STUDY OF INHIBITION OF B16F10 MELANOMA GROWTH IN MICE BY LANDOMYCIN A IN COMPARISON TO DOXORUBICIN

L. V. Lehka, R. R. Panchuk, N. R. Skorokhyd, Yu. S. Kozak, J. Rohr, R. S. Stoika


DOI: http://dx.doi.org/10.30970/sbi.1001.467

Abstract


Landomycin A is a new antibiotic of angucycline group with antineoplastic activity against tumor cells of different origin. In this work, we investigated the effects of landomycin A on the growth of B16F10 mouse melanoma. It was elucidated that studied antibiotic possessed a significant dose-dependent cytotoxic activity against these melanoma cells in vitro, and its LC50 = 2 µM was 5 times lower than that of the doxorubicin, anticancer drug widely used for treatment of solid tumors. Landomycin A at concentration of 10 mg/kg body weight did not cause pathological changes, mortality or general toxic symptoms in intact mice of C57black/6 line. No significant changes in the body weight and hematological parameters of animals treated with landomycin A as compared to the control group were observed. While B16F10 melanoma maintained rapid growth in vivo with a continual increase in tumor volume, landomycin A effectively inhibi­ted tumor growth without a marked myelosuppressive effects or cardio- and hepatotoxicity that are characteristic for doxorubicin action. These results suggest a perspective of landomycin A application in chemotherapy of malignant tumors.


Keywords


landomycin A, melanoma, tumor volume, oxidative therapy

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