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Proteomics for the identification of new prostate cancer biomarkers.

Publication ,  Journal Article
Ornstein, DK; Tyson, DR
Published in: Urol Oncol
2006

Molecular profiling studies of human prostate cancer provide great opportunities to identify new prostate cancer biomarkers to improve prostate cancer detection and treatment. Proteomics has distinct advantages over genomic and ribonucleic acid expression studies because it is the proteins that are ultimately responsible for the malignant phenotype. The goal of traditional proteomic studies is to identify disease-specific biomarkers. Two-dimensional (2-D) gel electrophoresis (polyacrylamide gel electrophoresis; PAGE) coupled with mass spectrometry is the most widely used experimental strategy and, to date, has yielded several potentially relevant prostate cancer biomarkers. A promising prostate cancer biomarker identified by 2-D PAGE and mass spectrometry is annexin I. Studies have already confirmed that annexin I is underexpressed in a majority of early stage prostate cancers. Other non-gel-based proteomic technologies that may have improved sensitivity as compared to 2-D PAGE have recently been developed. An example of this is the ProteomeLab PF 2-D (Beckman Coulter, Inc., Fullerton, CA). The goal of most proteomic studies is to identify biomarkers that can be measured by enzyme-linked immunosorbent assay or immunohistochemistry. Improvements in proteomic technology may be changing this paradigm because there are now efforts to develop proteomic technologies directly into clinical diagnostic tests. An example of this technology is surface-enhanced laser desorption ionization time-of-flight mass spectrometry. Using this technology combined with a pattern recognition based bioinformatics tool, discriminatory spectrum proteomic profiles were generated that could help discriminate men with prostate cancer from those with benign prostates. If several technologic hurdles can be overcome, it is possible that methodology will improve the specificity and sensitivity of prostate cancer detection.

Duke Scholars

Published In

Urol Oncol

DOI

ISSN

1078-1439

Publication Date

2006

Volume

24

Issue

3

Start / End Page

231 / 236

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Proteomics
  • Prostatic Neoplasms
  • Neoplasm Proteins
  • Mass Spectrometry
  • Male
  • Humans
  • Electrophoresis, Gel, Two-Dimensional
  • Biomarkers, Tumor
  • 3211 Oncology and carcinogenesis
 

Citation

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ICMJE
MLA
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Ornstein, D. K., & Tyson, D. R. (2006). Proteomics for the identification of new prostate cancer biomarkers. Urol Oncol, 24(3), 231–236. https://doi.org/10.1016/j.urolonc.2005.11.035
Ornstein, David K., and Darren R. Tyson. “Proteomics for the identification of new prostate cancer biomarkers.Urol Oncol 24, no. 3 (2006): 231–36. https://doi.org/10.1016/j.urolonc.2005.11.035.
Ornstein DK, Tyson DR. Proteomics for the identification of new prostate cancer biomarkers. Urol Oncol. 2006;24(3):231–6.
Ornstein, David K., and Darren R. Tyson. “Proteomics for the identification of new prostate cancer biomarkers.Urol Oncol, vol. 24, no. 3, 2006, pp. 231–36. Pubmed, doi:10.1016/j.urolonc.2005.11.035.
Ornstein DK, Tyson DR. Proteomics for the identification of new prostate cancer biomarkers. Urol Oncol. 2006;24(3):231–236.
Journal cover image

Published In

Urol Oncol

DOI

ISSN

1078-1439

Publication Date

2006

Volume

24

Issue

3

Start / End Page

231 / 236

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Proteomics
  • Prostatic Neoplasms
  • Neoplasm Proteins
  • Mass Spectrometry
  • Male
  • Humans
  • Electrophoresis, Gel, Two-Dimensional
  • Biomarkers, Tumor
  • 3211 Oncology and carcinogenesis