4.7 Article

Systems Medicine Design based on Systems Biology Approaches and Deep Neural Network for Gastric Cancer

Publisher

IEEE COMPUTER SOC
DOI: 10.1109/TCBB.2021.3095369

Keywords

Drugs; Cancer; Biomarkers; Regulation; Proteins; Systems biology; Databases; Machine learning; Modeling techniques; Biology and genetics; Molecular biology

Funding

  1. Ministry of Science and Technology of Taiwan [MOST 1072221-E-007-112-MY3]

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This study proposes a systematic approach to investigate the molecular progression mechanisms of gastric cancer and identifies critical biomarkers and corresponding drugs. By utilizing big database mining, system modeling, and deep learning techniques, the study successfully reveals the progression of gastric cancer and suggests potential multi-target drugs.
Gastric cancer (GC) is the third leading cause of cancer death in the world. It is associated with the stimulation of microenvironment, aberrant epigenetic modification, and chronic inflammation. However, few researches discuss the GC molecular progression mechanisms from the perspective of the system level. In this study, we proposed a systems medicine design procedure to identify essential biomarkers and find corresponding drugs for GC. At first, we did big database mining to construct candidate protein-protein interaction network (PPIN) and candidate gene regulation network (GRN). Second, by leveraging the next-generation sequencing (NGS) data, we performed system modeling and applied system identification and model selection to obtain real genome-wide genetic and epigenetic networks (GWGENs). To make the real GWGENs easy to analyze, the principal network projection method was used to extract the core signaling pathways denoted by KEGG pathways. Subsequently, based on the identified biomarkers, we trained a deep neural network of drug-target interaction (DeepDTI) with supervised learning and filtered our candidate drugs considering drug regulation ability and drug sensitivity. With the proposed systematic strategy, we not only shed the light on the progression of GC but also suggested potential multiple-molecule drugs efficiently.

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