Literature DB >> 27121749

Cancer associated proteins in blood plasma: Determining normal variation.

Markus Stenemo1,2, Johan Teleman1, Martin Sjöström2, Gabriel Grubb2, Erik Malmström1, Johan Malmström1, Emma Niméus2,3.   

Abstract

Protein biomarkers have the potential to improve diagnosis, stratification of patients into treatment cohorts, follow disease progression and treatment response. One distinct group of potential biomarkers comprises proteins which have been linked to cancer, known as cancer associated proteins (CAPs). We determined the normal variation of 86 CAPs in 72 individual plasma samples collected from ten individuals using SRM mass spectrometry. Samples were collected weekly during 5 weeks from ten volunteers and over one day at nine fixed time points from three volunteers. We determined the degree of the normal variation depending on interpersonal variation, variation due to time of day, and variation over weeks and observed that the variation dependent on the time of day appeared to be the most important. Subdivision of the proteins resulted in two predominant protein groups containing 21 proteins with relatively high variation in all three factors (day, week and individual), and 22 proteins with relatively low variation in all factors. We present a strategy for prioritizing biomarker candidates for future studies based on stratification over their normal variation and have made all data publicly available. Our findings can be used to improve selection of biomarker candidates in future studies and to determine which proteins are most suitable depending on study design.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Biomarkers; Biomedicine; Blood proteome; Cancer associated proteins; Mass spectrometry; Normal variation

Mesh:

Substances:

Year:  2016        PMID: 27121749     DOI: 10.1002/pmic.201500204

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  4 in total

1.  Internal Standard Triggered-Parallel Reaction Monitoring Mass Spectrometry Enables Multiplexed Quantification of Candidate Biomarkers in Plasma.

Authors:  Jacob J Kennedy; Jeffrey R Whiteaker; Richard G Ivey; Aura Burian; Shrabanti Chowdhury; Chia-Feng Tsai; Tao Liu; ChenWei Lin; Oscar D Murillo; Rachel A Lundeen; Lisa A Jones; Philip R Gafken; Gary Longton; Karin D Rodland; Steven J Skates; John Landua; Pei Wang; Michael T Lewis; Amanda G Paulovich
Journal:  Anal Chem       Date:  2022-06-29       Impact factor: 8.008

2.  Plasma Protein Timings: Relative Contributions of Storage Time, Donor Age and Donation Season.

Authors:  Jose A Cancelas; Neeta Rugg
Journal:  EBioMedicine       Date:  2016-10-05       Impact factor: 8.143

3.  Effects of Long-Term Storage Time and Original Sampling Month on Biobank Plasma Protein Concentrations.

Authors:  Stefan Enroth; Göran Hallmans; Kjell Grankvist; Ulf Gyllensten
Journal:  EBioMedicine       Date:  2016-08-26       Impact factor: 8.143

4.  Streptococcus pyogenes Infection and the Human Proteome with a Special Focus on the Immunoglobulin G-cleaving Enzyme IdeS.

Authors:  Christofer A Q Karlsson; Sofia Järnum; Lena Winstedt; Christian Kjellman; Lars Björck; Adam Linder; Johan A Malmström
Journal:  Mol Cell Proteomics       Date:  2018-03-06       Impact factor: 5.911

  4 in total

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