T. Takahashi et al., Inhibitory effect of microfibril wheat bran on azoxymethane-induced colon carcinogenesis in CF1 mice, CANCER LETT, 141(1-2), 1999, pp. 139-146
Microfibril wheat bran (MFW), a processed dietary fiber prepared by milling
of coarse wheat bran (WB), is softer and has a more pleasant taste than WE
. In this study, we examined the inhibitory effect of MFW on azoxymethane (
AOM)-induced colon carcinogenesis in female CF1 mice and compared its effec
t with that of WE and cellulose (CL). The mice were fed a modified AIN 76 A
diet supplemented with either MFW, WE, or CL at a final concentration of 2
0% (w/w). Six weekly s.c. injections of AOM (10 mg/kg body weight) were adm
inistered per mouse commencing I week after the start of the feeding period
. Control mice were injected with saline only. Thirty-three weeks after the
initial injection, the mice were sacrificed, examined for tumors, and the
cecal contents were analyzed to determine the moisture content and the conc
entrations of short-chain fatty acids (SCFA). The average number of total t
umors per mouse in the MFW (2.9 +/- 0.6, P = 0.017) and WE (5.3 +/- 1.3, P
= 0.373) diet groups was lower than that of the CL diet group (7.5 +/- 1.3)
, though there was no significant difference in tumor incidence (94.7%, 90.
0% and 94.7%, respectively) between the groups. More than 90% of the tumors
in each group were adenocarcinomas. The incidence of adenoma and that of c
arcinoma in situ in the MFW diet group (5.3% and 0%, respectively) were als
o lower than those in the CL diet group (26.3 and 26.3%, respectively; P =
0.180 and P = 0.046, respectively). Analysis of the cecal contents revealed
a significantly higher moisture content and significantly higher concentra
tions of SCFA, butyrate in particular, in the MFW and WE diet groups. The r
esults of this study indicate that the source and texture of dietary fiber
can influence tumor development in CF1 mice, and more specifically that MFW
is a promising and useful dietary supplement with properties serving to pr
otect against the development of colon cancer. (C) 1999 Elsevier Science Ir
eland Ltd. All rights reserved.