Network-based machine learning in colorectal and bladder organoid models predicts anti-cancer drug efficacy in patients

被引:143
作者
Kong, JungHo [1 ]
Lee, Heetak [1 ]
Kim, Donghyo [1 ]
Han, Seong Kyu [1 ]
Ha, Doyeon [1 ]
Shin, Kunyoo [1 ,2 ]
Kim, Sanguk [1 ,2 ]
机构
[1] Pohang Univ Sci & Technol, Dept Life Sci, Pohang 790784, South Korea
[2] Yonsei Univ, Inst Convergence Sci, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
BH3-ONLY PROTEINS; CANCER; SENSITIVITY; 5-FLUOROURACIL; MECHANISMS; SIGNATURES; GENOMICS; REVEALS; BASAL;
D O I
10.1038/s41467-020-19313-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cancer patient classification using predictive biomarkers for anti-cancer drug responses is essential for improving therapeutic outcomes. However, current machine-learning-based predictions of drug response often fail to identify robust translational biomarkers from preclinical models. Here, we present a machine-learning framework to identify robust drug biomarkers by taking advantage of network-based analyses using pharmacogenomic data derived from three-dimensional organoid culture models. The biomarkers identified by our approach accurately predict the drug responses of 114 colorectal cancer patients treated with 5-fluorouracil and 77 bladder cancer patients treated with cisplatin. We further confirm our biomarkers using external transcriptomic datasets of drug-sensitive and -resistant isogenic cancer cell lines. Finally, concordance analysis between the transcriptomic biomarkers and independent somatic mutation-based biomarkers further validate our method. This work presents a method to predict cancer patient drug responses using pharmacogenomic data derived from organoid models by combining the application of gene modules and network-based approaches. Cancer patient classification using predictive biomarkers for anti-cancer drug responses is essential for improving therapeutic outcomes. Here, the authors present a machine-learning framework to identify robust drug biomarkers by taking advantage of network-based analyses using pharmacogenomic data.
引用
收藏
页数:13
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