|
|
||||||||||
|
J Am Coll Cardiol, 2006; 48:1733-1741, doi:10.1016/j.jacc.2006.06.063
(Published online 16 October 2006). © 2006 by the American College of Cardiology Foundation |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||

,


* Heart and Stroke/Richard Lewar Center of Excellence, University of Toronto and the Canadian Institutes of Health Research, Ottawa, Ontario, Canada
Department of Physiology
Banting and Best Department of Medical Research
Program in Proteomics and Bioinformatics, University of Toronto, Toronto, Ontario, Canada
|| Queen's University, Kingston, Ontario, Canada
¶ Department of Medicine, University of Toronto, Toronto, Ontario, Canada
# University of California Los AngelesDavid Geffen School of Medicine, Los Angeles, California
** Johns Hopkins NHLBI Proteomics Center, Baltimore, Maryland
Manuscript received February 9, 2006; revised manuscript received May 30, 2006, accepted June 5, 2006.
* Reprint requests and correspondence: Dr. Peter Liu, Heart & Stroke/Richard Lewar Centre of Excellence and Institute of Circulatory and Respiratory Health, Canadian Institute of Health Research, NCSB 11-1266, Toronto General Hospital, 200 Elizabeth Street, Toronto, Ontario M5G 2C4, Canada. (Email: peter.liu{at}utoronto.ca).
Proteomics is the new systems biological approach to the study of proteins and protein variation on a large scale as a result of biological processes and perturbations. The field is undergoing a dramatic transformation, owing to the completion and annotation of the human genome as well as technological advances to study proteins on a large scale. The new science of proteomics can potentially yield novel biomarkers reflecting cardiovascular disease, establish earlier detection strategies, and monitor responses to therapy. Technological advances permit the unprecedented large-scale identification of peptide sequences in a biological sample with mass spectrometry, whereas gel-based techniques provide further refinement on the status of post-translational modification. The application of high throughput protein evaluation with a subset of predefined targets, identified through proteomics, microarray profiling, and pathway analysis in animal models and human tissues, is gaining momentum in research and clinical applications. Proteomic analysis has provided important insights into ischemic heart disease, heart failure, and cardiovascular pathophysiology. The combination of proteomic biomarkers with clinical phenotypes and genetic haplotype information can lead to a more precise diagnosis and therapy on an individual basisthe fundamental premise of "personalized medicine."
| |||||
This article has been cited by other articles:
![]() |
E. Braunwald Biomarkers in Heart Failure N. Engl. J. Med., May 15, 2008; 358(20): 2148 - 2159. [Full Text] [PDF] |
||||
![]() |
P. Matt, Z. Fu, Q. Fu, and J. E. Van Eyk Biomarker discovery: proteome fractionation and separation in biological samples Physiol Genomics, March 10, 2008; 33(1): 12 - 17. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Stern Are We Getting Nearer to Screening for Atherosclerosis? Circulation, January 1, 2008; 117(1): 122 - 126. [Full Text] [PDF] |
||||
![]() |
A. N. DeMaria, O. Ben-Yehuda, G. K. Feld, G. S. Ginsburg, B. H. Greenberg, W. Y.W. Lew, J. A.C. Lima, A. S. Maisel, J. Narula, D. J. Sahn, et al. Highlights of the Year in JACC 2006 J. Am. Coll. Cardiol., January 30, 2007; 49(4): 509 - 527. [Full Text] [PDF] |
||||
| HOME | SUBSCRIPTIONS | CURRENT ISSUE | PAST ISSUES | CARDIOSOURCE | SEARCH | HELP | FEEDBACK |