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. 2017 Nov 1;20(5):642–654. doi: 10.1093/neuonc/nox198

Table 1.

Summary of patient-derived GBM

GBM Cells In Vivo Phenotype Genetic Alteration CD44 PTEN p-Akt (Ser473) p-Akt
(Thr308)
MGMT Main Subtype TMZ IC50
(µM)
Invasiveness Pathological Feature Methylation Protein
MGG4 N Endothel. proliferation MYC# - + + + M Not clear 32
MGG6 I Conventional EGFR#, MDM4#, PI3KC2B#, CDKN2A&B- - NT + + + M Classical 36
MGG8 I PNET-like component MYCN#, MDM2#,
PDGFRA#, CDKN2A&B- -
+/- + + M PN 6
MGG18 N Giant cell NT ++ ++ ++ M MES 315
MGG23 I Gemistocytic CDKN2A&B- - ++ ++ + U + MES 355
MGG24 I Conventional EGFR# ++ + + + U/M + Classical 166
MGG29 N Oligo-like component NT −/+ + ++ + U Not clear >3000

Abbreviations: N, nodular; I, invasive; #, copy number amplifications; - -, homozygous deletion; PNET, primitive neuroectodermal tumor; PTEN, phosphatase and tensin homolog; +, positive; ++, strongly positive; −, negative; +/-, heterogeneous; M, methylated MGMT promoter; U, unmethylated MGMT promoter; U/M, a major unmethylated band with a weak methylated band; PN, proneural; MES, mesenchymal; NT, not tested.