Eng C P, Sehgal S N, Vézina C
J Antibiot (Tokyo). 1984 Oct;37(10):1231-7. doi: 10.7164/antibiotics.37.1231.
Rapamycin exhibits activity against several ascites and solid transplantable tumors; it is slightly active to inactive against leukemias. On a weight basis, rapamycin was less active than 5-fluorouracil, cyclophosphamide and adriamycin, but rapamycin's maximal activity against Colon 38 tumor was similar to that of 5-fluorouracil and cyclophosphamide. Its activity was such that it significantly inhibited tumor growth at any stage of development. In the active dose range, rapamycin appeared less toxic than the other drugs. In the Colon 38 tumor model, rapamycin at a given dose exhibited the same activity when administered ip, iv, im and sc; upon oral administration, its activity was reduced but not abolished. Rapamycin was compatible with 5-fluorouracil and cyclophosphamide. The sequential treatment 5-fluorouracil-rapamycin-cyclophosphamide was superior to the sequence 5-fluorouracil-adriamycin-cyclophosphamide in protecting Colon 38 tumor-bearing mice. 29-Demethoxyrapamycin exerted only marginal activity against P388 lymphocytic leukemia; it was inactive against B16 melanocarcinoma and Colon 38 solid tumor.
雷帕霉素对几种腹水型和实体可移植肿瘤具有活性;对白血病的活性较弱至无活性。按重量计算,雷帕霉素的活性低于5-氟尿嘧啶、环磷酰胺和阿霉素,但雷帕霉素对结肠38肿瘤的最大活性与5-氟尿嘧啶和环磷酰胺相似。其活性使其在肿瘤发展的任何阶段都能显著抑制肿瘤生长。在有效剂量范围内,雷帕霉素的毒性似乎比其他药物小。在结肠38肿瘤模型中,雷帕霉素在给定剂量下经腹腔注射、静脉注射、肌肉注射和皮下注射时表现出相同的活性;口服给药时,其活性降低但未消除。雷帕霉素与5-氟尿嘧啶和环磷酰胺相容。在保护荷结肠38肿瘤小鼠方面,5-氟尿嘧啶-雷帕霉素-环磷酰胺的序贯治疗优于5-氟尿嘧啶-阿霉素-环磷酰胺的序贯治疗。29-去甲氧基雷帕霉素对P388淋巴细胞白血病仅具有微弱活性;对B16黑色素瘤和结肠38实体瘤无活性。