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. 2016 Feb 7;7(7):7403–7414. doi: 10.18632/oncotarget.7232

Table 1. MPNST development in Nf1 mutant mice following p53 knockdown.

Mouse genotype (injection) Hyperplasia MPNST MPNST latency, mean days (range)
Periostin-Cre; Nf1flox/flox (vehicle) 2/11 0/11 No tumors: 83-304d*
Periostin-Cre; Nf1flox/flox (pTomo-shNf1;shp53) 8/18 10/18 183d (144-278d)
GFAP-Cre; Nf1flox/null (vehicle) 2/6 0/6 No tumors: 49-217d*
GFAP-Cre; Nf1flox/null (pTomo-shNf1;shp53) 3/11 8/11 91d (25-211d)
GFAP-Cre; Nf1flox/flox (vehicle) 0/4 0/4 No tumors:129-153d*
GFAP-Cre; Nf1flox/flox (pTomo-shNf1;shp53) 2/5 3/5 176d (117-298d)
Wild-type (pTomo-shNf1;shp53) 0/4 0/4 No tumors: 182-365d#
Nf1+/− (pTomo-shNf1;shp53) 0/4 0/4 No tumors: 182-365d#
*
Vehicle mice were euthanized and analyzed at time points equivalent to those when p53 shRNA-injected mice were euthanized or at a time when they became ill due to non-tumor-related issues (rectal prolapse or hydrocephalus). The details are provided below:
  • Vehicle-injected GFAP-Cre; Nf1flox/null mice: 2 mice at 49 days, 2 mice at 154 days and 2 mice at 217 days.
  • Vehicle-injected Periostin-Cre; Nf1flox/flox mice: 1 mouse at 83 days, 3 mice at 144 days, 2 mice at 154 days, 2 mice at 230 days, 2 mice at 259 days, and 1 mouse at 304 days.
  • Vehicle-injected GFAP-Cre; Nf1flox/flox mice: 2 mice at 129 days, 1 mouse at 138 days, and 1 mouse at 158 days.
  • Wild-type and Nf1+/− mice: 2 mice at 183 days and 2 mice at 365 days for each group.
#

Wild-type and Nf1+/− mice were euthanized and analyzed at 6 month or 12 month time points, as no mice developed symptoms or non-tumor-related issues.