作者: Michael B. Foote , Nickolas Papadopoulos , Luis A. Diaz
DOI: 10.1016/J.CCELL.2015.06.014
关键词: ATRX 、 Glioma 、 IDH1 、 Biology 、 Bioinformatics 、 Histopathology
摘要: Newly published studies validate prior reports that specific combinations of genetic alternations in IDH1/2, ATRX, TERT, TP53, and co-deletion 1p/19q have the ability to reclassify gliomas into rational subsets, defining a glioma's biological clinical behavior more accurately than stratifications based solely on histopathology.