Proteome Alterations in Primary Open Angle Glaucoma Aqueous Humor
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作者:
Izzotti, A.
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Univ Genoa, Fac Med, Dept Hlth Sci, I-16126 Genoa, ItalySt Martino Hosp, Ophthalmol Unit, Dept Head Neck Pathol, I-16132 Genoa, Italy
Izzotti, A.
[2
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Longobardi, M.
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Univ Genoa, Fac Med, Dept Hlth Sci, I-16126 Genoa, ItalySt Martino Hosp, Ophthalmol Unit, Dept Head Neck Pathol, I-16132 Genoa, Italy
Longobardi, M.
[2
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Cartiglia, C.
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Univ Genoa, Fac Med, Dept Hlth Sci, I-16126 Genoa, ItalySt Martino Hosp, Ophthalmol Unit, Dept Head Neck Pathol, I-16132 Genoa, Italy
Cartiglia, C.
[2
]
Sacca, S. C.
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St Martino Hosp, Ophthalmol Unit, Dept Head Neck Pathol, I-16132 Genoa, ItalySt Martino Hosp, Ophthalmol Unit, Dept Head Neck Pathol, I-16132 Genoa, Italy
Sacca, S. C.
[1
]
机构:
[1] St Martino Hosp, Ophthalmol Unit, Dept Head Neck Pathol, I-16132 Genoa, Italy
As the only nourishment and scavenging source for most of the anterior and posterior chamber tissues in the eye, the aqueous humor represents one of the target for glaucoma. The aim of this study is to investigate the yet unexplored relationship between aqueous humor protein content and open-angle glaucoma (POAG) pathogenesis. Aqueous humor was collected from 10 POAG patients (cases) and 14 senile cataract patients (controls), matched for age and gender, undergoing surgery for trabeculectomy and cataract, respectively. Protein samples were cyanine-labeled and hybridized with antibody microarrays. Microarray signals were revealed by laser scanner, quantified, and compared by statistical analyses. Total protein amounts were not significantly different in patients versus controls. Conversely, a proteome cluster significantly modified in patients as compared to controls was identified as highly predictive for disease status. Selected proteins underwent dramatic variation, which was correlated to pathogenetic events characterizing POAG, including oxidative damage, mitochondrial damage, neural degeneration, and apoptosis. The results obtained indicate that proteomic analysis of aqueous humor is a new tool for POAG diagnosis in the case of otherwise uncertain disease recognition. Furthermore, this study allows a better understanding of mechanisms involved in the pathogenesis of POAG, the main cause of irreversible blindness worldwide.
机构:
Mayo Clin, Dept Ophthalmol, Rochester, MN 55905 USAMayo Clin, Dept Ophthalmol, Rochester, MN 55905 USA
Howell, Kyle G.
Vrabel, Anne M.
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Mayo Clin, Dept Ophthalmol, Rochester, MN 55905 USAMayo Clin, Dept Ophthalmol, Rochester, MN 55905 USA
Vrabel, Anne M.
Chowdhury, Uttio Roy
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Mayo Clin, Dept Ophthalmol, Rochester, MN 55905 USAMayo Clin, Dept Ophthalmol, Rochester, MN 55905 USA
Chowdhury, Uttio Roy
Stamer, William Daniel
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机构:
Univ Arizona, Dept Ophthalmol & Vis Sci, Tucson, AZ USA
Univ Arizona, Dept Pharmacol, Tucson, AZ USAMayo Clin, Dept Ophthalmol, Rochester, MN 55905 USA
Stamer, William Daniel
Fautsch, Michael P.
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Mayo Clin, Dept Ophthalmol, Rochester, MN 55905 USAMayo Clin, Dept Ophthalmol, Rochester, MN 55905 USA
机构:
Duke Univ, Med Ctr, Dept Ophthalmol, Durham, NC 27705 USAMed Coll Georgia, Dept Cellular Biol & Anat, 1460 Laney Walker Blvd CB1101, Augusta, GA 30912 USA
Stamer, W. Daniel
Kuchtey, Rachel W.
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机构:
Vanderbilt Univ, Med Ctr, Vanderbilt Eye Inst, Nashville, TN 37232 USA
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USAMed Coll Georgia, Dept Cellular Biol & Anat, 1460 Laney Walker Blvd CB1101, Augusta, GA 30912 USA
Kuchtey, Rachel W.
Liu, Yutao
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机构:
Med Coll Georgia, Dept Cellular Biol & Anat, 1460 Laney Walker Blvd CB1101, Augusta, GA 30912 USA
Augusta Univ, James & Jean Culver Vis Discovery Inst, Augusta, GA 30912 USA
Augusta Univ, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAMed Coll Georgia, Dept Cellular Biol & Anat, 1460 Laney Walker Blvd CB1101, Augusta, GA 30912 USA