Cellular response to etoposide treatment

被引:194
作者
Montecucco, Alessandra [1 ]
Biamonti, Giuseppe [1 ]
机构
[1] CNR, Ist Genet Mol, I-27100 Pavia, Italy
关键词
etoposide; anticancer drugs; topoisomerase poisons; DNA topoisomerase; DNA replication; replication factories; PCNA; DNA repair; double-stranded breaks; DNA damage checkpoint; ATR; ATM; cell cycle; apoptosis; chromatin; alternative splicing;
D O I
10.1016/j.canlet.2006.11.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Etoposide is a potent anti-tumor drug that belongs to the class of topoisomerase poisons. Although its molecular target, i.e. DNA topoisomerase II, has been identified more than 20 years ago, the cellular response to etoposide is still poorly understood. The cytotoxicity of the drug stems from its ability to stabilize a covalent complex between DNA topoisomerase II and DNA that results in a high level of DNA damage. Here, we review the present knowledge about the strategy used by the cells to deal with the etoposide-induced DNA damage. New and unanticipated effects of topoisomerase II poisoning on cell metabolism are recently emerging, among which the ability to activate cell cycle checkpoint pathways and to affect gene expression at different levels, including chromatin remodeling and alternative splicing of gene transcripts. The elucidation of the effects of etoposide on cell metabolism will increase our ability to exploit this drug in cancer therapy and will expand our comprehension of the cancerous cell. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 18
页数:10
相关论文
共 61 条
[1]   Differential impact of diverse anticancer chemotherapeutics on the Cdc25A-degradation checkpoint pathway [J].
Agner, J ;
Falck, J ;
Lukas, J ;
Bartek, J .
EXPERIMENTAL CELL RESEARCH, 2005, 302 (02) :162-169
[2]   Checking on DNA damage in S phase [J].
Bartek, J ;
Lukas, C ;
Lukas, J .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (10) :792-804
[3]   DNA replication in eukaryotic cells [J].
Bell, SP ;
Dutta, A .
ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 :333-374
[4]   A two-drug model for etoposide action against human topoisomerase IIα [J].
Bromberg, KD ;
Burgin, AB ;
Osheroff, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (09) :7406-7412
[5]   Topoisomerase II etoposide interactions direct the formation of drug-induced enzyme-DNA cleavage complexes [J].
Burden, DA ;
Kingma, PS ;
FroelichAmmon, SJ ;
Bjornsti, MA ;
Patchan, MW ;
Thompson, RB ;
Osheroff, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) :29238-29244
[6]  
CALDECOTT K, 1990, CANCER RES, V50, P5778
[7]   HYPERSENSITIVITY OF LYMPHOBLASTOID LINES DERIVED FROM ATAXIA-TELANGIECTASIA PATIENTS TO THE INDUCTION OF CHROMOSOMAL-ABERRATIONS BY ETOPOSIDE (VP-16) [J].
CAPOROSSI, D ;
PORFIRIO, B ;
NICOLETTI, B ;
PALITTI, F ;
DEGRASSI, F ;
DESALVIA, R ;
TANZARELLA, C .
MUTATION RESEARCH, 1993, 290 (02) :265-272
[8]   DNA topoisomerases: Structure, function, and mechanism [J].
Champoux, JJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :369-413
[9]   Repair of DNA covalently linked to protein [J].
Connelly, JC ;
Leach, DRF .
MOLECULAR CELL, 2004, 13 (03) :307-316
[10]   An ATR- and Cdc7-dependent DNA damage checkpoint that inhibits initiation of DNA replication [J].
Costanzo, V ;
Shechter, D ;
Lupardus, PJ ;
Cimprich, KA ;
Gottesman, M ;
Gautier, J .
MOLECULAR CELL, 2003, 11 (01) :203-213