Urinary Proteomics and Drug Discovery in Chronic Kidney Disease: A New Perspective

被引:10
|
作者
Prunotto, Marco [1 ]
Ghiggeri, Gian Marco [2 ]
Candiano, Giovanni [2 ]
Lescuyer, Pierre [3 ]
Hochstrasser, Denis [3 ]
Moll, Solange
机构
[1] Hoffmann La Roche Ltd, Pharma Res Dev & Metab Dis, Basel, Switzerland
[2] Giannina Gaslini Childrens Hosp, Nephrol Unit Lab, Genoa, Italy
[3] Geneva Univ Hosp, Clin Prote Lab, Dept Genet & Lab Med, Geneva, Switzerland
关键词
CKD; biomarker; drug discovery; urine; proteomics; ENDOPLASMIC-RETICULUM STRESS; PROXIMAL TUBULAR CELLS; MASS-SPECTROMETRY; CAPILLARY-ELECTROPHORESIS; DIABETIC-NEPHROPATHY; BIOMARKER DISCOVERY; CLINICAL PROTEOMICS; DIAGNOSTIC PURPOSES; LUPUS-ERYTHEMATOSUS; LIGAND LIBRARIES;
D O I
10.1021/pr100464q
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chronic kidney disease (CKD) is becoming a worldwide public health problem. The identification of a specific set of early biomarkers for CKD is extremely relevant to progress in disease knowledge, improving diagnosis, treatment, or development, and monitoring efficacy of new drugs. As kidney fibrosis can be considered the common pathological way to end stage renal failure, independent of the initial renal insult, these biomarkers are therefore biomarkers of early tubulo-interstitial fibrosis. The availability of a specific set of biomarkers for CKD is the mandatory condition to create new dedicated drugs and validate them in clinics without waiting years for a functional response in patients. We suggest here specific cohorts of patients where this early signature of fibrosis may be simpler to be identified.
引用
收藏
页码:126 / 132
页数:7
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