Proof of Concept: Network and Systems Biology Approaches Aid in the Discovery of Potent Anticancer Drug Combinations

被引:78
作者
Azmi, Asfar S. [1 ]
Wang, Zhiwei [1 ]
Philip, Philip A. [2 ]
Mohammad, Ramzi M. [2 ]
Sarkar, Fazlul H. [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Pathol, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Div Hematol Oncol, Dept Internal Med,Karmanos Canc Inst, Detroit, MI 48201 USA
关键词
PROTEIN-PROTEIN INTERACTION; MDM2; INHIBITOR; CANCER; P53; ACTIVATION; MECHANISMS; PATHWAYS; GENOMICS; GENE;
D O I
10.1158/1535-7163.MCT-10-0642
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer therapies that target key molecules have not fulfilled expected promises for most common malignancies. Major challenges include the incomplete understanding and validation of these targets in patients, the multiplicity and complexity of genetic and epigenetic changes in the majority of cancers, and the redundancies and cross-talk found in key signaling pathways. Collectively, the uses of single-pathway targeted approaches are not effective therapies for human malignances. To overcome these barriers, it is important to understand the molecular cross-talk among key signaling pathways and how they may be altered by targeted agents. Innovative approaches are needed, such as understanding the global physiologic environment of target proteins and the effects of modifying them without losing key molecular details. Such strategies will aid the design of novel therapeutics and their combinations against multifaceted diseases, in which efficacious combination therapies will focus on altering multiple pathways rather than single proteins. Integrated network modeling and systems biology have emerged as powerful tools benefiting our understanding of drug mechanisms of action in real time. This review highlights the significance of the network and systems biology-based strategy and presents a proof of concept recently validated in our laboratory using the example of a combination treatment of oxaliplatin and the MDM2 inhibitor MI-219 in genetically complex and incurable pancreatic adenocarcinoma. Mol Cancer Ther; 9( 12); 3137-44. (C) 2010 AACR.
引用
收藏
页码:3137 / 3144
页数:8
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