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大分子霉素B(NSC 170105)对小鼠白血病、黑色素瘤和肺癌的抗肿瘤活性。

Antitumor activity of macromomycin B (NSC 170105) against murine leukemias, melanoma, and lung carcinoma.

作者信息

Lippman M M, Laster W R, Abbott B J, Venditti J, Baratta M

出版信息

Cancer Res. 1975 Apr;35(4):939-45.

PMID:1116151
Abstract

Mice bearing either of the two rapidly growing mouse leukemias, L1210 or P388, or the slow-growing B16 melanoma responded to i.p. injections of Macromomycin B (NSC 170105) with significant increases in life-span. The maximal increases in life-span obtained in these experiments were 37% for L1210, 68% for P388, and 120% for B16. In addition, there were 7 of 30 cures for varying doses of Macromomycin in the B16 melanoma. Activity of over 50% increase in life-span in B16 was obtained with a daily i.p. injection on Days 1 to 9 of 16 to 40 mg/kg. Animals that had received s.c. implanted Lewis lung tumors responded to either single or repeated injections (8 to 16 mg/kg) given at the site of tumor implant by a marked reduction in growth of the primary tumor, increased life-span, and some cures. The same doses were without effect when administered i.p. The reported activity of Macromomycin against L1210, P388 leukemias, B16 melanoma, and Lewis lung carcinoma make it a good candidate for development for clinical trial against human solid tumors. A new method of evaluating activity against solid tumors, "responder analysis," is also presented.

摘要

携带两种快速生长的小鼠白血病(L1210或P388)或生长缓慢的B16黑色素瘤的小鼠,腹腔注射大分子霉素B(NSC 170105)后,生存期显著延长。在这些实验中,L1210的最大生存期延长率为37%,P388为68%,B16为120%。此外,在B16黑色素瘤中,不同剂量的大分子霉素有30例中有7例治愈。在第1至9天每天腹腔注射16至40mg/kg,可使B16的生存期延长率超过50%。接受皮下植入Lewis肺癌的动物,在肿瘤植入部位单次或重复注射(8至16mg/kg)后,原发肿瘤生长明显减缓,生存期延长,并有部分治愈。相同剂量腹腔注射则无效。大分子霉素对L1210、P388白血病、B16黑色素瘤和Lewis肺癌的报道活性,使其成为开发针对人类实体瘤的临床试验的良好候选药物。还介绍了一种评估对实体瘤活性的新方法,即“反应者分析”。

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