Lentinan; i.e., polysaccharides extracted from a kind of black mushroom shi
itake, has been clinically applied as an antitumor and antimetastatic drug,
and has been reported to prevent both chemical and viral carcinogenesis. I
t is known that lentinan affects the tumorous vascular system resulting in
the induction of hemorrhagic necrosis which is dependent on T-cells in the
tumor. Repeated mucosal necrosis-regeneration sequence in chronic ulcerativ
e colitis induced with 3% dextran sulfate sodium led to colorectal carcinog
enesis in azoxymethane-pretreated mice. In the present study, the additive
treatment with lentinan in the azoxymethane-dextran sulfate sodium treated
mice enhanced the colorectal high-grade dysplasia, though not significantly
, and the splenic weight. This may show the proliferation of pathogenic spl
enic T cells resulting in a change for the worse of ulcerative colitis, ane
mia induced with hemorrhage and colorectal carcinogenesis; i.e., high-grade
dysplasia of the mucosa and/or invasive adenocarcinomas of the colorectum.
The present results may recommend chemoimmunotherapy while using lentinan,
but not immunotherapy using lentinan alone, is indicated for the managemen
t of cancer patients.