Fungal malformins inhibit bleomycin-induced G2 checkpoint in Jurkat cells

被引:30
作者
Hagimori, Keiichi
Fukuda, Takashi
Hasegawa, Yoko
Omura, Satoshi
Tomoda, Hiroshi
机构
[1] Kitasato Univ, Sch Pharm, Minato Ku, Tokyo 1088641, Japan
[2] Kitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
[3] Kitasato Univ, Grad sch Infect Control Sci, Tokyo, Japan
[4] Kitasato Inst, Minato Ku, Tokyo 1088642, Japan
关键词
malformin C; G2 checkpoint inhibitor; cell cycle. anti-cancer agent; bleomycin; fungal metabolite;
D O I
10.1248/bpb.30.1379
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A DNA-damaging agent, bleomycin, arrests the cell cycle at the G2 phase of Jurkat cells, which are defective in the G1 checkpoint, while microtubule-disrupting colchicine arrests it at M phase. Fungal cyclopeptides, malformin A 1 and malformin C, were found to abrogate bleomycin-induced G2 arrest (IC50; 0.48 mu M and 0.9 nM, respectively), resulting in a drastic decrease in cells in G2 phase and increase in cells in subG1 phase. On the other hand, malformins showed little effect on the colchicine-induced M phase arrest in Jurkat cells (IC50; 2.7 mu M and 24 nM, respectively). Malformin C (0.026 mu M) also abrogated bleomycin-induced G2 arrest in colon cancer-derived HCT-116 cells. These data strongly suggest that malformin C disrupted the cell cycle at the G2 checkpoint of cancer cells, leading to sensitization of the cancer cells to the anti-cancer reagent.
引用
收藏
页码:1379 / 1383
页数:5
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