Network-based approaches for drug response prediction and targeted therapy development in cancer

被引:20
|
作者
Dorel, Mathurin [1 ,2 ,3 ,4 ]
Barillot, Emmanuel [1 ,2 ,3 ]
Zinovyev, Andrei [1 ,2 ,3 ]
Kuperstein, Irma [1 ,2 ,3 ]
机构
[1] Inst Curie, F-75248 Paris, France
[2] INSERM, U900, F-75248 Paris, France
[3] Mines ParisTech, F-77300 Fontainebleau, France
[4] Ecole Normale Super, F-75231 Paris, France
关键词
Signaling network; High-throughput data; Cancer; Drug response; Synthetic lethality; Targeted treatment; SET ENRICHMENT ANALYSIS; PATHWAY ANALYSIS; DISCOVERY; DATABASE; COMBINATIONS; SENSITIVITY; INTEGRATION; INHIBITION; RESISTANCE; NAVICELL;
D O I
10.1016/j.bbrc.2015.06.094
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Signaling pathways implicated in cancer create a complex network with numerous regulatory loops and redundant pathways. This complexity explains frequent failure of one-drug-one-target paradigm of treatment, resulting in drug resistance in patients. To overcome the robustness of cell signaling network, cancer treatment should be extended to a combination therapy approach. Integrating and analyzing patient high-throughput data together with the information about biological signaling machinery may help deciphering molecular patterns specific to each patient and finding the best combinations of candidates for therapeutic targeting. We review state of the art in the field of targeted cancer medicine from the computational systems biology perspective. We summarize major signaling network resources and describe their characteristics with respect to applicability for drug response prediction and intervention targets suggestion. Thus discuss methods for prediction of drug sensitivity and intervention combinations using signaling networks together with high-throughput data. Gradual integration of these approaches into clinical routine will improve prediction of response to standard treatments and adjustment of intervention schemes. (C) 2015 Elsevier Inc. All rights reserved.
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页码:386 / 391
页数:6
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