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. Author manuscript; available in PMC: 2012 Jun 1.
Published in final edited form as: Cancer Prev Res (Phila). 2011 Mar 7;4(6):890–896. doi: 10.1158/1940-6207.CAPR-10-0369

Table 2. Histopathology of Wild Type and Transgenic Mice Receiving Different Doses of DIM for 20 Weeks.

Histopathological Response dichotomized as CIN free or not. For thebinary outcome, CIN freedom, Cochran-Armitage Test for trend, reported significant DIM Dose effect in Transgenic mice (P<0.0001) and not significant in Wild type (P=0.5327). Cochran –Armitage exact test with Hochberg procedure for multiple testing, identified 1000ppm as the minimum effective dose (MED) at (P<0.05)

Cervical Epithelium 0ppm DIM 500ppm DIM 1000ppm DIM 1500ppm DIM 2000ppm DIM 2500ppm DIM
Transgenic
CIN-free 3 4 13 14 13 14
CIN1 1 3 2 0 0 1
CIN2 5 9 4 5 9 5
CIN3 6 5 2 3 1 1
Carcinoma in situ (NCIS) 2 0 0 0 0 0
Squamous Cell carcinoma (SCC) 2 1 0 0 0 0
Total mice (Transgenic) 19 22 21 22 23 21
Percent CIN-free/Total 16% 18% 62% 64% 57% 67%
Wildtype
CIN-free 26 27 21 18 19 20
CIN1 5 5 0 5 2 4
CIN2 3 0 0 2 4 2
Wildtype Total 34 32 21 25 25 26
Percent CIN-free/Total 76% 84% 100% 72% 76% 77%