Discovery of novel inducers of cellular differentiation using HL-60 promyelocytic cells

被引:0
|
作者
Mata-Greenwood, E
Ito, A
Westenburg, H
Cui, BL
Mehta, RG
Kinghorn, AD
Pezzuto, JM
机构
[1] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Program Collaborat Res Pharmaceut Sci, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Med, Dept Surg Oncol, Chicago, IL 60612 USA
关键词
HL-60; cells; differentiation; natural products; chemoprevention; differentiation therapy; flavones; lignans; polysulfides;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页码:1763 / 1770
页数:8
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