Differential Percentage of Serum Prostate-Specific Antigen Subforms Suggests a New Way to Improve Prostate Cancer Diagnosis

被引:34
作者
Sarrats, Ariadna [1 ]
Comet, Josep [2 ]
Tabares, Gloria [3 ]
Ramirez, Manel [4 ]
Nuria Aleixandre, R. [4 ]
de Llorens, Rafael [1 ]
Peracaula, Rosa [1 ]
机构
[1] Univ Girona, Unitat Bioquim & Biol Mol, Dept Biol, Girona 17071, Spain
[2] Hosp Univ Dr Josep Trueta, Unitat Urol, Girona, Spain
[3] Roche Diagnost, Dept Prot Chem, Penzberg, Germany
[4] Hosp Univ Dr Josep Trueto, Lab ICS Girona, Girona, Spain
关键词
benign prostatic hyperplasia; prostate cancer; prostate-specific antigen; sialic acid; two-dimensional electrophoresis; ALTERED GLYCOSYLATION; FREE PSA; COMPLEX; ALPHA-1-ANTICHYMOTRYPSIN; ELECTROPHORESIS; HYPERPLASIA; FORMS; MEN;
D O I
10.1002/pros.21031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Prostate-specific antigen (PSA) is the tumor marker Currently used for Prostate cancer (PCa) screening and diagnosis. However, its use is controversial as serum PSA levels are also increased in other non-malignant prostatic diseases such as benign prostatic hyperplasia (BPH). PSA sialic acid content is altered in tumor situation and modifies PSA's isoelectric point (p/). Our goal has been to evaluate serum PSA subforms from PCa and BPH patients by two-dimensional electrophoresis (2-DE) and to investigate whether they could be used to improve PCa diagnosis. METHODS. PSA from 20 PCa and 20 BPH patients' sera was subjected to a four-step method to obtain serum PSA 2-DE subforms from free PSA (fPSA) plus PSA released from the complex with alpha-1-antichymotrypsin. Relative percentages of PSA spots were quantified and subjected to statistical analysis. RESULTS. Five PSA subforms (F1, F2, F3, F4, and F5) of different p/ were obtained. Relative percentages of F3 (%F3) and F4 (%F4) were different between PCa and BPH groups. %F3 decreased in cancers and this decrease correlated with the cancer stage, while F4 behaved oppositely. These observations were also found when only focusing on the patients within the low total PSA (tPSA) range 2-20 ng/ml. CONCLUSIONS. %F3 showed a tendency. of higher sensitivity and specificity than the currently used tPSA and %fPSA tests. Therefore, %F3 measurement should be investigated in a larger cohort of patients to study whether it could be introduced to improve PCa diagnosis. Prostate 70: 1-9, 2010. (c) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 35 条
[1]   Biology of prostate-specific antigen [J].
Balk, SP ;
Ko, YJ ;
Bubley, GJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (02) :383-391
[2]   Characterization of epitope structure for 53 monoclonal antibodies against prostate-specific antigen [J].
Becker, C ;
Wigheden, I ;
Lilja, H .
TUMOR BIOLOGY, 1999, 20 :13-17
[3]   Cancer of the prostate [J].
Bracarda, S ;
de Cobelli, O ;
Greco, C ;
Prayer-Galetti, T ;
Valdagni, R ;
Gatta, G ;
de Braud, F ;
Bartsch, G .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2005, 56 (03) :379-396
[4]   Measurement of complexed PSA improves specificity for early detection of prostate cancer [J].
Brawer, MK ;
Meyer, GE ;
Letran, JL ;
Bankson, DD ;
Morris, DL ;
Yeung, KK ;
Allard, WJ .
UROLOGY, 1998, 52 (03) :372-378
[5]   Comparison of percent free PSA, PSA density, and age-specific PSA cutoffs for prostate cancer detection and staging [J].
Catalona, WJ ;
Southwick, PC ;
Slawin, KM ;
Partin, AW ;
Brawer, MK ;
Flanigan, RC ;
Patel, A ;
Richie, JP ;
Walsh, PC ;
Scardino, PT ;
Lange, PH ;
Gasior, GH ;
Loveland, KG ;
Bray, KR .
UROLOGY, 2000, 56 (02) :255-260
[6]   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
[7]  
Charrier JP, 1999, ELECTROPHORESIS, V20, P1075, DOI 10.1002/(SICI)1522-2683(19990101)20:4/5<1075::AID-ELPS1075>3.0.CO
[8]  
2-K
[9]   Prostate cancer [J].
Damber, Jan-Erik ;
Aus, Gunnar .
LANCET, 2008, 371 (9625) :1710-1721
[10]   Should the Gleason grading system for prostate cancer be modified to account for high-grade tertiary components? A systematic review and meta-analysis [J].
Harnden, Patricia ;
Shelley, Mike D. ;
Coles, Bernadette ;
Staffurth, John ;
Mason, Malcom D. .
LANCET ONCOLOGY, 2007, 8 (05) :411-419