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小分子免疫调节剂福酚美克与环磷酰胺联合应用对同基因小鼠肿瘤生长及免疫的影响

Effect of forphenicinol, a small molecular immunomodifier, in combination with cyclophosphamide on growth of and immunity to syngeneic murine tumors.

作者信息

Nitta K, Tanaka T, Takeuchi M

出版信息

Cancer Treat Rep. 1985 Mar;69(3):285-91.

PMID:3978657
Abstract

Forphenicinol (FPL) is a low molecular immunomodifier derived from forphenicine, a microbial product found by Umezawa and co-workers. We studied the antitumor effect of FPL, cyclophosphamide (CY), and the combination of the two on several syngeneic murine tumors. The tumors used were mammary carcinoma, L1210 leukemia, B16 melanoma, Lewis lung carcinoma, and glioblastoma. A single ip injection of CY on Day 1 followed by eight consecutive daily oral doses of FPL beginning 6 days after tumor inoculation showed strong cooperation in curing syngeneic mammary carcinoma inoculated intradermally in C3H/HeN mice, most mice being cured of the tumor by the combination therapy and subsequently having acquired strong specific immunity. Treatment with FPL alone (either pre- or post-treatment) also significantly inhibited the growth of the mammary tumor. FPL and CY also showed cooperation in inhibiting the growth of L1210 leukemia transplanted intradermally into CDF1 (BALB/c X DBA/2) mice and markedly prolonged the survival time but FPL treatment alone had no effect. The FPL-CY treatment also affected Lewis lung carcinoma and glioblastoma in syngeneic C57BL/6 mice and produced therapeutic synergism. FPL alone significantly inhibited the growth of B16 melanoma in C57BL/6 mice as well as the syngeneic mammary carcinoma in C3H/HeN mice. These findings suggest that oral administration of FPL in combination with chemotherapeutic agents can be used for treating cancer without causing toxicity, because of the synergistic efficacy of the combination.

摘要

甲砜霉素醇(FPL)是一种低分子免疫调节剂,由梅泽及其同事发现的微生物产物甲砜霉素衍生而来。我们研究了FPL、环磷酰胺(CY)以及二者联合用药对几种同基因小鼠肿瘤的抗肿瘤作用。所使用的肿瘤包括乳腺癌、L1210白血病、B16黑色素瘤、Lewis肺癌和胶质母细胞瘤。在第1天单次腹腔注射CY,然后在肿瘤接种6天后连续8天每日口服FPL,结果显示在治愈C3H/HeN小鼠皮内接种的同基因乳腺癌方面有很强的协同作用,大多数小鼠通过联合治疗治愈了肿瘤,随后获得了强大的特异性免疫力。单独使用FPL治疗(无论是预处理还是后处理)也显著抑制了乳腺肿瘤的生长。FPL和CY在抑制皮内移植到CDF1(BALB/c×DBA/2)小鼠体内的L1210白血病生长方面也显示出协同作用,并显著延长了存活时间,但单独使用FPL治疗没有效果。FPL-CY治疗对同基因C57BL/6小鼠的Lewis肺癌和胶质母细胞瘤也有影响,并产生了治疗协同作用。单独使用FPL显著抑制了C57BL/6小鼠体内B16黑色素瘤以及C3H/HeN小鼠体内同基因乳腺癌的生长。这些发现表明,由于联合用药的协同疗效,口服FPL与化疗药物联合可用于治疗癌症而不产生毒性。

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