Benign prostate-specific antigen (BPSA) in serum is increased in benign prostate disease

被引:81
作者
Linton, HJ
Marks, LS
Millar, LS
Knott, CL
Rittenhouse, HG
Mikolajczyk, SD
机构
[1] Hybritech Inc, San Diego, CA 92121 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Urol Surg, Los Angeles, CA 90095 USA
关键词
D O I
10.1373/49.2.253
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: BPSA is a "benign" form of free prostate-specific antigen (PSA) that is increased in prostate transition zone tissues of men with pathologic benign prostatic hyperplasia (BPH). We developed an immunoassay to determine the concentration of BPSA in the serum of men with BPH. Methods: The BPSA antigen was purified by HPLC, and murine monoclonal antibodies were prepared by standard methods. A fluorogenic ELISA was developed with high specificity for BPSA and no cross-reactivity with other forms of PSA. Results: The BPSA immunoassay had a lower limit of detection of 6 ng/L and a cross-reactivity of <1% with all other clipped and nonclipped forms of PSA. The BPSA antibody was specific for the internal Lys(182) cleavage site that characterizes BPSA. Biopsy-negative men with a median total PSA of 4.8 mug/L had a median of 0.22 mug/L BPSA, representing 25% of the free PSA in serum. BPSA ranged from 0% to 60% of the free PSA in serum. BPSA in a cohort of cancer serum also comprised 25% of the free PSA. Control serum from women or men without increased PSA had nondetectable BPSA. Conclusions: BPSA is a significant percentage of the free PSA in BPH serum but not in control serum. The presence of prostate cancer does not alter the relative proportions of BPSA in sera with <10 mug/L PSA. BPSA has a wide distribution of concentrations in the serum and may provide clinical information for the study of men with BPH. (C) 2003 American Association for Clinical Chemistry.
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页码:253 / 259
页数:7
相关论文
共 27 条
[1]   The role of molecular forms of prostate-specific antigen (PSA or hK3) and of human glandular kallikrein 2 (hK2) in the diagnosis and monitoring of prostate cancer and in extra-prostatic disease [J].
Becker, C ;
Noldus, J ;
Diamandis, E ;
Lilja, H .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2001, 38 (05) :357-399
[2]   MEASUREMENT OF PROSTATE-SPECIFIC ANTIGEN IN SERUM AS A SCREENING-TEST FOR PROSTATE-CANCER [J].
CATALONA, WJ ;
SMITH, DS ;
RATLIFF, TL ;
DODDS, KM ;
COPLEN, DE ;
YUAN, JJJ ;
PETROS, JA ;
ANDRIOLE, GL .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (17) :1156-1161
[3]   Use of the percentage of free prostate-specific antigen to enhance differentiation of prostate cancer from benign prostatic disease - A prospective multicenter clinical trial [J].
Catalona, WJ ;
Partin, AW ;
Slawin, KM ;
Brawer, MK ;
Flanigan, RC ;
Patel, A ;
Richie, JP ;
deKernion, JB ;
Walsh, PC ;
Scardino, PT ;
Lange, PH ;
Subong, ENP ;
Parson, RE ;
Gasior, GH ;
Loveland, KG ;
Southwick, PC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (19) :1542-1547
[4]   Polyclonal and monoclonal antibodies to prostate-specific antigen can cross-react with human kallikrein 2 and human kallikrein 1 [J].
Finlay, JA ;
Day, JR ;
Rittenhouse, HG .
UROLOGY, 1999, 53 (04) :746-751
[5]   Molecular heterogeneity of free PSA in sera of patients with benign and malignant prostate tumors [J].
Hilz, H ;
Noldus, J ;
Hammerer, P ;
Buck, F ;
Lück, M ;
Huland, H .
EUROPEAN UROLOGY, 1999, 36 (04) :286-292
[6]  
KNOTT CL, 1997, PRINCIPLES PRACTICE, P37
[7]  
Kumar A, 2000, PROSTATE, V44, P248, DOI 10.1002/1097-0045(20000801)44:3<248::AID-PROS10>3.0.CO
[8]  
2-D
[9]  
Kumar A, 1997, CANCER RES, V57, P3111
[10]   SERUM PROSTATE SPECIFIC ANTIGEN AS PRE-SCREENING TEST FOR PROSTATE-CANCER [J].
LABRIE, F ;
DUPONT, A ;
SUBURU, R ;
CUSAN, L ;
TREMBLAY, M ;
GOMEZ, JL ;
EMOND, J ;
STAMEY, TA ;
LANGE, PH .
JOURNAL OF UROLOGY, 1992, 147 (03) :846-852