I. Vucenik et al., INHIBITION OF RAT MAMMARY CARCINOGENESIS BY INOSITOL HEXAPHOSPHATE (PHYTIC ACID) - A PILOT-STUDY, Cancer letters, 75(2), 1993, pp. 95-102
Since phytic acid (inositol hexaphosphate, InsP6) and inositol (Ins) h
ave been demonstrated to have anti-tumor and anti-cell proliferative a
ction in several experimental models of carcinogensis, in a pilot stud
y we have examined their effect on 7,12-dimethylbenz(a)anthracene (DMB
A)-induced rat mammary tumor model. Starting a week prior to induction
with DMBA. the drinking water of female Sprague-Dawley rats was suppl
emented with either: 15 mM InsP6, 15 mM Ins, or 15 mM InsP6 + 15 mM In
s; a control group received no inositol compounds. Animals (55-day-old
) were given a single dose of DMBA (20 mg) in 1 ml of sesame oil by or
al intubation. Four additional groups not receiving DMBA, but drinking
tap water, InsP6, Ins, or InsP6 + Ins of the same molarity as experim
ental groups were observed for the duration of the study to monitor fo
r any putative toxicity following this long-term treatment. As opposed
to the DMBA-only group, rats treated with InSP6 +/- Ins showed a 48%
reduction in the number of tumors/tumor bearing animal (tumor multipli
city) and a 40% reduction in the number of tumors/rat. In contrast to
20% rats in DMBA-only group, only 0-8% animals in the treatment group
had 5 or more tumors. Likewise, the tumor incidence was reduced by 19%
in InsP6 +/- Ins as compared to control untreated animals. The tumors
in the treated groups were also 16% smaller in size. Data from this p
ilot study suggest that in addition to being effective against colon c
ancer, InsP6 +/- Ins may be protective against mammary carcinoma as we
ll; additional studies are however warranted.