| Literature DB >> 24713096 |
Carol E Parker1, Christoph H Borchers2.
Abstract
In its early years, mass spectrometry (MS)-based proteomics focused on the cataloging of proteins found in different species or different tissues. By 2005, proteomics was being used for protein quantitation, typically based on "proteotypic" peptides which act as surrogates for the parent proteins. Biomarker discovery is usually done by non-targeted "shotgun" proteomics, using relative quantitation methods to determine protein expression changes that correlate with disease (output given as "up-or-down regulation" or "fold-increases"). MS-based techniques can also perform "absolute" quantitation which is required for clinical applications (output given as protein concentrations). Here we describe the differences between these methods, factors that affect the precision and accuracy of the results, and some examples of recent studies using MS-based proteomics to verify cancer-related biomarkers.Entities:
Keywords: Biomarker discovery; Biomarkers; Cancer; Mass spectrometry; Multiple reaction monitoring; Plasma or serum; Selected reaction monitoring; Targeted proteomics; Validation; Verification
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Year: 2014 PMID: 24713096 PMCID: PMC5528535 DOI: 10.1016/j.molonc.2014.03.006
Source DB: PubMed Journal: Mol Oncol ISSN: 1574-7891 Impact factor: 6.603