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The Proteomics Big Challenge for Biomarkers and New Drug-Targets Discovery

Department of Health Sciences, Laboratory of Mass Spectrometry and Proteomics, University “Magna Græcia”, Catanzaro, University Campus, Europa Avenue, 88100 Catanzaro, Italy
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Int. J. Mol. Sci. 2012, 13(11), 13926-13948; https://doi.org/10.3390/ijms131113926
Received: 24 September 2012 / Revised: 17 October 2012 / Accepted: 25 October 2012 / Published: 29 October 2012
(This article belongs to the Collection Advances in Proteomic Research)
In the modern process of drug discovery, clinical, functional and chemical proteomics can converge and integrate synergies. Functional proteomics explores and elucidates the components of pathways and their interactions which, when deregulated, lead to a disease condition. This knowledge allows the design of strategies to target multiple pathways with combinations of pathway-specific drugs, which might increase chances of success and reduce the occurrence of drug resistance. Chemical proteomics, by analyzing the drug interactome, strongly contributes to accelerate the process of new druggable targets discovery. In the research area of clinical proteomics, proteome and peptidome mass spectrometry-profiling of human bodily fluid (plasma, serum, urine and so on), as well as of tissue and of cells, represents a promising tool for novel biomarker and eventually new druggable targets discovery. In the present review we provide a survey of current strategies of functional, chemical and clinical proteomics. Major issues will be presented for proteomic technologies used for the discovery of biomarkers for early disease diagnosis and identification of new drug targets. View Full-Text
Keywords: biomarkers; mass spectrometry; MALDI-TOF; proteomics; bodily fluids; tissues biomarkers; mass spectrometry; MALDI-TOF; proteomics; bodily fluids; tissues
MDPI and ACS Style

Savino, R.; Paduano, S.; Preianò, M.; Terracciano, R. The Proteomics Big Challenge for Biomarkers and New Drug-Targets Discovery. Int. J. Mol. Sci. 2012, 13, 13926-13948.

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