Cotylenin A-induced differentiation is independent of the transforming growth factor-β signaling system in human myeloid leukemia HL-60 cells

被引:13
作者
Matsunawa, M
Ishii, Y
Kasukabe, T
Tomoyasu, S
Ota, H
Honma, Y
机构
[1] Shimane Univ, Fac Med, Dept Life Sci, Izumo, Shimane 6938501, Japan
[2] Saitama Canc Ctr, Res Inst, Dept Chemotherapy, Komuro Ina, Saitama, Japan
[3] Showa Univ, Sch Med, Dept Hematol, Tokyo 142, Japan
[4] Showa Univ, Sch Med, Dept Pathol 2, Tokyo 142, Japan
关键词
cotylenin A; vitamin D3; transforming growth factor-beta; Smad; differentiation; myeloid leukemia; HL-60;
D O I
10.1080/10428190500375839
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cotylenin A, which has been isolated as a plant growth regulator, potently induces the differentiation of human myeloid leukemia cells. Treatment of HL-60 cells with a combination of transforming growth factor (TGF)-beta and 1 alpha, 25-dihydroxyvitamin D-3 (VD3) resulted in increased differentiation compared to separate treatments, but TGF-beta did not affect the cotylenin A-induced differentiation of HL-60 cells. It is possible that the signal transduction pathway used by cotylenin A for inducing the differentiation of leukemia cells is the same as that used by TGF-beta. However, cotylenin A did not affect the expression of TGF superfamily or Smad genes in HL-60 cells. Treatment with neutralizing anti-TGF-beta antibody or an inhibitor of TGF-beta signaling did not inhibit cotylenin A-induced differentiation, although VD3-induced differentiation was significantly suppressed by these treatments. The subcellular distribution of Smad3 was also unaffected by cotylenin A. These results suggest that the cotylenin A-induced differentiation of leukemia cells is independent of the TGF-beta signaling system, although TGF-beta acts as an autocrine mediator of the growth arrest and differentiation of leukemia cells induced by VD3 and other inducers.
引用
收藏
页码:733 / 740
页数:8
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