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. Author manuscript; available in PMC: 2010 Aug 15.
Published in final edited form as: J Cell Biochem. 2009 Aug 15;107(6):1097–1106. doi: 10.1002/jcb.22207

Table 1.

Tumor incidence in Fhit−/− and DKO mice

Genotype Treatment
(weeks)
number of tumors
Tumor
bearing
mice
Total
mice
Tumors/
mouse
≤0.5mm ~1mm ≥2mm Total

Fhit−/− 15 0 0 0 0 0(0) 2 0
NMBA, 15 5 2 0 7 3(75) 4 1,75+1.3

25 0 0 0 0 0(0) 12 0
NMBA, 25 43 21 7 71 22(95.7) 23 3.09±2.37

Fhit−/−Nit1−/−(DKO) 15 1 0 0 1 1(25) 4 0.25±0.5
NMBA, 15 10 3 0 13 6(100) 6 2.25±0.96

25 0 5 1 6 3(18.8) 16 0.313±0.7
NMBA, 25 65 74 28 167 31(96.9) 32 5.03+3.02

Upon dissection, esophagus, stomach, liver, kidney, spleen and intestine were examined and tumors were only found in esophagus and forestomach. Tumors were measured and enumerated by visual inspection. Numbers in parentheses denote percentages of tumor bearing mice. Tumors per mouse was expressed as means and standard deviation and pairs of the mean values were compared by Student t-test for: Fhit−/− vs NMBA-treated Fhit−/− 25 week (P<0.001); DKO untreated vs DKO treated 25 week (P<0.001); untreated groups (P<0.10) and 25 week treated groups (P<0.01).