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抗转移、抗侵袭和细胞毒性药物对小鼠可移植性白血病生长和扩散的影响。

Effects of antimetastatic, antiinvasive and cytotoxic agents on the growth and spread of transplantable leukemias in mice.

作者信息

Sava G, Giraldi T, Perissin L, Zorzet S, Decorti G

出版信息

Clin Exp Metastasis. 1987 Jan-Mar;5(1):27-34. doi: 10.1007/BF00116623.

Abstract

The effects of cytotoxic (cyclophosphamide, CCNU, GANU), antiinvasive (vincristine, vinblastine) and antimetastatic (ICRF-159, DM-COOK) agents have been compared in mice-bearing P388 and L1210 leukemias, and TLX5 lymphoma. The drugs tested increase the survival time of the treated mice in a manner consistent with a cytotoxic action in the case of cyclophosphamide, CCNU, GANU, vincristine and vinblastine. Leukemic infiltration of the brain after i.p. tumor implantation has been determined by bioassay of this organ, and is reduced by treatment with all of the drugs tested, with the exception of ICRF-159. DM-COOK appears to increase the life-span of the treated animals by the inhibition of leukemic spread rather than by a cytotoxic action. The marked cytotoxicity of vincristine and vinblastine is sufficient to account for failure to detect any antimetastatic effects of these agents. The lack of antidisseminative effect observed for ICRF-159 under the experimental conditions employed might be connected with the observation that the antimetastatic action of this drug on solid tumors is due to its effects on tumor blood vessels.

摘要

在携带P388和L1210白血病以及TLX5淋巴瘤的小鼠中,对细胞毒性药物(环磷酰胺、洛莫司汀、甘磷酰芥)、抗侵袭药物(长春新碱、长春碱)和抗转移药物(ICRF - 159、DM - COOK)的效果进行了比较。所测试的药物以与环磷酰胺、洛莫司汀、甘磷酰芥、长春新碱和长春碱的细胞毒性作用相一致的方式增加了治疗小鼠的存活时间。腹腔注射肿瘤细胞后,通过对脑器官的生物测定确定脑内白血病浸润情况,除ICRF - 159外,所有测试药物的治疗均可使其减少。DM - COOK似乎是通过抑制白血病扩散而非细胞毒性作用来延长治疗动物的寿命。长春新碱和长春碱显著的细胞毒性足以解释未能检测到这些药物的任何抗转移作用。在所采用的实验条件下,未观察到ICRF - 159的抗扩散作用,这可能与该药物对实体瘤的抗转移作用是由于其对肿瘤血管的影响这一观察结果有关。

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