Molecular Phenotyping Combines Molecular Information, Biological Relevance, and Patient Data to Improve Productivity of Early Drug Discovery. Issue 5 (18th May 2017)
- Record Type:
- Journal Article
- Title:
- Molecular Phenotyping Combines Molecular Information, Biological Relevance, and Patient Data to Improve Productivity of Early Drug Discovery. Issue 5 (18th May 2017)
- Main Title:
- Molecular Phenotyping Combines Molecular Information, Biological Relevance, and Patient Data to Improve Productivity of Early Drug Discovery
- Authors:
- Drawnel, Faye Marie
Zhang, Jitao David
Küng, Erich
Aoyama, Natsuyo
Benmansour, Fethallah
Araujo Del Rosario, Andrea
Jensen Zoffmann, Sannah
Delobel, Frédéric
Prummer, Michael
Weibel, Franziska
Carlson, Coby
Anson, Blake
Iacone, Roberto
Certa, Ulrich
Singer, Thomas
Ebeling, Martin
Prunotto, Marco - Abstract:
- Summary: Today, novel therapeutics are identified in an environment which is intrinsically different from the clinical context in which they are ultimately evaluated. Using molecular phenotyping and an in vitro model of diabetic cardiomyopathy, we show that by quantifying pathway reporter gene expression, molecular phenotyping can cluster compounds based on pathway profiles and dissect associations between pathway activities and disease phenotypes simultaneously. Molecular phenotyping was applicable to compounds with a range of binding specificities and triaged false positives derived from high-content screening assays. The technique identified a class of calcium-signaling modulators that can reverse disease-regulated pathways and phenotypes, which was validated by structurally distinct compounds of relevant classes. Our results advocate for application of molecular phenotyping in early drug discovery, promoting biological relevance as a key selection criterion early in the drug development cascade. Graphical Abstract: Highlights: Molecular phenotyping stratifies compounds based on pathway profiles Molecular phenotyping detects false-positive hits in a phenotypic screen Molecular phenotyping correlates pathway activity patterns with phenotypic readouts Molecular phenotyping can be powered by preclinical and clinical data Abstract : Drawnel and Zhang et al. show that quantitative mRNA sequencing of pathway reporter genes can be powered by translational information andSummary: Today, novel therapeutics are identified in an environment which is intrinsically different from the clinical context in which they are ultimately evaluated. Using molecular phenotyping and an in vitro model of diabetic cardiomyopathy, we show that by quantifying pathway reporter gene expression, molecular phenotyping can cluster compounds based on pathway profiles and dissect associations between pathway activities and disease phenotypes simultaneously. Molecular phenotyping was applicable to compounds with a range of binding specificities and triaged false positives derived from high-content screening assays. The technique identified a class of calcium-signaling modulators that can reverse disease-regulated pathways and phenotypes, which was validated by structurally distinct compounds of relevant classes. Our results advocate for application of molecular phenotyping in early drug discovery, promoting biological relevance as a key selection criterion early in the drug development cascade. Graphical Abstract: Highlights: Molecular phenotyping stratifies compounds based on pathway profiles Molecular phenotyping detects false-positive hits in a phenotypic screen Molecular phenotyping correlates pathway activity patterns with phenotypic readouts Molecular phenotyping can be powered by preclinical and clinical data Abstract : Drawnel and Zhang et al. show that quantitative mRNA sequencing of pathway reporter genes can be powered by translational information and classifies compound responses. Adopting this technique in drug discovery could permit biomedically relevant compound screening, increasing likelihood of clinical impact. … (more)
- Is Part Of:
- Cell chemical biology. Volume 24:Issue 5(2017)
- Journal:
- Cell chemical biology
- Issue:
- Volume 24:Issue 5(2017)
- Issue Display:
- Volume 24, Issue 5 (2017)
- Year:
- 2017
- Volume:
- 24
- Issue:
- 5
- Issue Sort Value:
- 2017-0024-0005-0000
- Page Start:
- 624
- Page End:
- 634.e3
- Publication Date:
- 2017-05-18
- Subjects:
- molecular phenotypic screening -- high-throughput RNA sequencing -- pathway reporters -- drug discovery -- cardiomyocytes -- calcium signaling
Biochemistry -- Periodicals
572.05 - Journal URLs:
- http://www.cell.com/cell-chemical-biology/home ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.chembiol.2017.03.016 ↗
- Languages:
- English
- ISSNs:
- 2451-9456
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.733000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1838.xml