Article ID Journal Published Year Pages File Type
1965568 Clinica Chimica Acta 2013 5 Pages PDF
Abstract

BackgroundFor many diseases such as cancer where phosphorylation-dependent signaling is the foundation of disease onset and progression, single-gene testing and genomic profiling alone are not sufficient in providing most critical information. The reason for this is that in these activated pathways the signaling changes and drug resistance are often not directly correlated with changes in protein expression levels. In order to obtain the essential information needed to evaluate pathway activation or the effects of certain drugs and therapies on the molecular level, the analysis of changes in protein phosphorylation is critical.MethodsExisting approaches do not differentiate clinical disease subtypes on the protein and signaling pathway level, and therefore hamper the predictive management of the disease and the selection of therapeutic targets.ConclusionsThe mini-review examines the impact of emerging systems biology tools and the possibility of applying phosphoproteomics to clinical research.

► Personalized medicine redefines current and future clinical research. ► Phosphoproteomics measures signaling pathways for better description of cellular states. ► Current phosphoproteomics platforms are not appropriate for clinical research. ► A new platform embracing protein arrays and targeted proteomics is proposed for clinical research.

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Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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