TY - JOUR
T1 - Direct antitumor effect of the polysaccharide levan in mice
T2 - Effects of drug concentration and time and temperature of incubation
AU - Leibovici, Judith
AU - Stark, Yafit
N1 - Funding Information:
I Received September 20,1983; accepted February 7,1984. 2 Partially supported by the Citemick Fund for Medical Research. .1Part of this study was presented at the thirteenth meeting of the Federation of European Biochemical Societies held in Jerusalem in August 1980. This study also represents a part of a thesis submitted by Y. Stark in partial Iulfillment of the requirements for a Ph.D. degree from Tel-Aviv University. 4 Animals were maintained under the guidelines set forth by Tel-Aviv University. 'Department of Pathology, Sackler Faculty of Medicine, Tel-Aviv University, Ramal-Aviv, 69978 Tel-Aviv, Israel. 6We thank Mr. N. Rotschild for the animal care.
PY - 1984/6
Y1 - 1984/6
N2 - In vitro treatment of Lewis lung carcinoma cells with the polysaccharide levan was shown previously to reduce the oncogenicity of these cells by acting on the cell membrane. In the present study the direct effect of levan on the tumorigenicity of Lewis lung carcinoma in C57BL male mice was tested at different doses and intervals and temperatures of incubation. A dose-dependent decrease in tumorigenicity was observed: Doses of 0.5, 1, and 2 mg Ievan/2×105 cells/0.2 ml reduced tumor incidence by 30, 50, and 70%, respectively. Some degree of inhibition was observed even with a dose of 0.004 mg. The inhibitory effect was rapid; 5 minutes of incubation resulted in the same reduction in oncogenicity as 60 minutes. Inhibition at 0°C was as effective as inhibition at 37°C. The lack of temperature effect indicates that enzymatic activity probably is not involved. The data presented here, together with previous data, suggest that levan induces a physical, rather than a chemical, change in the affected tumor cells. The polysaccharide appears to be loosely, noncovalently bound to the cell membrane.
AB - In vitro treatment of Lewis lung carcinoma cells with the polysaccharide levan was shown previously to reduce the oncogenicity of these cells by acting on the cell membrane. In the present study the direct effect of levan on the tumorigenicity of Lewis lung carcinoma in C57BL male mice was tested at different doses and intervals and temperatures of incubation. A dose-dependent decrease in tumorigenicity was observed: Doses of 0.5, 1, and 2 mg Ievan/2×105 cells/0.2 ml reduced tumor incidence by 30, 50, and 70%, respectively. Some degree of inhibition was observed even with a dose of 0.004 mg. The inhibitory effect was rapid; 5 minutes of incubation resulted in the same reduction in oncogenicity as 60 minutes. Inhibition at 0°C was as effective as inhibition at 37°C. The lack of temperature effect indicates that enzymatic activity probably is not involved. The data presented here, together with previous data, suggest that levan induces a physical, rather than a chemical, change in the affected tumor cells. The polysaccharide appears to be loosely, noncovalently bound to the cell membrane.
UR - http://www.scopus.com/inward/record.url?scp=0021252072&partnerID=8YFLogxK
U2 - 10.1093/jnci/72.6.1417
DO - 10.1093/jnci/72.6.1417
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:0021252072
SN - 0027-8874
VL - 72
SP - 1417
EP - 1420
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 6
ER -