Effects of lentinan on colorectal carcinogenesis in mice with ulcerative colitis

Citation
T. Mitamura et al., Effects of lentinan on colorectal carcinogenesis in mice with ulcerative colitis, ONCOL REP, 7(3), 2000, pp. 599-601
Citations number
12
Categorie Soggetti
Oncology
Journal title
ONCOLOGY REPORTS
ISSN journal
1021335X → ACNP
Volume
7
Issue
3
Year of publication
2000
Pages
599 - 601
Database
ISI
SICI code
1021-335X(200005/06)7:3<599:EOLOCC>2.0.ZU;2-Y
Abstract
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.