The bisphosphonate pamidronate is a potent inhibitor of human osteosarcoma cell growth in vitro

被引:74
作者
Sonnemann, J [1 ]
Eckervogt, V [1 ]
Truckenbrod, B [1 ]
Boos, J [1 ]
Winkelmann, W [1 ]
van Valen, F [1 ]
机构
[1] Univ Klinikum Munster, Klin & Poliklin Allgemeine Orthopadie, Lab Expt Orthopadie Zellbiol, D-48149 Munster, Germany
关键词
bisphosphonates; bone tumor; clodronate; mevastatin; osteosarcoma; pamidronate;
D O I
10.1097/00001813-200106000-00007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bisphosphonates (BPs), such as pamidronate and clodronate, are an important class of drugs for the treatment of bone diseases. It is widely recognized that they inhibit bone resorption by suppressing the action of osteoclasts through antagonizing the mevalonate pathway, thereby reducing osteolytic bone metastases derived from different cancers, i.e. breast carcinoma and multiple myeloma, In contrast, the effects of BPs on primary bone tumors is an issue still to be resolved. Therefore, a systematic approach was set up to test the hypothesis that BPs could act directly on osteosarcoma cells. The effects of pamidronate and clodronate on seven osteosarcoma cell lines (HOS, MG-63, OST, SaOS-5, SJSA-1, U2OS and ZK-58) were studied. Pamidronate inhibited cell growth in a time- and dose-dependent manner, and decreased proliferation for up to 73% at 50 muM after 72 h, whereas its monophosphonate analog 3-aminopropyl phosphonate did not reduce cell viability at concentrations up to 2 mM, Clodronate showed less inhibitory effects (maximally 38% reduction at 1 mM after 72 h), Importantly, cell growth of fibroblasts was only very weakly affected by treatment with pamidronate. These results suggest that pamidronate may be a useful agent for the treatment of patients with osteosarcoma. [(C) 2001 Lippincott Williams & Wilkins,].
引用
收藏
页码:459 / 465
页数:7
相关论文
共 25 条
[1]   Pharmacokinetics of pamidronate disodium in patients with cancer with normal or impaired renal function [J].
Berenson, JR ;
Rosen, L ;
Vescio, R ;
Lau, HS ;
Woo, M ;
Sioufi, A ;
Kowalski, O ;
Knight, RD ;
Seaman, JJ .
JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 37 (04) :285-290
[2]   Current use of bisphosphonates in oncology [J].
Body, JJ ;
Bartl, R ;
Burckhardt, P ;
Delmas, PD ;
Diel, IJ ;
Fleisch, H ;
Kanis, JA ;
Kyle, RA ;
Mundy, GR ;
Paterson, AHG ;
Rubens, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3890-3899
[3]   Antitumour effects of bisphosphonates - First evidence and possible mechanisms [J].
Diel, IJ .
DRUGS, 2000, 59 (03) :391-399
[4]   COMPETITIVE INHIBITION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE BY ML-236A AND ML-236B FUNGAL METABOLITES, HAVING HYPOCHOLESTEROLEMIC ACTIVITY [J].
ENDO, A ;
KURODA, M ;
TANZAWA, K .
FEBS LETTERS, 1976, 72 (02) :323-326
[5]   THE SUBCELLULAR-DISTRIBUTION OF [C-14]DICHLOROMETHYLENEBISPHOSPHONATE AND [C-14]1-HYDROXYETHYLIDENE-1,1-BISPHOSPHONATE IN CULTURED CALVARIA CELLS [J].
FELIX, R ;
GUENTHER, HL ;
FLEISCH, H .
CALCIFIED TISSUE INTERNATIONAL, 1984, 36 (01) :108-113
[6]   Alendronate mechanism of action:: geranylgeraniol, an intermediate in the mevalonate pathway, prevents inhibition of osteoclast formation, bone resorption, and kinase activation in vitro [J].
Fisher, JE ;
Rogers, MJ ;
Halasy, JM ;
Luckman, SP ;
Hughes, DE ;
Masarachia, PJ ;
Wesolowski, G ;
Russell, RGG ;
Rodan, GA ;
Reszka, AA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (01) :133-138
[7]   Bisphosphonates: Mechanisms of action [J].
Fleisch, H .
ENDOCRINE REVIEWS, 1998, 19 (01) :80-100
[8]   Clodronate and liposome-encapsulated clodronate are metabolized to a toxic ATP analog, adenosine 5'-(beta,gamma-dichloromethylene) triphosphate, by mammalian cells in vitro [J].
Frith, JC ;
Monkkonen, J ;
Blackburn, GM ;
Russell, RGG ;
Rogers, MJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (09) :1358-1367
[9]   Bisphosphonates induce breast cancer cell death in vitro [J].
Fromigue, O ;
Lagneaux, L ;
Body, JJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (11) :2211-2221
[10]   Effect of alendronate on cultured normal human osteoblasts [J].
García-Moreno, C ;
Serrano, S ;
Nacher, M ;
Farré, M ;
Díez, A ;
Mariñoso, ML ;
Carbonell, J ;
Mellibovsky, L ;
Nogués, X ;
Ballester, J ;
Aubía, J .
BONE, 1998, 22 (03) :233-239