Geranylgeranyl diphosphate depletion inhibits breast cancer cell migration

被引:23
作者
Dudakovic, Amel [1 ]
Tong, Huaxiang [2 ]
Hohl, Raymond J. [1 ,2 ]
机构
[1] Univ Iowa, Dept Pharmacol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
关键词
Isoprenoid; Mevalonate; Digeranyl bisphosphonate; Geranylgeranyl diphosphate; Geranylgeranyl diphosphate synthase; Migration; ACUTE MYELOID-LEUKEMIA; ISOPRENOID BISPHOSPHONATES; PROTEIN GERANYLGERANYLATION; I INHIBITOR; RHO-GTPASES; PYROPHOSPHATE SYNTHASE; FARNESYLTRANSFERASE; FARNESYL; THERAPY; RAS;
D O I
10.1007/s10637-010-9446-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objective of this study was to determine whether geranylgeranyl diphosphate synthase inhibition, and therefore geranylgeranyl diphosphate depletion, interferes with breast cancer cell migration. Digeranyl bisphosphonate is a specific geranylgeranyl diphosphate synthase inhibitor. We demonstrate that digeranyl bisphosphonate depleted geranylgeranyl diphosphate and inhibited protein geranylgeranylation in MDA-MB-231 cells. Similar to GGTI-286, a GGTase I inhibitor, digeranyl bisphosphate significantly inhibited migration of MDA-MB-231 cells as measured by transwell assay. Similarly, digeranyl bisphosphonate reduced motility of MDA-MB-231 cells in a time-dependent manner as measured by large scale digital cell analysis system microscopy. Digeranyl bisphosphonate was mildly toxic and did not induce apoptosis. Treatment of MDA-MB-231 cells with digeranyl bisphosphonate decreased membrane while it increased cytosolic RhoA localization. In addition, digeranyl bisphosphonate increased RhoA GTP binding in MDA-MB-231 cells. The specificity of geranylgeranyl diphosphonate synthase inhibition by digeranyl bisphosphonate was confirmed by exogenous addition of geranylgeranyl diphosphate. Geranylgeranyl diphosphate addition prevented the effects of digeranyl bisphosphonate on migration, RhoA localization, and GTP binding to RhoA in MDA-MB-231 cells. These studies suggest that geranylgeranyl diphosphate synthase inhibitors are a novel approach to interfere with cancer cell migration.
引用
收藏
页码:912 / 920
页数:9
相关论文
共 46 条
[1]   Zoledronic acid induces apoptosis and inhibits adhesion to mineralized matrix in prostate cancer cells via inhibition of protein prenylation [J].
Coxon, JP ;
Oades, GM ;
Kirby, RS ;
Colston, KW .
BJU INTERNATIONAL, 2004, 94 (01) :164-170
[2]   The large-scale digital cell analysis system: An open system for nonperturbing live cell imaging [J].
Davis, Paul J. ;
Kosmacek, Elizabeth A. ;
Sun, Yuansheng ;
Ianzini, Fiorenza ;
Mackey, Michael A. .
JOURNAL OF MICROSCOPY, 2007, 228 (03) :296-308
[3]   Targeting ras signalling pathways in cancer therapy [J].
Downward, J .
NATURE REVIEWS CANCER, 2003, 3 (01) :11-22
[4]   Inhibition of geranylgeranyl diphosphate synthase induces apoptosis through multiple mechanisms and displays synergy with inhibition of other isoprenoid biosynthetic enzymes [J].
Dudakovic, Amel ;
Wiemer, Andrew J. ;
Lamb, Kimberly M. ;
Vonnahme, Laura A. ;
Dietz, Sara E. ;
Hohl, Raymond J. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 324 (03) :1028-1036
[5]  
Fritz G, 1999, INT J CANCER, V81, P682, DOI 10.1002/(SICI)1097-0215(19990531)81:5<682::AID-IJC2>3.0.CO
[6]  
2-B
[7]   ROLE OF PROTEIN MODIFICATION REACTIONS IN PROGRAMMING INTERACTIONS BETWEEN RAS-RELATED GTPASES AND CELL-MEMBRANES [J].
GLOMSET, JA ;
FARNSWORTH, CC .
ANNUAL REVIEW OF CELL BIOLOGY, 1994, 10 :181-205
[8]  
GRUNDY SM, 1988, NEW ENGL J MED, V319, P24
[9]  
Gunning WT, 2003, CLIN CANCER RES, V9, P1927
[10]   A phase 2 study of the oral farnesyltransferase inhibitor tipifarnib in patients with refractory or relapsed acute myeloid leukemia [J].
Harousseau, Jean-Luc ;
Lancet, Jeffrey E. ;
Reiffers, Josy ;
Lowenberg, Bob ;
Thomas, Xavier ;
Huguet, Francoise ;
Fenaux, Pierre ;
Zhang, Steven ;
Rackoff, Wayne ;
De Porre, Peter ;
Stone, Richard .
BLOOD, 2007, 109 (12) :5151-5156