P53 AND KI-67 IMMUNOREACTIVITY IN HUMAN PROSTATE-CANCER AND BENIGN HYPERPLASIA

被引:65
作者
THOMPSON, SJ
MELLON, K
CHARLTON, RG
MARSH, C
ROBINSON, M
NEAL, DE
机构
[1] FREEMAN RD HOSP,DEPT PATHOL,NEWCASTLE TYNE NE7 7DN,TYNE & WEAR,ENGLAND
[2] FREEMAN RD HOSP,DEPT UROL,NEWCASTLE TYNE NE7 7DN,TYNE & WEAR,ENGLAND
[3] FREEMAN RD HOSP,DEPT HISTOPATHOL,NEWCASTLE TYNE NE7 7DN,TYNE & WEAR,ENGLAND
来源
BRITISH JOURNAL OF UROLOGY | 1992年 / 69卷 / 06期
关键词
D O I
10.1111/j.1464-410X.1992.tb15632.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
Mutation of the p53 gene is one of the commonest genetic abnormalities found in solid human tumours. This gene is probably concerned with the control of cellular proliferation and in view of this we carried out a study of human prostate cancer and benign prostatic hyperplasia, comparing the expression of mutated p53 with measurement of growth fractions as assessed by staining with Ki-67. A series of 29 patients with prostate cancer (CaP) were compared with 34 men with benign hyperplasia (BPH); 22 of 29 prostate cancers (76%) contained Ki-67 immunoreactivity compared with 10 of 34 (29%) BPH. With respect to p53 staining, significantly more prostate cancers (1 7%) were stained than BPH (0%). The mean Ki-67 score in cancers positive for p53 (4.3%) was greater than that found in cancers negative for p53 (1.2%), but no statistically significant relationship was found between tumour grade and Ki-67 staining. The use of Ki-67 and p53 staining may allow identification of tumours with a higher rate of cell growth and may permit development of prognostic factors.
引用
收藏
页码:609 / 613
页数:5
相关论文
共 42 条
  • [1] CHROMOSOME-17 DELETIONS AND P53 GENE-MUTATIONS IN COLORECTAL CARCINOMAS
    BAKER, SJ
    FEARON, ER
    NIGRO, JM
    HAMILTON, SR
    PREISINGER, AC
    JESSUP, JM
    VANTUINEN, P
    LEDBETTER, DH
    BARKER, DF
    NAKAMURA, Y
    WHITE, R
    VOGELSTEIN, B
    [J]. SCIENCE, 1989, 244 (4901) : 217 - 221
  • [2] BARTEK J, 1990, ONCOGENE, V5, P893
  • [3] KI67 IMMUNOSTAINING IN PRIMARY BREAST-CANCER - PATHOLOGICAL AND CLINICAL ASSOCIATIONS
    BOUZUBAR, N
    WALKER, KJ
    GRIFFITHS, K
    ELLIS, IO
    ELSTON, CW
    ROBERTSON, JFR
    BLAMEY, RW
    NICHOLSON, RI
    [J]. BRITISH JOURNAL OF CANCER, 1989, 59 (06) : 943 - 947
  • [4] MOUSE P53 INHIBITS SV40 ORIGIN-DEPENDENT DNA-REPLICATION
    BRAITHWAITE, AW
    STURZBECHER, HW
    ADDISON, C
    PALMER, C
    RUDGE, K
    JENKINS, JR
    [J]. NATURE, 1987, 329 (6138) : 458 - 460
  • [5] P53 EXPRESSION IN BREAST-CANCER
    CATTORETTI, G
    RILKE, F
    ANDREOLA, S
    DAMATO, L
    DELIA, D
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1988, 41 (02) : 178 - 183
  • [6] THE P53 PROTO-ONCOGENE CAN ACT AS A SUPPRESSOR OF TRANSFORMATION
    FINLAY, CA
    HINDS, PW
    LEVINE, AJ
    [J]. CELL, 1989, 57 (07) : 1083 - 1093
  • [7] GAETA JF, 1983, SEMINAR UROLOGY, P193
  • [8] GALEE MPW, 1989, J UROLOGY, V142, P1342
  • [9] P53 AND DNA POLYMERASE-ALPHA COMPETE FOR BINDING TO SV40 T-ANTIGEN
    GANNON, JV
    LANE, DP
    [J]. NATURE, 1987, 329 (6138) : 456 - 458
  • [10] ACTIVATING MUTATIONS IN P53 PRODUCE A COMMON CONFORMATIONAL EFFECT - A MONOCLONAL-ANTIBODY SPECIFIC FOR THE MUTANT FORM
    GANNON, JV
    GREAVES, R
    IGGO, R
    LANE, DP
    [J]. EMBO JOURNAL, 1990, 9 (05) : 1595 - 1602