Ecteinascidin-743 (ET-743), a natural marine compound, with a unique mechanism of action

被引:233
作者
Erba, E
Bergamaschi, D
Bassano, L
Damia, G
Ronzoni, S
Faircloth, GT
D'Incalci, M
机构
[1] Ist Ric Farmacol Mario Negri, Dept Oncol, I-20157 Milan, Italy
[2] Pharma Mar USA Inc, Cambridge, MA 02139 USA
关键词
ecteinascidin-743; natural product; DNA-interacting drug; cell cycle; DNA repair;
D O I
10.1016/S0959-8049(00)00357-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mode of action of Ecteinascidin-743 (ET-743), a marine tetrahydroisoquinoline alkaloid isolated from Ecteinascidia turbinata. which has shown very potent antitumour activity in preclinical systems and encouraging results in Phase I clinical trials was investigated at a cellular level. Both SW620 and LoVo human intestinal carcinoma cell lines exposed For 1 h to ET-743 progress through S phase more slowly than control cells and then accumulate in the G(2)M phase. The sensitivity to ET-743 of G(1) synchronised cells was much higher than that of cells synchronised in S phase and even higher than that of cells synchronised in G(2)M. ET-743 concentrations up to Four times higher than the IC50 value caused no detectable DNA breaks or DNA-protein cross-links as assessed by alkaline elution techniques. ET-743 induced a significant increase in p53 levels in cell lines expressing wild-type (wt) (p53). However, the p53 status does not appear to be related to the ET-743 cytotoxic activity as demonstrated by comparing the drug sensitivity in p53 (-/-) or (+/+) mouse embryo fibroblasts and in A2780 ovarian cancer cells or the A2780/CX3 sub-line transfected with a dominant-negative mutant TP53. The cytotoxic potency of ET-743 was comparatively evaluated in CHO cell lines proficient or deficient in nucleotide excision repair (NER), and it nas found that ET-743 was approximately 7-8 times less active in ERCC3/XPB and ERCC1-deficient cells than control cells. The findings that G(1) phase cells are hypersensitive and that NER-deficient cells are resistant to ET-743 indicate that the mode of action of ET-743 is unique and different from that of other DNA-interacting drugs. (C) 2001 Published by Elsevier Science Ltd.
引用
收藏
页码:97 / 105
页数:9
相关论文
共 32 条
[1]  
Bonsing BA, 1997, CYTOMETRY, V28, P11, DOI 10.1002/(SICI)1097-0320(19970501)28:1<11::AID-CYTO2>3.3.CO
[2]  
2-H
[3]   DNA SEQUENCE-SPECIFIC ADENINE ALKYLATION BY THE NOVEL ANTITUMOR DRUG TALLIMUSTINE (FCE-24517), A BENZOYL NITROGEN-MUSTARD DERIVATIVE OF DISTAMYCIN [J].
BROGGINI, M ;
COLEY, HM ;
MONGELLI, N ;
PESENTI, E ;
WYATT, MD ;
HARTLEY, JA ;
DINCALCI, M .
NUCLEIC ACIDS RESEARCH, 1995, 23 (01) :81-87
[4]  
CVITKOVIC E, 1999, P ASCO, V18, pA180
[5]  
Damia G, 1996, INT J CANCER, V66, P779, DOI 10.1002/(SICI)1097-0215(19960611)66:6<779::AID-IJC12>3.0.CO
[6]  
2-Z
[7]   Cisplatin and adriamycin resistance are associated with MutL alpha and mismatch repair deficiency in an ovarian tumor cell line [J].
Drummond, JT ;
Anthoney, A ;
Brown, R ;
Modrich, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (33) :19645-19648
[8]   COMPARISON OF CELL-CYCLE PHASE PERTURBATIONS INDUCED BY THE DNA-MINOR-GROOVE ALKYLATOR TALLIMUSTINE AND BY MELPHALAN IN THE SW626 CELL-LINE [J].
ERBA, E ;
MASCELLANI, E ;
PIFFERI, A ;
DINCALCI, M .
INTERNATIONAL JOURNAL OF CANCER, 1995, 62 (02) :170-175
[9]  
Faretta M, 1998, CYTOMETRY, V31, P53
[10]  
Fink D, 1997, CANCER RES, V57, P1841