Table 1.
First Author, Year | Molecular Subtypes | Typical Genomic Profile | Enriched for MG | Main Histotypes | Prognosis |
---|---|---|---|---|---|
Radovich M et al. 2018 | 1 (B-like) | wtGTF2I, wtRAS, ↓p53, ↑MYC/MAX, ↓PPARA-RXRA, ↓XBP1-2, ↑MYB | + | B | Intermediate |
2 (C-like) | wtGTF2I, wtRAS, chr16q loss, ↓p53, ↑MYC/MAX, ↓XBP1-2, ↓PPARA-RXRA, ↑MYB | ₋ | C | Poor | |
3 (AB-like) | mGTF2I, wtRAS, ↑C19MC, ↑MYB, ↓p53, ↑FOXM1, ↓TAp73a, ↑E2F1/DP | ₋ | AB | Good | |
4 (A-like) | mGTF2I, mRAS, ↑C19MC, ↑p53, ↑XBP1-2, ↓MYC/MAX, ↓MYB, ↓FOXM1 | ₋ | A and AB | Good | |
Lee HS et al. 2017 | GTF2I | mGTF2I | ₋ | A and AB | Good |
TS | wtGTF2I, ↑genes associated with TS | ± | AB, B1 and B2 | Good | |
CS | wtGTF2I, sCNA low | + | B2 | Poor | |
CIN | wtGTF2I, sCNA high, delCDKN2A | + | B2, B3 and C | Poor |
Abbreviations: MG, myasthenia gravis; m, mutated; wt, wild-type; ↑, overexpressed; ↓, underexpressed; chr, chromosome; TS, T-cell signaling; CS, chromosomal stability; CIN, chromosomal instability; sCNA, somatic copy number alterations; del, deletion.