Utility of immunohistochemical detection of prostate-specific Ets for the diagnosis of benign and malignant prostatic epithelial lesions

被引:15
作者
Tsujimoto, Y
Nonomura, N
Takayama, H
Yomogida, K
Nozawa, M
Nishimura, K
Okuyama, A
Nozaki, M
Aozasa, K
机构
[1] Osaka Univ, Sch Med, Dept Sci Lab Anim Experimentat, Microbial Dis Res Inst, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Dept Pathol, Osaka 5650871, Japan
[3] Osaka Univ, Sch Med, Dept Urol, Osaka 5650871, Japan
关键词
Ets family; Gleason score; hPSE; immunohistochemistry; prostatic carcinoma;
D O I
10.1046/j.1442-2042.2002.00444.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Human prostate-specific Ets (hPSE) belongs to the Ets family. It regulates the proliferation, differentiation, and development of prostate epithelial cells. A recent study showed that hPSE can be detected in normal glands but not in cell lines established from prostate cancer (PCA), suggesting a translational disorder of hPSE from mRNA to protein in PCA. Immunohistochemical detection of hPSE could therefore be another method of differential diagnosis of PCA from other proliferative conditions in the prostate. Methods: An immunohistochemical detection of hPSE was carried out on the whole mounted prostatectomy specimen obtained from 19 cases with PCA. Results: Basal and secretory luminar cells showed a diffuse cytoplasmic staining for hPSE in normal glands, hyperplastic glands, and prostate intraepithelial neoplasia lesions. Whereas approximately 30% of PCA lesions showed a negative staining for hPSE, the positive rate for hPSE between PCA and benign glands or prostate intraepithelial neoplasia (PIN), was statistically significant (P < 0.05). Staining intensities in normal glands, hyperplastic glands, and PIN lesions were similar, but generally stronger than those in PCA lesions. Conclusions: Negative immunoreactivity for hPSE strongly suggests malignancy in the prostate glands. Decreased immunoreactivities of glands for hPSE could suggest PCA.
引用
收藏
页码:167 / 172
页数:6
相关论文
共 17 条
[1]  
BOSTWICK DG, 1987, CANCER, V59, P788, DOI 10.1002/1097-0142(19870215)59:4<788::AID-CNCR2820590421>3.0.CO
[2]  
2-I
[3]   GENE FUSION WITH AN ETS DNA-BINDING DOMAIN CAUSED BY CHROMOSOME-TRANSLOCATION IN HUMAN TUMORS [J].
DELATTRE, O ;
ZUCMAN, J ;
PLOUGASTEL, B ;
DESMAZE, C ;
MELOT, T ;
PETER, M ;
KOVAR, H ;
JOUBERT, I ;
DEJONG, P ;
ROULEAU, G ;
AURIAS, A ;
THOMAS, G .
NATURE, 1992, 359 (6391) :162-165
[4]  
Hsing AW, 2000, INT J CANCER, V85, P60, DOI 10.1002/(SICI)1097-0215(20000101)85:1&lt
[5]  
60::AID-IJC11&gt
[6]  
3.0.CO
[7]  
2-B
[8]   UTILIZATION OF HIGH-MOLECULAR-WEIGHT CYTOKERATIN ON PROSTATE NEEDLE BIOPSIES IN AN INDEPENDENT LABORATORY [J].
KAHANE, H ;
SHARP, JW ;
SHUMAN, GB ;
DASILVA, G ;
EPSTEIN, JI .
UROLOGY, 1995, 45 (06) :981-986
[9]   THE ETS-DOMAIN - A NEW DNA-BINDING MOTIF THAT RECOGNIZES A PURINE-RICH CORE DNA-SEQUENCE [J].
KARIM, FD ;
URNESS, LD ;
THUMMEL, CS ;
KLEMSZ, MJ ;
MCKERCHER, SR ;
CELADA, A ;
VANBEVEREN, C ;
MAKI, RA ;
GUNTHER, CV ;
NYE, JA ;
GRAVES, BJ .
GENES & DEVELOPMENT, 1990, 4 (09) :1451-1453
[10]  
Nozawa M, 2000, CANCER RES, V60, P1348