Feedback analysis identifies a combination target for overcoming adaptive resistance to targeted cancer therapy

被引:14
作者
Park, Sang-Min [1 ]
Hwang, Chae Young [1 ]
Choi, Jihye [1 ]
Joung, Chang Young [1 ]
Cho, Kwang-Hyun [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Lab Syst Biol & Bioinspired Engn, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
MEK INHIBITION; SYSTEMS BIOLOGY; NETWORKS; DYNAMICS; BRAF; PATHWAY; SRC; KINOME; ENCYCLOPEDIA; ACTIVATION;
D O I
10.1038/s41388-020-1255-y
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
Targeted drugs aim to treat cancer by directly inhibiting oncogene activity or oncogenic pathways, but drug resistance frequently emerges. Due to the intricate dynamics of cancer signaling networks, which contain complex feedback regulations, cancer cells can rewire these networks to adapt to and counter the cytotoxic effects of a drug, thereby limiting the efficacy of targeted therapies. To identify a combinatorial drug target that can overcome such a limitation, we developed a Boolean network simulation and analysis framework and applied this approach to a large-scale signaling network of colorectal cancer with integrated genomic information. We discovered Src as a critical combination drug target that can overcome the adaptive resistance to the targeted inhibition of mitogen-activated protein kinase pathway by blocking the essential feedback regulation responsible for resistance. The proposed framework is generic and can be widely used to identify drug targets that can overcome adaptive resistance to targeted therapies.
引用
收藏
页码:3803 / 3820
页数:18
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