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Technical Briefs |
a author for correspondence: fax 619-536-8058, e-mail abblase@beckman.com
Prostate-specific antigen (PSA) has been established as a marker
to aid in detection and monitoring of prostate cancer
(1)(2). PSA in serum
exists predominantly in three forms: free, uncomplexed PSA; PSA
covalently complexed to
1-antichymotrypsin (PSA-ACT);
and PSA covalently complexed to
2-macroglobulin (PSA-MG)
(3). Immunoassays available today
recognize free PSA and PSA-ACT but not PSA-MG, and their result for
"total PSA" refers to the sum of the free and ACT-bound forms of
PSA as measured by the immunoassay.
In general, the proportion of free PSA relative to PSA-ACT is lower in prostate cancer patients than in normal subjects or in patients with noncancerous prostatic disease (4). The percentage of free PSA ranges from 5% to 50% when total serum PSA is 410 µg/L (5)(6). However, increased serum concentrations of PSA do not necessarily indicate prostate cancer because such values can also occur in cases of benign prostate hyperplasia or prostatitis (7)(8)(9).
Assays of total serum PSA differ from one another in an important respect: They do not recognize the free and ACT-bound species of PSA equivalently (10)(11). "Equimolar-response assays" measure equal molar concentrations of free PSA and PSA-ACT equivalently; "skewed-response assays" measure these PSA forms differently (12)(13)(14).
The total PSA concentration measured by an equimolar assay depends on
only the total concentration of free PSA plus PSA-ACT and is
independent of their relative proportions. The interpretation of
results reported by skewed-response assays, however, may be misleading
because (a) the proportion of free PSA is generally higher
in noncancer patients, and
Acknowledgments
Footnotes
References
The following articles in journals at HighWire Press have cited this article:
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S. A.R. Kort, F. Martens, H. Vanpoucke, H. L. van Duijnhoven, and M. A. Blankenstein Comparison of 6 Automated Assays for Total and Free Prostate-Specific Antigen with Special Reference to Their Reactivity toward the WHO 96/670 Reference Preparation Clin. Chem., August 1, 2006; 52(8): 1568 - 1574. [Abstract] [Full Text] [PDF] |
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A. Semjonow, F. Oberpenning, C. Weining, M. Schon, B. Brandt, G. De Angelis, A. Heinecke, M. Hamm, P. Stieber, L. Hertle, et al. Do Modifications of Nonequimolar Assays for Total Prostate-specific Antigen Improve Detection of Prostate Cancer? Clin. Chem., August 1, 2001; 47(8): 1472 - 1475. [Full Text] [PDF] |
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R. J. Laffin, D. W. Chan, M. J. Tanasijevic, G. A. Fischer, W. Markus, J. Miller, P. Matarrese, L. J. Sokoll, D. J. Bruzek, J. Eneman, et al. Hybritech Total and Free Prostate-specific Antigen Assays Developed for the Beckman Coulter Access Automated Chemiluminescent Immunoassay System: A Multicenter Evaluation of Analytical Performance Clin. Chem., January 1, 2001; 47(1): 129 - 132. [Full Text] [PDF] |
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M. P. Fox, A. A. Reilly, and E. Schneider Effect of the Ratio of Free to Total Prostate-specific Antigen on Interassay Variability in Proficiency Test Samples Clin. Chem., August 1, 1999; 45(8): 1181 - 1189. [Abstract] [Full Text] [PDF] |
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H. Nagasaki, M. Watanabe, N. Komatsu, T. Kaneko, J. Y. Dube, T. Kajita, Y. Saitoh, and Y. Ohta Epitope Analysis of a Prostate-specific Antigen (PSA) C-Terminal-specific Monoclonal Antibody and New Aspects for the Discrepancy between Equimolar and Skewed PSA Assays Clin. Chem., April 1, 1999; 45(4): 486 - 496. [Abstract] [Full Text] [PDF] |
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C. D. Cheli, M. Marcus, J. Levine, Z. Zhou, P. H. Anderson, D. D. Bankson, J. Bock, S. Bodin, C. Eisen, M. Senior, et al. Variation in the Quantitation of Prostate-specific Antigen in Reference Material: Differences in Commercial Immunoassays, Clin. Chem., July 1, 1998; 44(7): 1551 - 1553. [Full Text] [PDF] |
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P. C. Tewari, J. S. Williams, A. B. Blase, and R. L. Sokoloff Analytical Characteristics of Seminal Fluid PSA Differ from Those of Serum PSA Clin. Chem., January 1, 1998; 44(1): 191 - 193. [Full Text] [PDF] |
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