Harnessing Big Data for Systems Pharmacology. Review uri icon

Overview

abstract

  • Systems pharmacology aims to holistically understand mechanisms of drug actions to support drug discovery and clinical practice. Systems pharmacology modeling (SPM) is data driven. It integrates an exponentially growing amount of data at multiple scales (genetic, molecular, cellular, organismal, and environmental). The goal of SPM is to develop mechanistic or predictive multiscale models that are interpretable and actionable. The current explosions in genomics and other omics data, as well as the tremendous advances in big data technologies, have already enabled biologists to generate novel hypotheses and gain new knowledge through computational models of genome-wide, heterogeneous, and dynamic data sets. More work is needed to interpret and predict a drug response phenotype, which is dependent on many known and unknown factors. To gain a comprehensive understanding of drug actions, SPM requires close collaborations between domain experts from diverse fields and integration of heterogeneous models from biophysics, mathematics, statistics, machine learning, and semantic webs. This creates challenges in model management, model integration, model translation, and knowledge integration. In this review, we discuss several emergent issues in SPM and potential solutions using big data technology and analytics. The concurrent development of high-throughput techniques, cloud computing, data science, and the semantic web will likely allow SPM to be findable, accessible, interoperable, reusable, reliable, interpretable, and actionable.

publication date

  • October 13, 2016

Research

keywords

  • Data Interpretation, Statistical
  • Databases, Factual
  • Pharmacology, Clinical
  • Systems Biology

Identity

PubMed Central ID

  • PMC5626567

Scopus Document Identifier

  • 85009135184

Digital Object Identifier (DOI)

  • 10.1146/annurev-pharmtox-010716-104659

PubMed ID

  • 27814027

Additional Document Info

volume

  • 57