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Identification of Biomarkers and Signatures in Protein Data

Nordling, Torbjörn E. M. (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi,Stockholm Bioinformat Ctr, Sci Life Lab, S-17121 Solna, Sweden.;Natl Cheng Kung Univ, Dept Mech Engn, Tainan 70101, Taiwan.;Nordron AB, S-17065 Solna, Sweden.
Padhan, Narendra (författare)
Uppsala universitet,Vaskulärbiologi
Nelander, Sven (författare)
Uppsala universitet,Neuroonkologi
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Claesson-Welsh, Lena (författare)
Uppsala universitet,Vaskulärbiologi
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 (creator_code:org_t)
2015
2015
Engelska.
Ingår i: 2015 IEEE 11Th International Conference On E-Science. - 9781467393256 ; , s. 411-419
  • Konferensbidrag (refereegranskat)
Abstract Ämnesord
Stäng  
  • The correct diagnosis of cancer patients conventionally depends on the pathologist's experience and ability to distinguish cancer tissue from normal tissue under a microscope. Advances in technology for measuring the abundance of, e.g., proteins and mRNAs in tissue samples make it interesting to search for an optimal subset of these for classification of samples as cancer or normal. We discuss issues of identification of biomarkers that provide distinct signatures for prediction of tissues as cancer or normal, exemplified by our recent study of cancer signalling signatures in human colon cancer characterised with regards to protein abundance using high sensitivity isoelectric focusing. We show that the optimal subset for separation of cancer tissues from normal tissues does not contain any of the proteins in the top quintile in terms of significant difference between the groups according to Mann-Whitney U-test or correlation to the diagnosis. Actually, one of the proteins belongs to the tertile with the lowest significance and correlation. This highlights the weakness of the practice of only looking for significant differences in the abundance of individual proteins and raises the question of how many lifesaving discoveries that have been missed due to it. We also demonstrate how Monte Carlo simulations of the separation with random class assignment can be used to calculate p-values for observing any specific separation by chance and selection of the optimal number of proteins in the subset based on these p-values. Both selection of the optimal number of biomarkers and calculation of p-values corrected for multiple hypothesis testing are essential to obtain a subset of biomarkers that yield robust predictions for clinical use.

Ämnesord

NATURVETENSKAP  -- Data- och informationsvetenskap (hsv//swe)
NATURAL SCIENCES  -- Computer and Information Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Biomarkers
Mann-Whitney U test
Student's t-test
Spearman's rank correlation
Subset selection
Variable selection
Feature selection
Monte Carlo simulations
p-values
Cancer
Colon cancer
Protein abundance

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