Apoptotic cell death induction by F 11782 a novel dual catalytic inhibitor of topoisomerases I and II

被引:6
作者
Etiévant, C [1 ]
Kruczynski, A [1 ]
Barret, JM [1 ]
Perrin, D [1 ]
Hill, BT [1 ]
机构
[1] Ctr Rech Pierre Fabre, Div Cancerol Expt 1, F-81106 Castres 06, France
关键词
F; 11782; topoisomerases; dual inhibitors; apoptosis; P388; leukaemia; in vitro;
D O I
10.1016/S0006-2952(02)01564-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
F11782 (2",3"-bis-pentafluorophenoxyacetyl-4",6"ethylidene-beta-D-glucoside of 4'-phosphate-4'-dimethylepipodophyllotoxin-2N-methyl glucamine salt), is a novel dual catalytic inhibitor of topoisomerases I and 11 characterised by marked in vivo antitumour activity, which also proved cytotoxic and exhibited DNA damaging properties in vitro. Mechanisms associated with this cell killing by F11782 have been examined in P388 leukaemia cells. Treatment with F11782 resulted in a dose-dependent DNA fragmentation coupled with the characteristic morphological features of apoptosis. Apoptosis-inducing concentrations of F11782 induced caspases-3/7 activation accompanied by proteolytic cleavage of poly(ADP-ribose)-polymerase, which could be inhibited by the caspase inhibitor acetyl-Asp-Glu-Val-Asp-aldehyde. In addition, F11782-induced apoptosis in P388 cells was associated with an increased expression of the pro-apototic Bax protein, without significant changes in the level of the anti-apoptotic Bcl-2 protein, and with modification at the mitochondrial membrane function. These results indicate that F11782 leads to apoptosis through a caspase-3/7 dependent mechanism and suggest that the so-called "mitochondrial pathway" is implicated in F11782-induced apoptosis in P388 cells. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:755 / 763
页数:9
相关论文
共 32 条
[11]   The human decatenation checkpoint [J].
Deming, PB ;
Cistulli, CA ;
Zhao, H ;
Graves, PR ;
Piwnica-Worms, H ;
Paules, RS ;
Downes, CS ;
Kaufmann, WK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12044-12049
[12]   F 11782, a dual inhibitor of topoisomerases I and II with an original mechanism of action in vitro, and markedly superior in vivo antitumour activity, relative to three other dual topoisomerase inhibitors, intoplicin, aclarubicin and TAS-103 [J].
Etiévant, C ;
Kruczynski, A ;
Barret, JM ;
Perrin, D ;
van Hille, B ;
Guminski, Y ;
Hill, BT .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2000, 46 (02) :101-113
[13]  
Garcia-Bermejo L, 1998, J CELL SCI, V111, P637
[14]  
Gatto B, 1999, CURR PHARM DESIGN, V5, P195
[15]   The biochemistry of apoptosis [J].
Hengartner, MO .
NATURE, 2000, 407 (6805) :770-776
[16]   Protein tyrosine phosphatase activities are involved in apoptotic cancer cell death induced by GL331, a new homolog of etoposide [J].
Huang, TS ;
Shu, CH ;
Shih, YL ;
Huang, HC ;
Su, YC ;
Chao, Y ;
Yang, WK ;
WhangPeng, J .
CANCER LETTERS, 1996, 110 (1-2) :77-85
[17]  
ISHIDA R, 1991, CANCER RES, V51, P4909
[18]  
KAUFMANN SH, 1993, CANCER RES, V53, P3976
[19]   Cell death induced by topoisomerase-targeted drugs: more questions than answers [J].
Kaufmann, SH .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1998, 1400 (1-3) :195-211
[20]  
Kluza J, 2000, CANCER RES, V60, P4077