In vitro studies in a myelogenous leukemia cell line suggest an organized binding of geranylgeranyl diphosphate synthase inhibitors

被引:2
作者
Reilly, Jacqueline E. [1 ]
Zhou, Xiang [2 ]
Tong, Huaxiang [3 ]
Kuder, Craig H. [3 ]
Wiemer, David F. [2 ]
Hohl, Raymond J. [1 ,3 ,4 ,5 ]
机构
[1] Univ Iowa, Dept Pharmacol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[4] Penn State Univ, Penn State Hershey Canc Inst, Dept Med, Hershey, PA 17033 USA
[5] Penn State Univ, Penn State Hershey Canc Inst, Dept Pharmacol, Hershey, PA 17033 USA
关键词
Isoprenoid; Protein isoprenylation; Geranylgeranyl diphosphate synthase; Bisphosphonate; Statin; Chronic myelogenous leukemia (CML); HMG-COA REDUCTASE; ISOPRENOID BISPHOSPHONATES; BIOLOGICAL-ACTIVITY; CANCER; PROTEIN; STATINS; ACID; VIVO; DEGRADATION; METASTASIS;
D O I
10.1016/j.bcp.2015.04.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A small set of isoprenoid bisphosphonates ethers has been tested in the K562 chronic myelogenous leukemia cell line to determine their impact on isoprenoid biosynthesis. Five of these compounds inhibit geranylgeranyl diphosphate synthase (GGDPS) with IC50 values below 1 mu M in enzyme assays, but in cells their apparent activity is more varied. In particular, the isomeric C-geranyl-O-prenyl and C-prenyl-O-geranyl bisphosphonates are quite different in their activity with the former consistently demonstrating greater impairment of geranylgeranylation in cells but the latter showing greater impact in the enzyme assays with GGDPS. Together, these findings suggest an organized binding of these inhibitors in the two hydrophobic channels of the geranylgeranyl diphosphate synthase enzyme. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:83 / 92
页数:10
相关论文
共 36 条
[1]   Targeting HMG-CoA reductase with statins in a window-of-opportunity breast cancer trial [J].
Bjarnadottir, Olof ;
Romero, Quinci ;
Bendahl, Par-Ola ;
Jirstrom, Karin ;
Ryden, Lisa ;
Loman, Niklas ;
Uhlen, Mathias ;
Johannesson, Henrik ;
Rose, Carsten ;
Grabau, Dorthe ;
Borgquist, Signe .
BREAST CANCER RESEARCH AND TREATMENT, 2013, 138 (02) :499-508
[2]   THE COOH-TERMINAL DOMAIN OF THE RAP1A (KREV-1) PROTEIN IS ISOPRENYLATED AND SUPPORTS TRANSFORMATION BY AN H-RAS-RAP1A CHIMERIC PROTEIN [J].
BUSS, JE ;
QUILLIAM, LA ;
KATO, K ;
CASEY, PJ ;
SOLSKI, PA ;
WONG, G ;
CLARK, R ;
MCCORMICK, F ;
BOKOCH, GM ;
DER, CJ .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) :1523-1530
[3]   Mechanistic studies of an unprecedented enzyme-catalysed 1,2-phosphono-migration reaction [J].
Chang, Wei-chen ;
Dey, Mishtu ;
Liu, Pinghua ;
Mansoorabadi, Steven O. ;
Moon, Sung-Ju ;
Zhao, Zongbao K. ;
Drennan, Catherine L. ;
Liu, Hung-wen .
NATURE, 2013, 496 (7443) :114-118
[4]   Inhibition of geranylgeranyl diphosphate synthase by bisphosphonates: A crystallographic and computational investigation [J].
Chen, Cammy K. -M. ;
Hudock, Michael P. ;
Zhang, Yonghui ;
Guo, Rey-Ting ;
Cao, Rong ;
No, Joo Hwan ;
Liang, Po-Huang ;
Ko, Tzu-Ping ;
Chang, Tao-Hsin ;
Chang, Shiou-chi ;
Song, Yongcheng ;
Axelson, Jordan ;
Kumar, Anup ;
Wang, Andrew H. -J. ;
Oldfield, Eric .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (18) :5594-5607
[5]  
CORRELL CC, 1994, J BIOL CHEM, V269, P17390
[6]   Statins and cancer prevention [J].
Demierre, MF ;
Higgins, PDR ;
Gruber, SB ;
Hawk, E ;
Lippman, SM .
NATURE REVIEWS CANCER, 2005, 5 (12) :930-942
[7]   Geranylgeranyl diphosphate depletion inhibits breast cancer cell migration [J].
Dudakovic, Amel ;
Tong, Huaxiang ;
Hohl, Raymond J. .
INVESTIGATIONAL NEW DRUGS, 2011, 29 (05) :912-920
[8]   The relationship between the chemistry and biological activity of the bisphosphonates [J].
Ebetino, Frank H. ;
Hogan, Anne-Marie L. ;
Sun, Shuting ;
Tsoumpra, Maria K. ;
Duan, Xuchen ;
Triffitt, James T. ;
Kwaasi, Aaron A. ;
Dunford, James E. ;
Barnett, Bobby L. ;
Oppermann, Udo ;
Lundy, Mark W. ;
Boyde, Alan ;
Kashemirov, Boris A. ;
McKenna, Charles E. ;
Russell, R. Graham G. .
BONE, 2011, 49 (01) :20-33
[9]   PHOSPHONATES AS ANALOGS OF NATURAL PHOSPHATES [J].
ENGEL, R .
CHEMICAL REVIEWS, 1977, 77 (03) :349-367
[10]   RhoA and RhoC proteins promote both cell proliferation and cell invasion of human oesophageal squamous cell carcinoma cell lines in vitro and in vivo [J].
Faried, A. ;
Faried, L. S. ;
Kimura, H. ;
Nakajima, M. ;
Sohda, M. ;
Miyazaki, T. ;
Kato, H. ;
Usman, N. ;
Kuwano, H. .
EUROPEAN JOURNAL OF CANCER, 2006, 42 (10) :1455-1465