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[通过KM 2210预处理增强丝裂霉素C对人乳腺癌异种移植瘤的抗肿瘤活性]

[Enhancement of antitumor activity of mitomycin C against human breast carcinoma xenografts by pretreatment with KM 2210].

作者信息

Yamamoto T, Kubota T, Oka S, Josui K, Fujita S, Arisawa Y, Suto A, Inoue S, Kuzuoka M, Ishibiki K

机构信息

Dept. of Surgery, School of Medicine, Keio University.

出版信息

Gan To Kagaku Ryoho. 1990 Jan;17(1):109-14.

PMID:2105084
Abstract

Three human breast carcinoma xenografts, MCF-7, R-27 and T-61 serially transplanted into nude mice were treated with mitomycin C (MMC) alone, KM2210 (estra-1, 3, 5(10)-triene-3, 17 beta-diol, 3 benzoate 17-[4-(4-bis(2-chloroethyl)amino)phenyl)-1-oxobutoxy)acetate) alone and KM2210 followed by MMC. One hundred or 300 mg of KM2210 per kg were administered orally daily from Day 1 to 4 and MMC at the dose of 3 mg/kg was given ip on Day 5. The antitumor activity of MMC on these xenografts was enhanced by pretreatment with KM2210, suggesting a new combination chemo- and endocrine therapy of hormone-dependent human breast carcinomas.

摘要

将三种人乳腺癌异种移植瘤(MCF - 7、R - 27和T - 61,它们被连续移植到裸鼠体内)分别单独用丝裂霉素C(MMC)、单独用KM2210(雌甾 - 1,3,5(10) - 三烯 - 3,17β - 二醇,3 - 苯甲酸酯17 - [4 - (4 - 双(2 - 氯乙基)氨基)苯基] - 1 - 氧代丁氧基)乙酸酯)以及先用KM2210再用MMC进行处理。从第1天到第4天,每天按每千克100或300毫克的剂量口服KM2210,在第5天腹腔注射剂量为3毫克/千克的MMC。KM2210预处理增强了MMC对这些异种移植瘤的抗肿瘤活性,提示了一种针对激素依赖性人乳腺癌的新的化疗与内分泌联合治疗方法。

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