Apicidin, a histone deacetylase inhibitor, induces differentiation of HL-60 cells

被引:24
作者
Hong, JJ
Ishihara, K
Yamaki, K
Hiraizumi, K
Ohno, T
Ahn, JW
Zee, O
Ohuchi, K [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Lab Pathophysiol Biochem, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Sungkyunkwan Univ, Coll Pharm, Lab Pharmacognosy, Changan Ku, Suwon 440746, South Korea
[3] RIKEN, Cell Bank, Inst Phys & Chem Res, Tsukuba, Ibaraki 3050074, Japan
[4] Korean Res Inst Chem Technol, Yoosung Ku, Taejon 305343, South Korea
关键词
HL-60; cell; apicidin; trichostatin A; histone deacetylase; differentiation; CD11b;
D O I
10.1016/S0304-3835(02)00500-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The fungal metabolite apicidin (cyclo(N-O-methyl-L-tryptophanyl-L-isoleucinyl-D-pipecolinyl-L-2-amino-8-oxodecanoyl)) inhibited the growth of HL-60 cells in a concentration-dependent manner (100-1000 nM). At higher concentrations (>300 nM), cell death was induced. At 100 nM, it induced hyperacetylation of histone H4 time-dependently, while trichostatin A induced transient hyperacetylation. Apicidin (10-100 nM) increased the cells having nitroblue tetrazolium-reducing activity and expressing CD11b but not CD14 and CD15. The expression of CD11b by apicidin was long lasting, while that by trichostatin A was transient. In K562 cells, apicidin at 10-100 nM did not inhibit cell growth nor express CD11b, CD14 and CD15. Our findings indicate that apicidin inhibits proliferation and induces the early stage of differentiation of HL-60 cells. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:197 / 206
页数:10
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