Proteomics in prostate cancer biomarker discovery

Samantha Larkin(University of Portsmouth), Bashar Zeidan(University of Southampton), M. Taylor(University of Southampton), Bridget Bickers(University of Portsmouth), Jamal Alruwaili(University of Portsmouth), Claire Aukim-Hastie(University of Portsmouth), Paul A. Townsend(University of Southampton)
Expert Review of Proteomics
February 1, 2010
Cited by 22

Abstract

Despite advances in molecular medicine, genomics, proteomics and translational research, prostate cancer remains the second most common cause of cancer-related mortality for men in the Western world. Clearly, early detection, targeted treatment and post-treatment monitoring are vital tools to combat this disease. Tumor markers can be useful for diagnosis and early detection of cancer, assessment of prognosis, prediction of therapeutic effect and treatment monitoring. Such tumor markers include prostate-specific antigen (prostate), cancer antigen (CA)15.3 (breast), CA125 (ovarian), CA19.9 (gastrointestinal) and serum alpha-fetoprotein (testicular cancer). However, all of these biomarkers lack sensitivity and specificity and, therefore, there is a large drive towards proteomic biomarker discovery. Current research efforts are directed towards discovering biosignatures from biological samples using novel proteomic technologies that provide high-throughput, in-depth analysis and quantification of the proteome. Several of these studies have revealed promising biomarkers for use in diagnosis, assessment of prognosis, and targeting treatment of prostate cancer. This review focuses on prostate cancer proteomic biomarker discovery and its future potential.


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