Department of Pathology, Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, 740 Hudson Webber Cancer Research Center, 4100 John R St, Detroit, Michigan 48201, USA.
Mol Cancer Ther. 2010 Dec;9(12):3137-44. doi: 10.1158/1535-7163.MCT-10-0642. Epub 2010 Nov 1.
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 malignancies. 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.
针对关键分子的癌症疗法并未如预期那样对大多数常见恶性肿瘤有效。主要挑战包括对这些靶点在患者中的不完全理解和验证、大多数癌症中遗传和表观遗传变化的多样性和复杂性,以及关键信号通路中的冗余和串扰。总之,单一途径靶向方法的应用并不是治疗人类恶性肿瘤的有效方法。为了克服这些障碍,了解关键信号通路之间的分子串扰以及靶向药物如何改变它们非常重要。需要创新的方法,例如了解目标蛋白的全局生理环境以及在不丢失关键分子细节的情况下修饰它们的效果。这些策略将有助于设计针对多方面疾病的新型治疗方法及其组合,其中有效的联合治疗将侧重于改变多个途径,而不是单一蛋白质。基于网络的综合建模和系统生物学已经成为实时了解药物作用机制的有力工具。本文强调了基于网络和系统生物学的策略的重要性,并以我们实验室最近使用奥沙利铂和 MDM2 抑制剂 MI-219 联合治疗遗传复杂且无法治愈的胰腺腺癌为例,提出了一个概念验证。