Literature DB >> 29803319

Genetic-Driven Druggable Target Identification and Validation.

Matteo Floris1, Stefania Olla2, David Schlessinger3, Francesco Cucca4.   

Abstract

Choosing the right biological target is the critical primary decision for the development of new drugs. Systematic genetic association testing of both human diseases and quantitative traits, along with resultant findings of coincident associations between them, is becoming a powerful approach to infer drug targetable candidates and generate in vitro tests to identify compounds that can modulate them therapeutically. Here, we discuss opportunities and challenges, and infer criteria for the optimal use of genetic findings in the drug discovery pipeline.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  coincident genetic associations; drug discovery; druggability; quantitative phenotypes; therapeutic targets

Mesh:

Year:  2018        PMID: 29803319      PMCID: PMC6088790          DOI: 10.1016/j.tig.2018.04.004

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  86 in total

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Journal:  Nat Genet       Date:  2003-06       Impact factor: 38.330

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Authors:  Dac-Trung Nguyen; Stephen Mathias; Cristian Bologa; Soren Brunak; Nicolas Fernandez; Anna Gaulton; Anne Hersey; Jayme Holmes; Lars Juhl Jensen; Anneli Karlsson; Guixia Liu; Avi Ma'ayan; Geetha Mandava; Subramani Mani; Saurabh Mehta; John Overington; Juhee Patel; Andrew D Rouillard; Stephan Schürer; Timothy Sheils; Anton Simeonov; Larry A Sklar; Noel Southall; Oleg Ursu; Dusica Vidovic; Anna Waller; Jeremy Yang; Ajit Jadhav; Tudor I Oprea; Rajarshi Guha
Journal:  Nucleic Acids Res       Date:  2016-11-29       Impact factor: 16.971

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Journal:  Nat Genet       Date:  2015-09-14       Impact factor: 38.330

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Review 5.  Knowledge-based approaches to drug discovery for rare diseases.

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6.  Druggable hot spots in trypanothione reductase: novel insights and opportunities for drug discovery revealed by DRUGpy.

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8.  Complex genetic signatures in immune cells underlie autoimmunity and inform therapy.

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9.  APOE E2/E2 Is Associated with Slower Rate of Cognitive Decline with Age.

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