Suppr超能文献

FK973对人口腔癌细胞和乳腺癌细胞的细胞毒性活性。

Cytotoxic activity of FK973 against human oral and breast cancer cells.

作者信息

Wu J Z, Adachi I, Watanabe T

机构信息

Central Laboratory, Stomatological Hospital, Fourth Military Medical College, Xi'an.

出版信息

Chin Med J (Engl). 1991 Oct;104(10):834-7.

PMID:1661225
Abstract

FK973 (11-acetyl-8-carbamoyloxymethyl-4-formyl-14-oxa-1, 11-diazatetracyclo [7.4.1.0.0] tetradeca-2, 4, 6-trien-6, 9-diyl diacetate), an analogue of mitomycin C (MMC), was tested against human oral squamous cancer cell lines Ca 9-22, HSC-2, HSC-3, breast adenocarcinoma cell lines MCF-7, BT-20 and breast ductal carcinoma cell line T-47D using MTT assay. FK973 showed cytotoxic effects against six tested cell lines and much wider effective dose range than MMC, adriamycin (ADM), and cisplatin (CDDP). FK973 was the most potent of the four drugs tested against the growth of the three squamous cancer cell lines derived from oral cavity. However, in breast cancer cell lines, FK973 was less potent than MMC and ADM. FK973 was time and dose dependent. The combination effects of FK973 with 5-Fluorouracil (5FU) or CDDP were synthetical. It may be a promising candidate for the treatment of oral and breast cancer.

摘要

FK973(11-乙酰基-8-氨甲酰氧基甲基-4-甲酰基-14-氧杂-1,11-二氮杂四环[7.4.1.0.0]十四碳-2,4,6-三烯-6,9-二基二乙酸酯),一种丝裂霉素C(MMC)的类似物,使用MTT法针对人口腔鳞状癌细胞系Ca 9-22、HSC-2、HSC-3、乳腺癌腺癌细胞系MCF-7、BT-20和乳腺导管癌细胞系T-47D进行了测试。FK973对六种受试细胞系显示出细胞毒性作用,且有效剂量范围比MMC、阿霉素(ADM)和顺铂(CDDP)宽得多。在针对源自口腔的三种鳞状癌细胞系的生长进行测试的四种药物中,FK973是最有效的。然而,在乳腺癌细胞系中,FK973的效力低于MMC和ADM。FK973具有时间和剂量依赖性。FK973与5-氟尿嘧啶(5FU)或CDDP的联合作用是协同的。它可能是治疗口腔癌和乳腺癌的一个有前景的候选药物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验