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阿霉素对小鼠雄激素依赖性紫乃武癌115生长明显无效。

Apparent ineffectiveness of adriamycin for growth of androgen-dependent Shionogi carcinoma 115 in the mouse.

作者信息

Omukai Y, Watanabe S, Nohno T, Senoo T, Saito T

出版信息

Cancer Lett. 1983 Jan;17(3):327-32. doi: 10.1016/0304-3835(83)90171-4.

Abstract

Although adriamycin (1 mg/kg) and 5-fluorouracil (25 mg/kg) were equally effective in inhibiting the growth of Ehrlich carcinoma, both ascites and solid forms, in the mouse, the growth of Shionogi carcinoma 115 in the male DS mouse was relatively resistant to the treatment with adriamycin as compared to 5-fluorouracil. However, direct cytotoxic activity of adriamycin in cultured Shionogi carcinoma 115 (SC 115) cells was about 1000-fold molar potent when compared with 5-fluorouracil. The apparent ineffectiveness of adriamycin against SC 115 in the DS mouse seems to be, at least in part, due to the depression of host defence mechanisms.

摘要

尽管阿霉素(1毫克/千克)和5-氟尿嘧啶(25毫克/千克)在抑制小鼠艾氏腹水癌和实体癌生长方面同样有效,但雄性DS小鼠的癌肉瘤115的生长与5-氟尿嘧啶相比,对阿霉素治疗相对耐药。然而,与5-氟尿嘧啶相比,阿霉素对培养的癌肉瘤115(SC 115)细胞的直接细胞毒性活性在摩尔浓度上要强约1000倍。阿霉素对DS小鼠的SC 115明显无效,这似乎至少部分是由于宿主防御机制的抑制。

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