Z-Phe-Gly-NHO-Bz, an inhibitor of cysteine cathepsins, induces apoptosis in human cancer cells

被引:0
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作者
Zhu, DM
Uckun, FM
机构
[1] Parker Hughes Inst, Ctr Canc, Dept Immunol, St Paul, MN 55113 USA
[2] Parker Hughes Inst, Ctr Canc, Dept Expt Oncol, St Paul, MN 55113 USA
[3] Parker Hughes Inst, Ctr Canc, Drug Discovery Program, St Paul, MN 55113 USA
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
An increasing number of studies indicate that cysteine cathepsins contribute to cancer progression, invasion, and metastasis. Here we provide experimental evidence that the cathepsin inhibitor Z-Phe-Gly-NHO-Bz induces rapid apoptotic death in human cancer cell lines. Notably, the Z-Phe-Gly-NHO-Bz-induced apoptosis exhibited independence of p53, caspases. and mitogen-activated protein (MAP) kinases. Taken together, our results prompt the hypothesis that cysteine cathepsin(s) is a universal survival factor for cancer cells, and its inhibition leads to cancer cell apoptosis. The exquisite sensitivity of human cancer cells to CATI-1 indicates that this compound and its derivatives may provide the basis for new treatment programs against abroad spectrum of malignancies.
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页码:2064 / 2069
页数:6
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