Serum Protein Expression Profiling for Cancer Detection: Validation of a SELDI-Based Approach for Prostate Cancer

Author:

Grizzle William E.1,Adam Bao-Ling2,Bigbee William L.3,Conrads Thomas P.4,Carroll Christopher5,Feng Ziding6,Izbicka Elzbieta7,Jendoubi Moncef8,Johnsey Donald9,Kagan Jacob9,Leach Robin J.5,McCarthy Diane B.10,Semmes O. John2,Srivastava Shiv11,Srivastava Sudhir9,Thompson Ian M.5,Thornquist Mark D.6,Verma Mukesh9,Zhang Zhen12,Zou Zhiqiang11

Affiliation:

1. University of Alabama at Birmingham, Birmingham, AL, USA

2. Eastern Virginia Medical School, Norfolk, VA, USA

3. University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA

4. SAIC-Frederick, Frederick, MD, USA

5. University of Texas Health Sciences Center San Antonio, San Antonio, TX, USA

6. Fred Hutchinson Cancer Research Center, Seattle, WA, USA

7. Institute of Drug Development, San Antonio Cancer Institute, San Antonio, TX, USA

8. Milagen, Inc., Richmond, CA, USA

9. National Cancer Institute, Rockville, MD, USA

10. Ciphergen Biosystems, Inc., Fremont, CA, USA

11. Uniformed Services University of Health Sciences, Rockville, MD, USA

12. Johns Hopkins Medical Institutions, Baltimore, MD, USA

Abstract

Multiple studies have reported that analysis of serum and other bodily fluids using surface enhanced laser desorption/ionization time of flight mass spectroscopy (SELDI-TOF-MS) can identify a “fingerprint” or “signature” of spectral peaks that can separate patients with a specific disease from normal control patients. Ultimately, classification by SELDI-TOF-MS relies on spectral differences in position and amplitude of resolved peaks. Since the reproducibility of quantitation, resolution and mass accuracy of the SELDI-TOF-MS, or any high throughput mass spectrometric technique, has never been determined this method has come under some skepticism as to its clinical usefulness. This manuscript describes a detailed design of a three-phase study to validate the clinical usefulness of SELDI-TOF-MS in the identification of patients with prostatic adenocarcinoma (PCA). At the end of this validation study, the usefulness of the general SELDI-TOF-MS approach to identifying patients with PCA will be demonstrated and how it compares with PCA diagnosis by measuring prostate specific antigen.

Funder

National Cancer Institute

Publisher

Hindawi Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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