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Chemotherapy and spleen peptides preparation, SP-1, (Polyerga TM) in the treatment of experimental lung metastases of mammary carcinoma in mice (CROSBI ID 77714)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Jurin, Mislav ; Žarković, Neven ; Borović, Suzana ; Hartleb, Martin Chemotherapy and spleen peptides preparation, SP-1, (Polyerga TM) in the treatment of experimental lung metastases of mammary carcinoma in mice // Croatian medical journal, 38 (1997), 4; 317-321

Podaci o odgovornosti

Jurin, Mislav ; Žarković, Neven ; Borović, Suzana ; Hartleb, Martin

engleski

Chemotherapy and spleen peptides preparation, SP-1, (Polyerga TM) in the treatment of experimental lung metastases of mammary carcinoma in mice

Aim. To study the influence of chemotherapy with cyclophosphamide and/or spleen peptides" preparation SP-1, PolyergaTM, on the incidence or experimental lung metastases of mammary carcinoma in mice. Method. Mammary carcinoma cells were injected i.v. into CBA/HZgr mice to obtain experimental lung metastases. One day later, a single injection of cyclophosphamide (50 mg/kg) was given i.p., and/or different concentrations of Polyerga were given perorally in drinking water until the end of the experiment. The mice were killed and the number of lung metastatic nodules determined. Results. Peroral application of PolyergaTM was effective in reducing the number of experimental lung metastases. Even the smallest dose (0.05 mg/kg, 100-fold lower than the dose used in human practice) had statistically significant effect (p=0.042). By increasing the dose of PolyergaTM, its effectiveness was more pronounced. The dose of 5.0 mg/kg was as effective as a 100-fold higher dose, and was chosen for further experiments in combination with cyclophosphamide. Mice treated with the combined therapy were without tumor or the number of metastases was significantly reduced (p<0.00l). Conclusion. PolyergaTM preparation is active against tumor metastases, particularly if combined with the standard chemotherapy.

mammary neoplasms ; experimental ; metastasis ; peptides ; therapy

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Podaci o izdanju

38 (4)

1997.

317-321

objavljeno

0353-9504

1332-8166

Povezanost rada

Temeljne medicinske znanosti

Indeksiranost