» Articles » PMID: 19305628

Proteomics: Analysis of Spectral Data

Overview
Journal Cancer Inform
Publisher Sage Publications
Date 2009 Mar 24
PMID 19305628
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

The goal of disease-related proteogenomic research is a complete description of the unfolding of the disease process from its origin to its cure. With a properly selected patient cohort and correctly collected, processed, analyzed data, large scale proteomic spectra may be able to provide much of the information necessary for achieving this goal. Protein spectra, which are one way of representing protein expression, can be extremely useful clinically since they can be generated from blood rather than from diseased tissue. At the same time, the analysis of circulating proteins in blood presents unique challenges because of their heterogeneity, blood contains a large number of different abundance proteins generated by tissues throughout the body. Another challenge is that protein spectra are massively parallel information. One can choose to perform top-down analysis, where the entire spectra is examined and candidate peaks are selected for further assessment. Or one can choose a bottom-up analysis, where, via hypothesis testing, individual proteins are identified in the spectra and related to the disease process. Each approach has advantages and disadvantages that must be understood if protein spectral data are to be properly analyzed. With either approach, several levels of information must be integrated into a predictive model. This model will allow us to detect disease and it will allow us to discover therapeutic interventions that reduce the risk of disease in at-risk individuals and effectively treat newly diagnosed disease.

Citing Articles

Revisiting the myths of protein interior: studying proteins with mass-fractal hydrophobicity-fractal and polarizability-fractal dimensions.

Banerji A, Ghosh I PLoS One. 2009; 4(10):e7361.

PMID: 19834622 PMC: 2760208. DOI: 10.1371/journal.pone.0007361.


Design of early validation trials of biomarkers.

Normolle D, Ruffin M, Brenner D Cancer Inform. 2009; 1:25-31.

PMID: 19305629 PMC: 2657653.


In vivo selection of phage for the optical imaging of PC-3 human prostate carcinoma in mice.

Newton J, Kelly K, Mahmood U, Weissleder R, Deutscher S Neoplasia. 2006; 8(9):772-80.

PMID: 16984734 PMC: 1584300. DOI: 10.1593/neo.06331.

References
1.
Catherino W, Prupas C, Tsibris J, Leppert P, Payson M, Nieman L . Strategy for elucidating differentially expressed genes in leiomyomata identified by microarray technology. Fertil Steril. 2003; 80(2):282-90. DOI: 10.1016/s0015-0282(03)00953-1. View

2.
Burke H . Discovering patterns in microarray data. Mol Diagn. 2001; 5(4):349-57. DOI: 10.1007/BF03262096. View

3.
Valk P, Verhaak R, Beijen M, Erpelinck C, Barjesteh van Waalwijk van Doorn-Khosrovani S, Boer J . Prognostically useful gene-expression profiles in acute myeloid leukemia. N Engl J Med. 2004; 350(16):1617-28. DOI: 10.1056/NEJMoa040465. View

4.
Perou C, Jeffrey S, van de Rijn M, Rees C, Eisen M, Ross D . Distinctive gene expression patterns in human mammary epithelial cells and breast cancers. Proc Natl Acad Sci U S A. 1999; 96(16):9212-7. PMC: 17759. DOI: 10.1073/pnas.96.16.9212. View

5.
Bostwick D, Burke H . Prediction of individual patient outcome in cancer: comparison of artificial neural networks and Kaplan--Meier methods. Cancer. 2001; 91(8 Suppl):1643-6. DOI: 10.1002/1097-0142(20010415)91:8+<1643::aid-cncr1177>3.0.co;2-i. View