LACK OF AN ANTITUMORAL EFFECT OF IMMUNOMODULATORY GALACTOSIDE-SPECIFIC MISTLETOE LECTIN ON N-METHYL-N-NITROSOUREA-INDUCED URINARY-BLADDER CARCINOGENESIS IN RATS
E. Kunze et al., LACK OF AN ANTITUMORAL EFFECT OF IMMUNOMODULATORY GALACTOSIDE-SPECIFIC MISTLETOE LECTIN ON N-METHYL-N-NITROSOUREA-INDUCED URINARY-BLADDER CARCINOGENESIS IN RATS, Experimental and toxicologic pathology, 49(3-4), 1997, pp. 167-180
The aim of the present animal experiment was to study the effect of ga
lactoside-specific lectin or agglutinin (VAA) from mistletoe (Viscum a
lbum L.) on chemically induced tumor development in the urinary bladde
r of rats. Since VAA has been shown to exert a remarkable immunomodula
ting effect, any change in tumor formation would indicate a lectin-tri
ggered immune control of urothelial carcinogenesis in the used model.
To produce vesical neoplasms the direct-acting urothelial carcinogen N
-methyl-N-nitrosourea (MNU) was administered at a single intravesical
dose (7.5 mg/kg body weight). Highly purified VAA was given subcutaneo
usly twice a week at the immunomodulatory dose of 1 ng/kg body weight
over a period of 6 months during the critical phases of tumor developm
ent. After a total experimental time of 15 months the incidence of epi
thelial bladder tumors was 29.3 % in controls versus 27.9 % in rats ad
ditionally receiving the lectin and thus not significantly different i
n both experimental groups. There were, moreover, no substantial diffe
rences in the histopathologic spectrum of epithelial tumors induced, t
heir patterns of growth, grades of cellular malignancy and local exten
sion. The frequency and histopathology of mesenchymal bladder tumors a
s well as the incidence and morphology of carcinomas of the ureters an
d renal pelves also proved to be similar in controls and in rats treat
ed with VAA. In conclusion, the present data provide no evidence for a
modifying or even inhibitory effect of the immunomodulatory galactosi
de-specific mistletoe lectin on experimental urothelial carcinogenesis
.