Anti-Angiogenic Property of Zoledronic Acid by Inhibition of Endothelial Progenitor Cell Differentiation

被引:69
作者
Yamada, Jun [1 ]
Tsuno, Nelson H. [2 ]
Kitayama, Joji
Tsuchiya, Takeshi
Yoneyama, Satomi
Asakage, Masahiro
Okaji, Yurai [2 ]
Shuno, Yasutaka
Nishikawa, Takeshi
Tanaka, Junichiro
Takahashi, Koki [2 ]
Nagawa, Hirokazu
机构
[1] Univ Tokyo, Dept Surg Oncol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Fac Med, Dept Transfus Med, Tokyo 1130033, Japan
关键词
zoledronic acid; bisphosphonate; angiogenesis; endothelial progenitor cell; BREAST-CANCER CELLS; PROSTATE-CANCER; MEMBRANE LOCALIZATION; MEVALONATE PATHWAY; BISPHOSPHONATE; GROWTH; APOPTOSIS; NEOVASCULARIZATION; HYPERCALCEMIA; COMPLICATIONS;
D O I
10.1016/j.jss.2008.01.031
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
Background. Zoledronic acid (ZOL) is clinically available for the treatment of skeletal complications. In preclinical studies, strong anti-cancer activities against breast cancer, prostate cancer, and leukemia were reported. It also inhibited the proliferation of cultured human endothelial cells, suggestive of an anti-angiogenic activity. Since ZOL has the tendency to accumulate in bone, we investigated the effect of ZOL on endothelial progenitor cells (EPCs), which originate from the bone marrow, and play important roles in angiogenesis. Materials and methods. Human peripheral blood mononuclear cells were cultured for 7 d to differentiate into EPCs. Cells were treated without/with ZOL or with geranylgeraniol (GGOH). Their endothelial phenotype was confirmed by the expression of CD144 and vascular endothelial growth factor receptor 2 and the tube-like formation ability on Matrigel (Becton Dickinson, Bedford, MA). Annexin V/propidium iodide staining was used to analyze apoptosis. Results. ZOL treatment, even at low doses, from d 2 to 7 of culture resulted in impaired EPC differentiation and could be restored by co-treatment with GGOH. On the other hand, treatment of putative EPCs with ZOL at concentrations higher than 10 gm resulted in induction of apoptosis. Conclusion. ZOL dose-dependently inhibited the differentiation of EPCs, the effect being observed even at low drug levels. At high concentrations, ZOL also induced the apoptotic death of putative EPCs. Since GGOH restored the inhibitory effect of ZOL on EPCs differentiation, the effect of ZOL appears to be dependent on the inhibition of prenylation of small-G-proteins. From these findings, we conclude that ZOL could be a potential anticancer agent by inhibiting angiogenesis. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:115 / 120
页数:6
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