P504S - A new molecular marker for the detection of prostate carcinoma

被引:313
作者
Jiang, Z
Woda, BA
Rock, KL
Xu, YD
Savas, L
Khan, A
Pihan, G
Cai, F
Babcook, JS
Rathanaswami, P
Reed, SG
Xu, JC
Fanger, GR
机构
[1] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01655 USA
[2] Corixa Corp, Seattle, WA USA
[3] Abgenix Biopharma Inc, Vancouver, BC, Canada
关键词
prostate carcinoma; P504S; immunocytochemistry;
D O I
10.1097/00000478-200111000-00007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The ability to diagnose prostate carcinoma would be improved by the detection of a tumor-associated antigen. P504S, a cytoplasmic protein, was recently identified by cDNA library subtraction in conjunction with high throughput microarray screening from prostate carcinoma. The aim of this study was to establish the pattern of expression of P504S in prostate carcinoma and benign prostatic tissue. A total of 207 cases, including, 137 cases of prostate carcinoma and 70 cases of benign prostate, from prostatectomies (n = 77), prostate needle biopsies (n = 112), and transurethral prostate resections (n = 18) were examined by immunocytochemistry for P504S. P504S showed strong cytoplasmic granular staining in 100% of prostate carcinomas regardless of Gleason scores and diffuse (> 75% of tumor) staining in 92% of cases. In contrast, 171 of 194 (88%) of benign prostates, including 56 of 67 (84%) benign prostate cases and 115 of 127 (91%) cases of benign,glands adjacent to cancers were negative for P504S. The remainders of benign prostates were focally and weakly positive for P504S. The staining pattern of these normal glands was different and easily distinguishable from that observed in prostate carcinoma. Expression of P504S was not found in basal cell hyperplasia, urothelial cells/metaplasia and small atrophic glands that may mimic prostate carcinoma. Our findings indicate that P504S is a highly sensitive and specific positive marker for prostate carcinoma.
引用
收藏
页码:1397 / 1404
页数:8
相关论文
共 25 条
[1]   A novel strategy for generating monoclonal antibodies from single, isolated lymphocytes producing antibodies of defined specificities [J].
Babcook, JS ;
Leslie, KB ;
Olsen, OA ;
Salmon, RA ;
Schrader, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7843-7848
[2]  
BECKETT ML, 1991, CANCER RES, V51, P1326
[3]  
BRAWER MK, 1985, CANCER RES, V45, P3663
[4]   Increasing incidence of minimal residual cancer in radical prostatectomy specimens [J].
DiGiuseppe, JA ;
Sauvageot, J ;
Epstein, JI .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (02) :174-178
[5]  
EDWARDS JJ, 1982, CLIN CHEM, V28, P160
[6]   PATHOLOGICAL AND CLINICAL FINDINGS TO PREDICT TUMOR EXTENT OF NONPALPABLE (STAGE-T1C) PROSTATE-CANCER [J].
EPSTEIN, JI ;
WALSH, PC ;
CARMICHAEL, M ;
BRENDLER, CB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (05) :368-374
[7]  
Ferdinandusse S, 2000, J LIPID RES, V41, P1890
[8]  
Gaudin P B, 1997, Anat Pathol, V2, P111
[9]  
GOWN AM, 1984, AM J PATHOL, V114, P309
[10]   AN EVALUATION OF PROSTATE SPECIFIC ANTIGEN IN PROSTATIC-CANCER [J].
GUINAN, P ;
BHATTI, R ;
RAY, P .
JOURNAL OF UROLOGY, 1987, 137 (04) :686-689