Chemotherapy and signaling How can targeted therapies supercharge cytotoxic agents?

被引:80
作者
Bagnyukova, Tetyana [1 ]
Serebriiskii, Ilya G. [1 ]
Zhou, Yan [1 ]
Hopper-Borge, Elizabeth A. [1 ]
Golemis, Erica A. [1 ]
Astsaturov, Igor [1 ]
机构
[1] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
关键词
chemotherapy; resistance; targeted therapy; RNAi screen; integrative biology; DNA damage; synthetic lethality; EPITHELIAL-MESENCHYMAL TRANSITIONS; CELL LUNG-CANCER; HIGH-DOSE CHEMOTHERAPY; DOUBLE-STRAND BREAKS; SYNTHETIC LETHAL; POLY(ADP-RIBOSE) POLYMERASE-1; DNA-DAMAGE; STEM-CELLS; TRANSCRIPTION FACTOR; ACQUIRED-RESISTANCE;
D O I
10.4161/cbt.10.9.13738
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, oncologists have begun to conclude that chemotherapy has reached a plateau of efficacy as a primary treatment modality, even if toxicity can be effectively controlled. Emerging specific inhibitors of signaling and metabolic pathways (i.e., targeted agents) contrast with traditional chemotherapy drugs in that the latter primarily interfere with the DNA biosynthesis and the cell replication machinery. In an attempt to improve on the efficacy, combination of targeted drugs with conventional chemotherapeutics has become a routine way of testing multiple new agents in early phase clinical trials. This review discusses the recent advances including integrative systematic biology and RNAi approaches to counteract the chemotherapy resistance and to buttress the selectivity, efficacy and personalization of anticancer drug therapy.
引用
收藏
页码:843 / 857
页数:15
相关论文
共 199 条
[1]   Taxanes: Microtubule and Centrosome Targets, and Cell Cycle Dependent Mechanisms of Action [J].
Abal, M. ;
Andreu, J. M. ;
Barasoain, I. .
CURRENT CANCER DRUG TARGETS, 2003, 3 (03) :193-203
[2]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]   The ERCC1/XPF endonuclease is required for completion of homologous recombination at DNA replication forks stalled by inter-strand cross-links [J].
Al-Minawi, Ali Z. ;
Lee, Yin-Fai ;
Hakansson, Daniel ;
Johansson, Fredrik ;
Lundin, Cecilia ;
Saleh-Gohari, Nasrollah ;
Schultz, Niklas ;
Jenssen, Dag ;
Bryant, Helen E. ;
Meuth, Mark ;
Hinz, John M. ;
Helleday, Thomas .
NUCLEIC ACIDS RESEARCH, 2009, 37 (19) :6400-6413
[4]  
ALBERTS SR, 2010, J CLIN ONCOL, V18
[5]   Initial Safety Report of NSABP C-08: A Randomized Phase III Study of Modified FOLFOX6 With or Without Bevacizumab for the Adjuvant Treatment of Patients With Stage II or III Colon Cancer [J].
Allegra, Carmen J. ;
Yothers, Greg ;
O'Connell, Michael J. ;
Sharif, Saima ;
Colangelo, Linda H. ;
Lopa, Samia H. ;
Petrelli, Nicholas J. ;
Goldberg, Richard M. ;
Atkins, James N. ;
Seay, Thomas E. ;
Fehrenbacher, Louis ;
O'Reilly, Seamus ;
Chu, Luis ;
Azar, Catherine A. ;
Wolmark, Norman .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (20) :3385-3390
[6]   Mouse double minute antagonist Nutlin-3a enhances chemotherapy-induced apoptosis in cancer cells with mutant p53 by activating E2F1 [J].
Ambrosini, G. ;
Sambol, E. B. ;
Carvajal, D. ;
Vassilev, L. T. ;
Singer, S. ;
Schwartz, G. K. .
ONCOGENE, 2007, 26 (24) :3473-3481
[7]   Evolvable signaling networks of receptor tyrosine kinases: relevance of robustness to malignancy and to cancer therapy [J].
Amit, Ido ;
Wides, Ron ;
Yarden, Yosef .
MOLECULAR SYSTEMS BIOLOGY, 2007, 3 (1)
[8]  
[Anonymous], ONCOGENE
[9]   Downregulation of XPF-ERCC1 enhances cisplatin efficacy in cancer cells [J].
Arora, Sanjeevani ;
Kothandapani, Anbarasi ;
Tillison, Kristin ;
Kalman-Maltese, Vivian ;
Patrick, Steve M. .
DNA REPAIR, 2010, 9 (07) :745-753
[10]   Keeping checkpoint kinases in line: new selective inhibitors in clinical trials [J].
Ashwell, Susan ;
Janetka, James W. ;
Zabludoff, Sonya .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2008, 17 (09) :1331-1340