Expression of p21(waf1/Cip1), MDM2 and p53 in vivo: Analysis of cytological preparations

被引:5
作者
Dowell, SP
McGoogan, E
Picksley, SM
ElDeiry, WS
Vogelstein, B
Hall, PA
机构
[1] UNIV DUNDEE,DEPT MOL & CELLULAR BIOL,DUNDEE DD1 9SY,SCOTLAND
[2] UNIV DUNDEE,DEPT BIOCHEM,CRC,CELL TRANSFORMAT GRP,DUNDEE DD1 9SY,SCOTLAND
[3] UNIV EDINBURGH,DEPT PATHOL,EDINBURGH,MIDLOTHIAN,SCOTLAND
[4] UNIV PENN,HOWARD HUGHES MED INST,PHILADELPHIA,PA 19104
[5] UNIV PENN,SCH MED,DEPT MED,PHILADELPHIA,PA 19104
[6] UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
[7] JOHNS HOPKINS UNIV,SCH MED,JOHNS HOPKINS ONCOL CTR,GENET MOL LAB,BALTIMORE,MD 21205
关键词
p21(waf1/Cip1); p53; MDM2; immunohistochemistry; cytology; reactive mesothelium;
D O I
10.1111/j.1365-2303.1996.tb00313.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of this study was to test the hypothesis that expression of p21(waf1/Cip1) and MDM2 could be used as indicators of the activity of wild-type p53 which can transcriptionally activate the p21(waf1/Cip1) and mdm2 genes. In cytological preparations of serous fluids, the expression of p53, p21(waf1/Cip1) and MDM2 protein was assessed by immunohistochemistry. A series of 50 cases was assessed for both p53 and p21(waf1/Cip1) expression and a subset of 37 cases had sufficient material for analysis of MDM2. In samples in which there were reactive mesothelial cells (n=48) there was general concordance between p53 and p21(waf1/Cip1) expression, but in nine cases p21(waf1/Cip1) was expressed in the absence of detectable p53. Similarly, MDM2 expression was not correlated with p53 in 15 of 31 cases. p21(waf1/Cip1) was correlated with MDM2 in 24 of 31 cases, while in the remaining seven, MDM2 was expressed without detectable p21(waf1/Cip1) immunoreactivity. In samples with neoplastic cells (n=18) the presence of p21(waf1/Cip1) and MDM2 expression was always associated with p53 expression. Polymorphonuclear leucocytes frequently showed p21(waf1/Cip1) immunoreactivity, and this was confirmed by immunoblotting of peripheral blood polymorphonuclear leucocytes. These data indicate that in general p21(waf1/Cip1) expression correlates with p53 expression in reactive mesothelial cells, consistent with a known mechanism of regulation. However, in reactive mesothelial cells, MDM2 expression is perhaps dissociated from p53 expression, contrary to current models of MDM2 regulation. Finally, in addition to many normal tissues, it is likely that in reactive mesothelial cells and some tumours p21(waf1/Cip1) expression is not dependent on the presence of wild-type p53 protein. In conclusion, p53 status cannot be reliably predicted based only on p21(waf1/Cip1) or MDM2 expression.
引用
收藏
页码:340 / 351
页数:12
相关论文
共 57 条
  • [1] MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY
    BARAK, Y
    JUVEN, T
    HAFFNER, R
    OREN, M
    [J]. EMBO JOURNAL, 1993, 12 (02) : 461 - 468
  • [2] P53-DEPENDENT APOPTOSIS IN THE ABSENCE OF TRANSCRIPTIONAL ACTIVATION OF P53-TARGET GENES
    CAELLES, C
    HELMBERG, A
    KARIN, M
    [J]. NATURE, 1994, 370 (6486) : 220 - 223
  • [3] THYMOCYTE APOPTOSIS INDUCED BY P53-DEPENDENT AND INDEPENDENT PATHWAYS
    CLARKE, AR
    PURDIE, CA
    HARRISON, DJ
    MORRIS, RG
    BIRD, CC
    HOOPER, ML
    WYLLIE, AH
    [J]. NATURE, 1993, 362 (6423) : 849 - 852
  • [4] CONTROL OF ANGIOGENESIS IN FIBROBLASTS BY P53 REGULATION OF THROMBOSPONDIN-1
    DAMERON, KM
    VOLPERT, OV
    TAINSKY, MA
    BOUCK, N
    [J]. SCIENCE, 1994, 265 (5178) : 1582 - 1584
  • [5] EXPRESSION OF P53 IN REACTIVE MESOTHELIUM
    DOWELL, S
    DERIAS, N
    WILSON, POG
    LANE, DP
    HALL, PA
    [J]. HISTOPATHOLOGY, 1993, 22 (01) : 96 - 97
  • [6] THE CLINICAL RELEVANCE OF THE P53 TUMOR-SUPPRESSOR GENE
    DOWELL, SP
    HALL, PA
    [J]. CYTOPATHOLOGY, 1994, 5 (03) : 133 - 145
  • [7] DOWELL SP, 1994, CANCER RES, V54, P2914
  • [8] P53-DEPENDENT INHIBITION OF CYCLIN-DEPENDENT KINASE-ACTIVITIES IN HUMAN FIBROBLASTS DURING RADIATION-INDUCED G1 ARREST
    DULIC, V
    KAUFMANN, WK
    WILSON, SJ
    TLSTY, TD
    LEES, E
    HARPER, JW
    ELLEDGE, SJ
    REED, SI
    [J]. CELL, 1994, 76 (06) : 1013 - 1023
  • [9] DEFINITION OF A CONSENSUS BINDING-SITE FOR P53
    ELDEIRY, WS
    KERN, SE
    PIETENPOL, JA
    KINZLER, KW
    VOGELSTEIN, B
    [J]. NATURE GENETICS, 1992, 1 (01) : 45 - 49
  • [10] ELDEIRY WS, 1994, CANCER RES, V54, P1169