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. Author manuscript; available in PMC: 2014 May 16.
Published in final edited form as: Gut. 2013 Jun 28;63(1):54–63. doi: 10.1136/gutjnl-2013-305178

Table 1.

Gastrointestinal intraepithelial neoplasia (GIN) incidence in male and female INS-GAS mice at timepoints equivalent to 7 mpi with Helicobacter pylori

Microbial status % Of mice with no dysplasia (score=0)
% Of mice with non-GIN dysplasia* (score 0.5–2.5)
% Of mice with GIN (high-grade dysplasia) (score=3)
% Of mice with invasive neoplasms (score >3)
M (%) F (%) M (%) F (%) M (%) F (%) M (%) F (%)
GF (M=6, F=6) 17 17 83 83 0 0 0 0
rASF (M=10, F=7) 0 14 100 86 0 0 0 0
IF (M=10, F=5) 10 20 90 80 0 0 0 0
mHp (M=6, F=6) 0 66 100 34 0 0 0 0
rASFHp (M=13, F=9) 0 0 31 100 46 0 23 0
IFHp (M=15, F=9) 0 0 7 100 53 0 40 0
*

Non-GIN dysplasia defined as low to moderate grade dysplasia (score 0.5–2.5).

Invasive neoplasms defined as either intramucosal carcinomas (extending into the lamina propria or muscularis mucosae) or carcinomas extending into or beyond the submucosal margins.

similar incidence of high-grade dysplasia in 46% and 53%, and similar incidence of invasive neoplasms in 23% and 40% of rASFHp and IFHp mice, respectively, were significantly higher compared with GF, rASF, IF and mHp-colonised male mice (all p<0.05).

F, female INS-GAS mice; GF, germfree; IF, intestinal flora (undefined SPF); M, male; mHp, monoassociated with H pylori; rASF, restricted ASF.