EPIDERMAL GROWTH-FACTOR RECEPTOR EXPRESSION BY NORTHERN ANALYSIS AND IMMUNOHISTOCHEMISTRY IN BENIGN AND MALIGNANT PROSTATIC TUMORS

被引:15
作者
HARPER, ME [1 ]
GODDARD, L [1 ]
GLYNNEJONES, E [1 ]
PEELING, WB [1 ]
GRIFFITHS, K [1 ]
机构
[1] ROYAL GWENT HOSP, DEPT UROL, NEWPORT NP6 2UB, GWENT, WALES
关键词
PROSTATE CARCINOMA; BPH; IMMUNOHISTOCHEMICAL; MESSENGER-RNA ANALYSIS; PEPTIDE GROWTH FACTOR RECEPTOR; EGF RECEPTOR;
D O I
10.1016/0959-8049(95)00207-Y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidermal growth factor receptor (EGFR) expression in 44 benign prostatic hyperplasia (BPH) and 55 prostatic carcinoma specimens has been investigated using Northern blot analysis and immunohistochemistry. The values obtained for the EGFR mRNA in the BPH and carcinoma specimens were not significantly different and in the latter there was no correlation with grade. In the immunohistochemical assays, two antibodies to the external and one to the internal domain of EGFR were used. The former ones stained the basal cell membranes intensely whilst cytoplasmic staining of secretory epithelium was seen in BPH specimens with the latter. In the carcinoma specimens, the intensity of membrane staining correlated with the two external domain antibodies, r = 0.640, P<0.001, but neither of these correlated with the EGFR mRNA results. All three antibodies demonstrated a trend towards elevated expression of EGFR with dedifferentiation which reached significance only with the internal domain antibody results, P<0.02. No correlation was observed with tumour EGFR mRNA values and the EGFR immunohistochemical results. The EGFR immunoreaction with the external domain antibody in 14 treated high-grade tumours was comparable to that obtained in 15 untreated anaplastic prostatic tumours. In 5 patients, both pre- and post-treatment samples were available and these exhibited little or no difference in EGFR expression with therapy.
引用
收藏
页码:1492 / 1497
页数:6
相关论文
共 28 条
  • [1] SECRETION OF EPIDERMAL GROWTH-FACTOR AND RELATED POLYPEPTIDES BY THE DU-145 HUMAN-PROSTATE CANCER CELL-LINE
    CONNOLLY, JM
    ROSE, DP
    [J]. PROSTATE, 1989, 15 (02) : 177 - 186
  • [2] AUTOCRINE REGULATION OF DU145 HUMAN PROSTATE-CANCER CELL-GROWTH BY EPIDERMAL GROWTH FACTOR-RELATED POLYPEPTIDES
    CONNOLLY, JM
    ROSE, DP
    [J]. PROSTATE, 1991, 19 (02) : 173 - 180
  • [3] PRODUCTION OF EPIDERMAL GROWTH-FACTOR AND TRANSFORMING GROWTH FACTOR-ALPHA BY THE ANDROGEN-RESPONSIVE LNCAP HUMAN PROSTATE-CANCER CELL-LINE
    CONNOLLY, JM
    ROSE, DP
    [J]. PROSTATE, 1990, 16 (03) : 209 - 218
  • [4] DAVIS LG, 1986, BASIC METHODS MOL BI, P130
  • [5] GROWTH-FACTOR INVOLVEMENT AND ONCOGENE EXPRESSION IN PROSTATIC TUMORS
    EATON, CL
    DAVIES, P
    PHILLIPS, MEA
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1988, 30 (1-6) : 341 - 345
  • [6] GROWTH-FACTORS IN THE HUMAN PROSTATE
    FIORELLI, G
    DEBELLIS, A
    LONGO, A
    PIOLI, P
    COSTANTINI, A
    GIANNINI, S
    FORTI, G
    SERIO, M
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 40 (1-3) : 199 - 205
  • [7] FONG CJ, 1992, CANCER RES, V52, P5887
  • [8] EPIDERMAL GROWTH-FACTOR AND PROSTATIC-CARCINOMA - AN IMMUNOHISTOCHEMICAL STUDY
    FOWLER, JE
    LAU, JLT
    GHOSH, L
    MILLS, SE
    MOUNZER, A
    [J]. JOURNAL OF UROLOGY, 1988, 139 (04) : 857 - 861
  • [9] TRANSFORMING GROWTH-FACTOR-BETA-1 EXPRESSION IN BENIGN AND MALIGNANT PROSTATIC TUMORS
    GLYNNEJENES, E
    HARPER, ME
    GODDARD, L
    EATON, CL
    MATTHEWS, PN
    GRIFFITHS, K
    [J]. PROSTATE, 1994, 25 (04) : 210 - 218
  • [10] GLYNNEJONES E, 1992, PROSTATE, V20, P133