RPR112378 and RPR115781: Two representatives of a new family of microtubule assembly inhibitors

被引:45
作者
Combeau, C [1 ]
Provost, J [1 ]
Lancelin, F [1 ]
Tournoux, Y [1 ]
Prod'homme, F [1 ]
Herman, F [1 ]
Lavelle, F [1 ]
Leboul, J [1 ]
Vuilhorgne, M [1 ]
机构
[1] Rhone Poulenc Rorer SA, Ctr Rech Vitry Alfortville, Dept Oncol, F-94403 Vitry, France
关键词
D O I
10.1124/mol.57.3.553
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A screening program aimed at the discovery of new antimicrotubule agents yielded RPR112378 and RPR115781, two natural compounds extracted from the Indian plant Ottelia alismoides. We report their isolation, structural determination, and mechanisms of action. RPR112378 is an efficient inhibitor of tubulin polymerization (IC50 = 1.2 mu M) and is able to disassemble preformed microtubules. Regarding tubulin activity, RPR115781 is 5-fold less active than RPR112378. Tubulin-RPR112378 complexes, when isolated by gel filtration, were able to block further tubulin addition to growing microtubules, a mechanism that accounts for the substoichiometric effect of the drug. RPR112378 was found to prevent colchicine binding but not vinblastine binding to tubulin. Although colchicine binding is known to induce an increase of tubulin GTPase activity, no such increase was observed with RPR112378. We show that RPR112378 is a highly cytotoxic compound and that RPR115781 is 10,000-fold less active as an inhibitor of KB cell growth. Part of the cytotoxicity of RPR112378 is probably caused by a reaction of addition with sulfhydryl groups, an observation that has not been made with RPR115781. In conclusion, these molecules represent a new class of inhibitors of microtubule assembly with potential therapeutic value.
引用
收藏
页码:553 / 563
页数:11
相关论文
共 42 条
[1]   MECHANISM OF COLCHICINE BINDING TO TUBULIN - TOLERANCE OF SUBSTITUENTS IN RING-C' OF BIPHENYL ANALOGS [J].
ANDREU, JM ;
GORBUNOFF, MJ ;
MEDRANO, FJ ;
ROSSI, M ;
TIMASHEFF, SN .
BIOCHEMISTRY, 1991, 30 (15) :3777-3786
[2]   Otteliones A and B:: Potently cytotoxic 4-methylene-2-cyclohexenones from Ottelia alismoides [J].
Ayyad, SEN ;
Judd, AS ;
Shier, WT ;
Hoye, TR .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (23) :8102-8106
[3]   MECHANISM OF ACTION OF THE ANTIMITOTIC DRUG 2,4-DICHLOROBENZYL THIOCYANATE - ALKYLATION OF SULFHYDRYL GROUP(S) OF BETA-TUBULIN [J].
BAI, RL ;
DUANMU, C ;
HAMEL, E .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 994 (01) :12-20
[4]   IDENTIFICATION OF THE CYSTEINE RESIDUE OF BETA-TUBULIN ALKYLATED BY THE ANTIMITOTIC AGENT 2,4-DICHLOROBENZYL THIOCYANATE, FACILITATED BY SEPARATION OF THE PROTEIN SUBUNITS OF TUBULIN BY HYDROPHOBIC COLUMN CHROMATOGRAPHY [J].
BAI, RL ;
LIN, CM ;
NGUYEN, NY ;
LIU, TY ;
HAMEL, E .
BIOCHEMISTRY, 1989, 28 (13) :5606-5612
[5]  
BOLLAG DM, 1995, CANCER RES, V55, P2325
[6]   MICROTUBULE ELONGATION AND GUANOSINE 5'-TRIPHOSPHATE HYDROLYSIS - ROLE OF GUANINE-NUCLEOTIDES IN MICROTUBULE DYNAMICS [J].
CARLIER, MF ;
DIDRY, D ;
PANTALONI, D .
BIOCHEMISTRY, 1987, 26 (14) :4428-4437
[7]  
DAVIDPFEUTY T, 1979, J BIOL CHEM, V254, P1696
[8]   SPATIAL SEPARATION OF THE 2 ESSENTIAL THIOL-GROUPS AND THE BINDING-SITE OF THE EXCHANGEABLE GTP IN BRAIN TUBULIN A SPIN LABEL STUDY [J].
DEINUM, J ;
WALLIN, M ;
LAGERCRANTZ, C .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 671 (01) :1-8
[9]   VINBLASTINE SUPPRESSES DYNAMICS OF INDIVIDUAL MICROTUBULES IN LIVING INTERPHASE CELLS [J].
DHAMODHARAN, R ;
JORDAN, MA ;
THROWER, D ;
WILSON, L ;
WADSWORTH, P .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (09) :1215-1229
[10]   TURBIDIMETRIC STUDIES OF INVITRO ASSEMBLY AND DISASSEMBLY OF PORCINE NEUROTUBULES [J].
GASKIN, F ;
CANTOR, CR ;
SHELANSKI, ML .
JOURNAL OF MOLECULAR BIOLOGY, 1974, 89 (04) :737-+