Deep learning of pharmacogenomics resources: moving towards precision oncology

被引:35
|
作者
Chiu, Yu-Chiao [2 ]
Chen, Hung-I Harry [1 ,3 ]
Gorthi, Aparna [4 ]
Mostavi, Milad [3 ]
Zheng, Siyuan [5 ]
Huang, Yufei [3 ]
Chen, Yidong [5 ,6 ]
机构
[1] NGM Biopharmaceut Inc, San Francisco, CA 94080 USA
[2] Univ Texas Hlth San Antonio, Greehey Childrens Canc Res Inst, San Antonio, TX USA
[3] Univ Texas San Antonio, Dept Elect & Comp Engn, San Antonio, TX USA
[4] Greehey Childrens Canc Res Inst, San Antonio, TX USA
[5] Univ Texas Hlth San Antonio, Greehey Childrens Canc Res Inst, Dept Populat Hlth Sci, San Antonio, TX USA
[6] Univ Texas Hlth San Antonio, Greehey Childrens Canc Res Inst, Computat Biol & Bioinformat, San Antonio, TX USA
基金
美国国家卫生研究院;
关键词
deep learning; precision oncology; pharmacogenomics; cancer; drug discovery; CANCER-CELL LINES; DRUG DISCOVERY; MOLECULAR PHARMACOLOGY; NEURAL-NETWORK; BIG DATA; GENE; GENOME; EXPRESSION; DATABASE; SENSITIVITY;
D O I
10.1093/bib/bbz144
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The recent accumulation of cancer genomic data provides an opportunity to understand how a tumor's genomic characteristics can affect its responses to drugs. This field, called pharmacogenomics, is a key area in the development of precision oncology. Deep learning (DL) methodology has emerged as a powerful technique to characterize and learn from rapidly accumulating pharmacogenomics data. We introduce the fundamentals and typical model architectures of DL. We review the use of DL in classification of cancers and cancer subtypes (diagnosis and treatment stratification of patients), prediction of drug response and drug synergy for individual tumors (treatment prioritization for a patient), drug repositioning and discovery and the study of mechanism/mode of action of treatments. For each topic, we summarize current genomics and pharmacogenomics data resources such as pan-cancer genomics data for cancer cell lines (CCLs) and tumors, and systematic pharmacologic screens of CCLs. By revisiting the published literature, including our in-house analyses, we demonstrate the unprecedented capability of DL enabled by rapid accumulation of data resources to decipher complex drug response patterns, thus potentially improving cancer medicine. Overall, this review provides an in-depth summary of state-of-the-art DL methods and up-to-date pharmacogenomics resources and future opportunities and challenges to realize the goal of precision oncology.
引用
收藏
页码:2066 / 2083
页数:18
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