Journal article
Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal Disease
Translational vision science & technology, Vol.7(5), pp.12-12
09/2018
DOI: 10.1167/tvst.7.5.12
PMCID: PMC6159735
PMID: 30271679
Abstract
Proteomic analysis is an attractive and powerful tool for characterizing the molecular profiles of diseased tissues, such as the vitreous. The complexity of data available for analysis ranges from single (e.g., enzyme-linked immunosorbent assay [ELISA]) to thousands (e.g., mass spectrometry) of proteins, and unlike genomic analysis, which is limited to denoting risk, proteomic methods take snapshots of a diseased vitreous to evaluate ongoing molecular processes in real time. The proteome of diseased ocular tissues was recently characterized, uncovering numerous biomarkers for vitreoretinal diseases and identifying protein targets for approved drugs, allowing for drug repositioning. These biomarkers merit more attention regarding their therapeutic potential and prospective validation, as well as their value as reproducible, sensitive, and specific diagnostic markers.
Personalized proteomics offers many advantages over alternative precision-health platforms for the diagnosis and treatment of vitreoretinal diseases, including identification of molecular constituents in the diseased tissue that can be targeted by available drugs.
Details
- Title: Subtitle
- Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal Disease
- Creators
- Gabriel Velez - Medical Scientist Training Program, University of Iowa, Iowa City, IA, USAPeter H Tang - Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, USAThiago Cabral - Department of Ophthalmology, Federal University of São Paulo (UNIFESP), São Paulo, BrazilGalaxy Y Cho - Department of Ophthalmology, Columbia University, New York, NY, USADaniel A Machlab - Department of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USAStephen H Tsang - Department of Pathology & Cell Biology, College of Physicians & Surgeons, Columbia University, New York, NY, USAAlexander G Bassuk - Department of Pediatrics, University of Iowa, Iowa City, IA, USAVinit B Mahajan - Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, USA
- Resource Type
- Journal article
- Publication Details
- Translational vision science & technology, Vol.7(5), pp.12-12
- DOI
- 10.1167/tvst.7.5.12
- PMID
- 30271679
- PMCID
- PMC6159735
- NLM abbreviation
- Transl Vis Sci Technol
- ISSN
- 2164-2591
- eISSN
- 2164-2591
- Publisher
- United States
- Grant note
- R01 EY025225 / NEI NIH HHS R01 EY018213 / NEI NIH HHS P30 CA013696 / NCI NIH HHS T32 GM007337 / NIGMS NIH HHS R01 EY024698 / NEI NIH HHS R01 EY026682 / NEI NIH HHS R01 EY024665 / NEI NIH HHS R21 AG050437 / NIA NIH HHS P30 EY019007 / NEI NIH HHS
- Language
- English
- Date published
- 09/2018
- Academic Unit
- Neurology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Neurology (Pediatrics)
- Record Identifier
- 9984070530602771
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