The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
ANTITUMOR ACTIVITIES OF (2"R)-4'-NHO-TETRAHYDROPYRANYLADRIAMYCIN (THP) AND ITS COMBINATION WITH OTHER ANTITUMOR AGENTS ON MURINE TUMORS
YOSHIYUKI MATSUSHITAHIROYUKI KUMAGAIAKIHIRO YOSHIMOTOHIROSHI TONETOMOYUKI ISHIKURATOMIO TAKEUCHIHAMAO UMEZAWA
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1985 Volume 38 Issue 10 Pages 1408-1419

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Abstract

(2"R)-4'-O-Tetrahydropyranyladriamycin (THP) is a new derivative of doxorubicin (adriamycin, ADM). The concentrations of THP and ADM required to inhibit by 50% the growth of a cultured L1210 cells was 0.003μg/ml and 0.016μg/ml, respectively. Various therapeutic designs of combinations of THP with other antitumor agents were investigated in viva using the L1210 murine leukemia. The combination of THP with cytosine arabinoside (Ara-C), cyclocytidine hydrochloride (Cyclo-C), 6-mercaptopurine (6-MP) and cyclophosphamide (EX) showed a great effectiveness following daily intraperitoneal treatment from days I to 10. High therapeutic effects were also obtained with the combinations of THP with Ara-C, Cyclo-C, vincristine (VCR) and EX following intravenous combination therapy one day following implantation of L1210 leukemia. Schedule dependency and its therapeutic efficacy of THP were examined. THP showed almost the same antitumor activity on the solid-type sarcoma-180 or solid-type Ehrlich carcinoma as ADM by intraperitoneal or intravenous treatment. THP showed some superior activity to ADM in the advanced stage of L1210 leukemia. High antitumor activity of THP on murine leukemia L1210 has been reported by TSURUO et al. (Cancer Res. 42 : 1462-1467, 1982) and was also confirmed. THP gave many mice cures, especially in the intravenous treatment.

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© Japan Antibiotics Research Association
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