药效团
细胞毒性
细胞生长
细胞分化
细胞培养
分化疗法
癌变
生物活性
生物
细胞凋亡
维甲酸
药理学
体外
癌症研究
生物化学
细胞生物学
急性早幼粒细胞白血病
遗传学
基因
作者
Eugenia Mata‐Greenwood,Aya Ito,H Westenburg,Bei Cui,Ranjan Mehta,A. Douglas Kinghorn,J.M. Pezzuto
出处
期刊:PubMed
日期:2001-08-11
卷期号:21 (3B): 1763-70
被引量:50
摘要
Non-physiological inducers of terminal differentiation have been used as novel therapies for the prevention and therapy of cancer. We have used cultured HL-60 promyelocytic cells to monitor differentiation, proliferation and cell death events as induced by a large set of extracts derived from plants. Screening of more than 1400 extracts led to the discovery of 34 with potent activity (ED50 <8 mg/ml). Bioassay-guided fractionation led to the isolation of zapotin and 2',5,6-trimethoxyflavone as active principles from Casimiroa edulis, dibenzyltrisulfide and 2-[(phenylmethyl)dithio]ethanol as active principles from Petiveria alliacea, and desmethylrocaglamide from Aglaia ponapensis. Zapotin demonstrated the most favorable biological profile in that induction of differentiation correlated with proliferation arrest, and a lack of cytotoxicity. We conclude that the HL-60 cell model is a useful system for the discovery of novel pharmacophores with potential to suppress the process of carcinogenesis, and that flavonoids may be especially useful in this capacity.
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