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. 2008 Dec 3;19(1):132–143. doi: 10.1111/j.1750-3639.2008.00234.x

Table 2.

Murine models of medulloblastoma shown with underlying genetics, mechanism of engineering and incidence. Abbreviations: TG = transgenic, KO = knockout.

Genetics Mechanism Incidence Reference
Ptch+/− Conventional KO 14%–19% by 10 months 23, 44, 98
Ptch+/− Conventional KO; irradiation 100% by 10 months 54, 55
Ptch+/−; p53−/− Conventional KO 100% by 2–3 months (89)
Ptch+/−; Ptch2±/− Conventional KO 17% by 10 months (44)
Ptch+/− Conditional KO (GFAP‐Cre, Math1‐Cre) 100% by 1–3 months (95)
ND2‐SmoA1 TG 94% by 2 months 26, 28
SmoM2 Conditional TG (GFAP‐Cre, Math1‐Cre, Olig2‐Cre, Tlx‐Cre) 100% by 2–4 months* (69)
Sufu+/−; p53−/− Conventional KO 58% by 10 months (42)
Shh RCAS 9%–34% by 3 months 7, 49, 60, 61
Shh; c‐myc/Akt/IGF2 RCAS 23%–48% by 3 months 60, 61
Shh; n‐myc RCAS 78% by 3 months (7)
Shh; Bcl‐2 RCAS 78% by 3 months (49)
Rb±/−; p53−/− Conditional KO (GFAP‐Cre) 25%–100% by 2–7 months (48)
Ink4c±/−; p53±/− Conventional and conditional KO (Nestin‐Cre); irradiation 20%–100% by 5 months (81)
Ptch+/−; Ink4c±/− Conventional KO 40%–50% by 9 months (81)
Lig4−/−; p53−/− Conventional KO 100% by 2 months (43)
Brca2−/−; p53±/− Conventional and conditional KO (Nestin‐Cre) 72%–83% by 4–8 months (17)
Xrcc4−/−; p53−/− Conventional and conditional KO (Nestin‐Cre) 100% by 6 months (94)
*

Estimated from reported average latency.