Identification of Phosphoproteins and their Impact as Biomarkers in Cancer Therapeutics

Author(s): Samantha M. Frawley Cass, Jetze J. Tepe

Journal Name: Current Signal Transduction Therapy

Volume 6 , Issue 1 , 2011

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Abstract:

Many cellular processes are regulated by the reversible reaction of protein phosphorylation on serine, threonine and tyrosine residues. Deregulation of the signal transduction cascade upsets this well-balanced system and has been implicated in many diseases, including cancer. Identification of the proteins and post-translational modifications (PTMs) involved in the breakdown of certain cell signaling pathways provide unique insight into the diseases pathology. The importance of phosphorylation on a molecular level has been implicated specifically within signaling pathways involved in the pathogenesis of cancer. Emerging phosphoproteomic technologies have proven to be valuable tools in identifying new biomarkers, which presents an opportunity to probe phosphoproteins in specific cancer related pathways for both diagnosis and therapeutic exploitation. This review will discuss the development and impact of current phosphoproteomic identification and quantification methodologies and the utility of these technologies to assist in the determination of phosphoproteins as potential biomarkers and/or drug targets in cancer.

Keywords: Phosphorylation, phosphoprotein enrichment, cancer biomarkers, PTM, pI, IEF, SCX, SAX, HPLC, LC-MS, 2DE, CID, MALDI-MS, ESI-MS, MS/MS, ETD, ECD, IMAC, DA, NTA, ICAT, SILAC, PF2D, HCC, EGF, EGFR, SIMAC, NF-B, IKK, TNF, glutamic/aspartic acid residues, type II diabetes, Alzheimer's disease, mass spectrometry (MS) technologies, strong anion/cation exchange chromatography (SAX and SCX), iron, gallium, metal oxides, titanium dioxide, zirconium dioxide, phos-phoproteomic analysis, 32P Radiolabeling, Gel electrophoresis/Phosphoprotein Staining, Phosphospecific Antibodies, PHOSPHOPROTEOMIC ENRICHMENT-MASS SPECTROMETRY TECHNIQUES, IMAC-Immobilized Metal Affinity Chromatography, Strong Ion Exchange Chromatography, dihydroxybenzoic acid (DHB), MALDI MS, biotin affinity chromatography

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Article Details

VOLUME: 6
ISSUE: 1
Year: 2011
Page: [113 - 140]
Pages: 28
DOI: 10.2174/157436211794109389

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