T. Tanaka et al., CHEMOPREVENTION OF MOUSE URINARY-BLADDER CARCINOGENESIS BY THE NATURALLY-OCCURRING CAROTENOID ASTAXANTHIN, Carcinogenesis, 15(1), 1994, pp. 15-19
The chemopreventive effects of two xanthophylls, astaxanthin (AX) and
canthaxanthin (CX), on urinary bladder carcinogenesis induced by N-but
yl-N(4-hydroxybutyl)nitrosamine (OH-BBN) was investigated in male ICR
mice. Mice were given 250 p.p.m. OH-BBN in drinking water for 20 weeks
and after a 1 week interval with tap water, water containing AX or CX
at a concentration of 50 p.p.m. was administered during subsequent 20
weeks. Other groups of mice were treated with AX or CX alone or untre
ated. At the end of the study (week 41), the incidences of preneoplast
ic lesions and neoplasms in the bladder of mice treated with OH-BBN an
d AX or CX were smaller than those of mice given OH-BBN. In particular
, AX administration after OH-BBN exposure significantly reduced the in
cidence of bladder cancer (transitional cell carcinoma) (P < 0.003). H
owever, the inhibition of the frequencies of such lesions in mice trea
ted with OH-BBN and CX was not significant. Treatment with AX or CX al
so decreased the number/nucleus of silver-stained nucleolar organizer
region proteins (AgNORs), a new index of cell proliferation, in the tr
ansitional epithelium exposed to OH-BBN. Preneoplasms and neoplasms in
duced by OH-BBN, and the antiproliferative potential, was greater for
AX than CX. These results indicate that AX is a possible chemopreventi
ve agent for bladder carcinogenesis and such an effect of AX may be pa
rtly due to suppression of cell proliferation.