Brat Daniel J
From the Departments of Pathology and Laboratory Medicine (Drs Neill, Saxe, Rossi, Schniederjan, and Brat) and Radiation Oncology (Dr Rossi), Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia; and the Department of Pathology, Children's Healthcare of Atlanta, Atlanta, Georgia (Dr Schniederjan).
Arch Pathol Lab Med. 2017 Mar;141(3):355-365. doi: 10.5858/arpa.2016-0276-SAI.
The evaluation of central nervous system tumors increasingly relies on molecular genetic methods to aid in classification, offer prognostic information, and predict response to therapy. Available assays make it possible to assess genetic losses, amplifications, translocations, mutations, or the expression levels of specific gene transcripts or proteins. Current molecular diagnostics frequently use a panel-based approach and whole genome analysis, and generally rely either on DNA sequencing or on hybridization-based methodologies, such as those used in cytogenomic microarrays. In some cases, immunohistochemistry can be used as a surrogate for genetic analysis when the mutation of interest consistently results in overexpression or underexpression of a known protein product. In surgical neuropathology practice, the diagnostic workup of diffuse gliomas, medulloblastomas, low-grade circumscribed gliomas, as well as other diseases, now routinely incorporates the results of genomic studies. Here we summarize our institution's current approach to diagnostic surgical neuropathology, using these contemporary molecular diagnostic applications.
中枢神经系统肿瘤的评估越来越依赖分子遗传学方法来辅助分类、提供预后信息并预测治疗反应。现有的检测方法能够评估基因缺失、扩增、易位、突变,或特定基因转录本或蛋白质的表达水平。当前的分子诊断通常采用基于检测板的方法和全基因组分析,并且一般依赖于DNA测序或基于杂交的方法,如细胞基因组微阵列中使用的方法。在某些情况下,当感兴趣的突变始终导致已知蛋白质产物的过表达或低表达时,免疫组织化学可作为基因分析的替代方法。在外科神经病理学实践中,弥漫性胶质瘤、髓母细胞瘤、低级别局限性胶质瘤以及其他疾病的诊断检查现在通常会纳入基因组研究的结果。在此,我们使用这些当代分子诊断应用总结我们机构目前的诊断性外科神经病理学方法。