World-Class Research Center "Digital Biodesign and Personalized Healthcare", Sechenov First Moscow State Medical University, 119048 Moscow, Russia.
Multidisciplinary Medical Center, Group of Clinics, 194044 Saint-Petersburg, Russia.
Int J Mol Sci. 2022 Dec 21;24(1):157. doi: 10.3390/ijms24010157.
In 2021, the fifth edition of the WHO classification of tumors of the central nervous system (WHO CNS5) was published. Molecular features of tumors were directly incorporated into the diagnostic decision tree, thus affecting both the typing and staging of the tumor. It has changed the traditional approach, based solely on histopathological classification. The Cancer Genome Atlas project (TCGA) is one of the main sources of molecular information about gliomas, including clinically annotated transcriptomic and genomic profiles. Although TCGA itself has played a pivotal role in developing the WHO CNS5 classification, its proprietary databases still retain outdated diagnoses which frequently appear incorrect and misleading according to the WHO CNS5 standards. We aimed to define the up-to-date annotations for gliomas from TCGA's database that other scientists can use in their research. Based on WHO CNS5 guidelines, we developed an algorithm for the reclassification of TCGA glioma samples by molecular features. We updated tumor type and diagnosis for 828 out of a total of 1122 TCGA glioma cases, after which available transcriptomic and methylation data showed clustering features more consistent with the updated grouping. We also observed better stratification by overall survival for the updated diagnoses, yet WHO grade 3 -mutant oligodendrogliomas and astrocytomas are still indistinguishable. We also detected altered performance in the previous diagnostic transcriptomic molecular biomarkers (expression of , and genes and FREM2 molecular pathway) and prognostic gene signature (, , , and ) after reclassification. Thus, we conclude that further efforts are needed to reconsider glioma molecular biomarkers.
2021 年,世界卫生组织(WHO)中枢神经系统肿瘤分类第五版(WHO CNS5)发布。肿瘤的分子特征直接纳入诊断决策树,从而影响肿瘤的分型和分期。这改变了传统的仅基于组织病理学分类的方法。癌症基因组图谱(TCGA)是胶质瘤分子信息的主要来源之一,包括临床注释的转录组学和基因组图谱。尽管 TCGA 本身在开发 WHO CNS5 分类中发挥了关键作用,但它的专有数据库仍然保留了过时的诊断,这些诊断根据 WHO CNS5 标准经常显得不正确和具有误导性。我们的目的是确定 TCGA 数据库中最新的胶质瘤注释,以便其他科学家在研究中使用。基于 WHO CNS5 指南,我们开发了一种基于分子特征对 TCGA 胶质瘤样本进行重新分类的算法。在总共 1122 例 TCGA 胶质瘤病例中,我们对 828 例病例进行了肿瘤类型和诊断的更新,之后可用的转录组和甲基化数据显示出与更新分组更一致的聚类特征。我们还观察到更新后的诊断在总生存期方面的分层更好,但 WHO 分级 3-突变少突胶质细胞瘤和星形细胞瘤仍无法区分。我们还发现,在重新分类后,以前的诊断转录组分子生物标志物(表达基因和基因以及 FREM2 分子途径)和预后基因特征(、、、和)的性能发生了改变。因此,我们得出结论,需要进一步努力重新考虑胶质瘤分子生物标志物。