Your browser doesn't support javascript.
loading
Harnessing Human Microphysiology Systems as Key Experimental Models for Quantitative Systems Pharmacology.
Taylor, D Lansing; Gough, Albert; Schurdak, Mark E; Vernetti, Lawrence; Chennubhotla, Chakra S; Lefever, Daniel; Pei, Fen; Faeder, James R; Lezon, Timothy R; Stern, Andrew M; Bahar, Ivet.
Afiliação
  • Taylor DL; University of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA. dltaylor@pitt.edu.
  • Gough A; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA. dltaylor@pitt.edu.
  • Schurdak ME; University of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
  • Vernetti L; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Chennubhotla CS; University of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
  • Lefever D; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Pei F; University of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
  • Faeder JR; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Lezon TR; University of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
  • Stern AM; Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Bahar I; University of Pittsburgh Drug Discovery Institute, Pittsburgh, PA, USA.
Handb Exp Pharmacol ; 260: 327-367, 2019.
Article em En | MEDLINE | ID: mdl-31201557
Two technologies that have emerged in the last decade offer a new paradigm for modern pharmacology, as well as drug discovery and development. Quantitative systems pharmacology (QSP) is a complementary approach to traditional, target-centric pharmacology and drug discovery and is based on an iterative application of computational and systems biology methods with multiscale experimental methods, both of which include models of ADME-Tox and disease. QSP has emerged as a new approach due to the low efficiency of success in developing therapeutics based on the existing target-centric paradigm. Likewise, human microphysiology systems (MPS) are experimental models complementary to existing animal models and are based on the use of human primary cells, adult stem cells, and/or induced pluripotent stem cells (iPSCs) to mimic human tissues and organ functions/structures involved in disease and ADME-Tox. Human MPS experimental models have been developed to address the relatively low concordance of human disease and ADME-Tox with engineered, experimental animal models of disease. The integration of the QSP paradigm with the use of human MPS has the potential to enhance the process of drug discovery and development.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacologia / Biologia Computacional / Biologia de Sistemas Limite: Animals / Humans Idioma: En Revista: Handb Exp Pharmacol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacologia / Biologia Computacional / Biologia de Sistemas Limite: Animals / Humans Idioma: En Revista: Handb Exp Pharmacol Ano de publicação: 2019 Tipo de documento: Article