Skip to content Skip to navigation

Personalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal Disease.

TitlePersonalized Proteomics for Precision Health: Identifying Biomarkers of Vitreoretinal Disease.
Publication TypeJournal Article
Year of Publication2018
AuthorsVelez, Gabriel, Tang Peter H., Cabral Thiago, Cho Galaxy Y., Machlab Daniel A., Tsang Stephen H., Bassuk Alexander G., and Mahajan Vinit B.
JournalTransl Vis Sci Technol
Volume7
Issue5
Pagination12
Date Published2018 Sep
ISSN2164-2591
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.

Translational Relevance: 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.

DOI10.1167/tvst.7.5.12
Alternate JournalTransl Vis Sci Technol
PubMed ID30271679
PubMed Central IDPMC6159735
Grant ListR21 AG050437 / AG / NIA NIH HHS / United States
R01 EY018213 / EY / NEI NIH HHS / United States
R01 EY024665 / EY / NEI NIH HHS / United States
R01 EY026682 / EY / NEI NIH HHS / United States
R01 EY024698 / EY / NEI NIH HHS / United States
P30 EY019007 / EY / NEI NIH HHS / United States
R01 EY025225 / EY / NEI NIH HHS / United States
P30 CA013696 / CA / NCI NIH HHS / United States
T32 GM007337 / GM / NIGMS NIH HHS / United States