DIFFERENTIAL IMMUNOREACTIVITY OF EPIDERMAL GROWTH-FACTOR RECEPTOR IN BENIGN, DYSPLASTIC AND MALIGNANT PROSTATIC TISSUES

被引:68
作者
IBRAHIM, GK
KERNS, BJM
MACDONALD, JA
IBRAHIM, SN
KINNEY, RB
HUMPHREY, PA
ROBERTSON, CN
机构
[1] DUKE UNIV,MED CTR,DUKE COMPREHENS CANC CTR,DEPT PATHOL,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DUKE COMPREHENS CANC CTR,DIV UROL,DURHAM,NC 27710
关键词
GROWTH FACTORS; PROSTATE; PROSTATIC HYPERTROPHY;
D O I
10.1016/S0022-5347(17)36032-9
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
To investigate epidermal growth factor receptor (EGFr) presence in the prostate, monoclonal antibody (clone EGFR1) immunohistochemical examination of radical prostatectomy specimens was performed (n = 37). All prostatic specimens contained benign prostatic hyperplasia (BPH) and/or dysplasia (prostatic intraepithelial neoplasia or PIN), as well as prostatic carcinoma (CaP). Areas of dysplasia were further categorized as to the basal cell layer and the luminal cell area. BPH, PIN, and CaP tissues in each specimen were analyzed by a single observer and graded on a scale from 0-4+. Fifteen samples were also analyzed for EGFr content utilizing a Cell Analysis Systems (CAS 200) image cytometer. EGFr immunoreactivity of BPH basal cells was significantly higher than EGFr immunoreactivity in areas of CaP (p <0.001). EGFr staining of BPH basal cells was also significantly higher than that seen in PIN luminal cells (p <0.001). Immunoreactivity of EGFr in PIN basal cells was significantly higher than in PIN luminal cells (p <0.001). EGFr staining of basal cells in BPH tissues was higher than that seen in the PIN basal cell layer but the difference was not statistically significant (p = 0.06). The amount of staining present in PIN luminal cells was also significantly greater than in CaP tissues (p = 0.002). Quantitative image analysis utilizing the CAS 200 image cytometer was performed on BPH and CaP areas exclusively. EGFr immunoreactivity in basal cells of the BPH tissues was significantly greater than that seen in CaP tissues (p <0.001). The decreased EGFr immunoreactivity in CaP may reflect a differentiating role for EGFr in normal tissues. Loss of EGFr influence may be associated with an increased proliferative state in PIN and CaP. Destruction or alteration of the epidermal growth factor receptor by a protease, such as prostatic specific antigen, may also explain our findings. At the present time the meaning of the different amounts of EGFr in the various types of prostate tissues is unknown.
引用
收藏
页码:170 / 173
页数:4
相关论文
共 18 条
[1]  
BACUS SS, 1990, ARCH PATHOL LAB MED, V114, P164
[2]  
BOSTWICK DG, 1987, CANCER, V59, P788, DOI 10.1002/1097-0142(19870215)59:4<788::AID-CNCR2820590421>3.0.CO
[3]  
2-I
[4]   EPIDERMAL GROWTH-FACTOR [J].
CARPENTER, G ;
COHEN, S .
ANNUAL REVIEW OF BIOCHEMISTRY, 1979, 48 :193-216
[5]  
COHEN S, 1962, J BIOL CHEM, V237, P1555
[6]   HUMAN EPIDERMAL GROWTH-FACTOR - ISOLATION AND CHEMICAL AND BIOLOGICAL PROPERTIES [J].
COHEN, S ;
CARPENTER, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (04) :1317-1321
[7]   TYROSINE KINASE RECEPTOR WITH EXTENSIVE HOMOLOGY TO EGF RECEPTOR SHARES CHROMOSOMAL LOCATION WITH NEU ONCOGENE [J].
COUSSENS, L ;
YANGFENG, TL ;
LIAO, YC ;
CHEN, E ;
GRAY, A ;
MCGRATH, J ;
SEEBURG, PH ;
LIBERMANN, TA ;
SCHLESSINGER, J ;
FRANCKE, U ;
LEVINSON, A ;
ULLRICH, A .
SCIENCE, 1985, 230 (4730) :1132-1139
[8]  
DAMJANOV I, 1986, LAB INVEST, V55, P558
[9]   GROWTH-FACTOR RECEPTORS AND ONCOGENE EXPRESSION IN PROSTATE CELLS [J].
DAVIES, P ;
EATON, CL ;
FRANCE, TD ;
PHILLIPS, MEA .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1988, 11 :S1-S7
[10]   GROWTH-FACTOR INVOLVEMENT AND ONCOGENE EXPRESSION IN PROSTATIC TUMORS [J].
EATON, CL ;
DAVIES, P ;
PHILLIPS, MEA .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1988, 30 (1-6) :341-345