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Bull Exp Biol Med ; 132(2): 787-90, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11713568

ABSTRACT

We studied the effect of macrophage stimulator water-soluble beta-(1-->3)-D-carboxymethylglucan on the efficiency of cyclophosphamide chemotherapy in Lewis lung carcinoma. Cyclophosphamide inhibited the growth of primary tumor nodes by 57%. The preparation possessed pronounced antimetastatic activity: metastases were found in 40.9% animals. Combination therapy with cyclophosphamide and (1-->3)-beta;-D-glucan inhibited the growth of intramuscular tumors by 75-89% and reduced the incidence of metastases into the lungs by 92-94%. The therapeutic effect was most pronounced after simultaneous administration of these preparations: tumor growth was suppressed by 89.3% and metastases were found in only 7.5% animals (vs. 100% in the control). The potentiating effect of beta-(1-->3)-D-carboxymethylglucan is related to accumulation of cysteine proteinase inhibitors in the tumor tissue and plasma, but not to changes in blood cell composition.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Lewis Lung/drug therapy , Glucans/administration & dosage , beta-Glucans , Animals , Antineoplastic Agents, Alkylating/administration & dosage , Antineoplastic Agents, Alkylating/therapeutic use , Body Weight/drug effects , Carcinoma, Lewis Lung/metabolism , Carcinoma, Lewis Lung/pathology , Cathepsin B/analysis , Cathepsin L , Cathepsins/analysis , Cyclophosphamide/administration & dosage , Cyclophosphamide/therapeutic use , Cystatin A , Cystatin C , Cystatins/blood , Cysteine Endopeptidases , Drug Synergism , Injections, Intraperitoneal , Lung Neoplasms/secondary , Macrophages/drug effects , Male , Mice , Mice, Inbred C57BL , Mice, Inbred CBA , Neoplasm Transplantation
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