Anti-tumour activity of zoledronic acid

被引:52
作者
Clézardin, P [1 ]
机构
[1] RTH Laennec, INSERM, U664, Fac Med, F-69372 Lyon 08, France
关键词
zoledronic acid; bisphosphonates; anti-tumour; cancer; angiogenesis; metastases; apoptosis;
D O I
10.1016/j.ctrv.2005.09.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bisphosphonates are proven to be effective in the treatment of benign or malignant skeletal diseases characterized by enhanced osteoclastic bone resorption. Nitrogen-containing bisphosphonates (N-BPs) have also been demonstrated to exhibit direct anti-tumour effects. They not only inhibit proliferation and induce apoptosis in cultured cancer cells, but additionally interfere with adhesion of cancer cells to the bone matrix and inhibit cell migration and invasion. These effects are potentiated when N-BPs are combined with anticancer drugs like taxoids, doxorubicin or imatinib. Zotedronic acid is a highly potent N-BP that has been particularly well investigated, preclinically and in clinical practice. Growing preclinical evidence shows that zoledronic acid also exhibits direct anti-tumour activity. The overall effects on tumour cells appear to be mediated via diverse pathways, such as apoptosis, angiostasis, cell-cell-interactions and immunomodulation. The current insights and fronts of ongoing research are reviewed. Higher doses of zoledronic acid or more frequent applications than currently approved may be required to achieve clinically meaningful anti-tumour effects. The future challenge is to focus on optimizing dosing regimens and drug combinations to maximize the anti-tumour potential of zoledronic acid and to take advantage of the observed synergy with standard neoplastic agents. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:S1 / S8
页数:8
相关论文
共 43 条
[1]   The bisphosphonate zoledronic acid inhibits the development of plasmacytoma induced in BALB/c mice by intraperitoneal injection of pristane [J].
Avcu, F ;
Ural, AU ;
Yilmaz, MI ;
Ozcan, A ;
Ide, T ;
Kurt, B ;
Yalcin, A .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2005, 74 (06) :496-500
[2]   Visualization of bisphosphonate-induced caspase-3 activity in apoptotic osteoclasts in vitro [J].
Benford, HL ;
McGowan, NWA ;
Helfrich, MH ;
Nuttall, ME ;
Rogers, MJ .
BONE, 2001, 28 (05) :465-473
[3]   Zoledronate sensitizes endothelial cells to tumor necrosis factor-induced programmed cell death -: Evidence for the suppression of sustained activation of focal adhesion kinase and protein kinase B/Akt [J].
Bezzi, M ;
Hasmim, M ;
Bieler, G ;
Dormond, O ;
Rüegg, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (44) :43603-43614
[4]  
Boissier S, 1997, CANCER RES, V57, P3890
[5]   The role of bisphosphonates in breast and prostate cancers [J].
Brown, JE ;
Neville-Webbe, H ;
Coleman, RE .
ENDOCRINE-RELATED CANCER, 2004, 11 (02) :207-224
[6]   The farnesyl transferase inhibitor R115777 (Zarnestra®) synergistically enhances growth inhibition and apoptosis induced on epidermoid cancer cells by Zoledronic acid (Zometa®) and Pamidronate [J].
Caraglia, M ;
D'Alessandro, AM ;
Marra, M ;
Giuberti, G ;
Vitale, G ;
Viscomi, C ;
Colao, A ;
Del Prete, S ;
Tagliaferri, P ;
Tassone, P ;
Budillon, A ;
Venuta, S ;
Abbruzzese, A .
ONCOGENE, 2004, 23 (41) :6900-6913
[7]   Bisphosphonates and cancer-induced bone disease:: Beyond their antiresorptive activity [J].
Clézardin, P ;
Ebetino, FH ;
Fournier, PGJ .
CANCER RESEARCH, 2005, 65 (12) :4971-4974
[8]   Estimation of metabolic flux from dominant rate constants in vivo: application to brain and heart [J].
Cohen, DM ;
Bergman, RN .
METABOLIC ENGINEERING, 2004, 6 (01) :59-74
[9]   Bisphosphonates: Clinical experience [J].
Coleman, RE .
ONCOLOGIST, 2004, 9 :14-27
[10]  
Corey E, 2003, CLIN CANCER RES, V9, P295