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. 2003 Aug;23(16):5540–5555. doi: 10.1128/MCB.23.16.5540-5555.2003

TABLE 1.

ΔNp73 cooperates with oncogenic Ras in promoting tumorigenicity in vivo

MEF type No. of mice with tumors/ total no. of mice No. of tumors/mouse Avg wt of tumor (g) Mean latency period (wk) ± SD
129 MEFsa
    GFP+K-RasV12 0/4 NAe NA NA
    ΔNp73+K-RasV12 3/5 1, 1, 2 1.75 10 ± 3
    ΔNp73+N-RasD12 2/2 1, 2 0.62 10 ± 3
    ΔNp73+H-RasV12 2/4 1, 2 0.53 4 ± 1
    p53 H175+K-RasV12 5/5 2, 2, 2, 2, 2 1.37 2.5
    p53 H175+N-RasD12 1/1 2 1.5 3
B6 MEFsb
    GFP+H-RasV12 0/4 NA NA NA
    ΔNp73+H-RasV12 2/4 1, 1 0.25 9 ± 2
    ΔNp73+K-RasV12 0/4 NA NA NA
    p53−/−+H-RasV12 2/2 2, 2 0.6 2.5
    p53 H175+H-RasV12 2/2 2, 2 0.6 2.5
Spontaneously immortalized ΔNp73 129 MEFsc
    +H-RasV12 (expt 1) 2/2 2, 2 0.45 1.4d
    +H-RasV12 (expt 2) 2/2 2, 2 0.52 1.4d
Passaged and in vitro-transformed 129 MEFs (ΔNp73+H-RasV12) 2/2 1, 1 0.7 4.5 ± 1
p73−/− MEFs (GFP+H-RasV12) 0/2 NA NA NA
a

MSCV based.

b

Percent Rpuro based, after selection.

c

Expt 1, two populations pooled, MSCV based; expt 2, three clones pooled, Rpuro based after selection.

d

That is, 10 days.

e

NA, not applicable.