Concordance between p53 protein overexpression and gene mutation in a large series of common human carcinomas

被引:148
作者
Soong, R
Robbins, PD
Dix, BR
Grieu, F
Lim, B
Knowles, S
Williams, KE
Turbett, GR
House, AK
Iacopetta, BJ
机构
[1] UNIV WESTERN AUSTRALIA,DEPT SURG,NEDLANDS,WA 6907,AUSTRALIA
[2] KING EDWARD MEM HOSP WOMEN,DEPT PATHOL,SUBIACO,WA 6008,AUSTRALIA
[3] WESTERN AUSTRALIAN CTR PATHOL & MED RES,DEPT ANAT PATHOL,NEDLANDS,WA,AUSTRALIA
[4] ROYAL PERTH HOSP,DEPT PATHOL,PERTH,WA,AUSTRALIA
关键词
p53; mutation; colorectal cancer; breast cancer; endometrial cancer; gastric cancer;
D O I
10.1016/S0046-8177(96)90282-8
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Immunohistochemical (IHC) detection of p53 protein was com pared with the presence of P53 gene mutation in many colorectal (n = 100), breast (n = 92), endometrial (n = 122), and gastric (n = 116) carcinomas. Two commercially available antibodies, DO7 and CM1, were used for MC analysis of paraffin-embedded tissue sections. Screening for gene mutations in frozen and paraffin-embedded tumor samples was carried out using polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP). The frequency of nuclear staining with DO7 or CM1 for each tumor type, respectively was colorectal (36%, 23%); breast (15%, 19%); endometrial (21%, 33%), and gastric (23%,-). Overall correlation between the two antibodies for nuclear staining was 90% for the 314 tumors analyzed. Cytoplasmic staining was observed with DO7 in 17% of breast and 5% of gastric carcinomas and with CM1 in 17% of breast and 54% of endometrial carcinomas. p53 gene mutation was found in 39% of colorectal, 28% of breast, 13% of endometrial, and 25% of gastric cancers. The concordance between p53 nuclear overexpression and gene mutation (both positive or both negative) was 68% for colorectal, 79% for breast, 76% for endometrial, and 73% for gastric carcinomas. This study provides further evidence that MC detection of p53 protein accumulation does not always indicate the presence of a gene mutation and vice versa. Discordant results were observed in approximately 20% to 30% of the tumors studied, highlighting the need for careful characterization of both p53 gene and protein alterations when assessing the relationship between p53 status and tumor behavior. Copyright (C) 1996 by W.B. Saunders Company
引用
收藏
页码:1050 / 1055
页数:6
相关论文
共 48 条
  • [1] MUTATION AND EXPRESSION OF THE P53 GENE IN HUMAN-MALIGNANT MELANOMA
    ALBINO, AP
    VIDAL, MJ
    MCNUTT, NS
    SHEA, CR
    PRIETO, VG
    NANUS, DM
    PALMER, JM
    HAYWARD, NK
    [J]. MELANOMA RESEARCH, 1994, 4 (01) : 35 - 45
  • [2] ASSOCIATION OF P53 PROTEIN EXPRESSION WITH TUMOR-CELL PROLIFERATION RATE AND CLINICAL OUTCOME IN NODE-NEGATIVE BREAST-CANCER
    ALLRED, DC
    CLARK, GM
    ELLEDGE, R
    FUQUA, SAW
    BROWN, RW
    CHAMNESS, GC
    OSBORNE, CK
    MCGUIRE, WL
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (03) : 200 - 206
  • [3] PROGNOSTIC-SIGNIFICANCE OF TP53 ALTERATIONS IN BREAST-CARCINOMA
    ANDERSEN, TI
    HOLM, R
    NESLAND, JM
    HEIMDAL, KR
    OTTESTAD, L
    BORRESEN, AL
    [J]. BRITISH JOURNAL OF CANCER, 1993, 68 (03) : 540 - 548
  • [4] P53 PROTEIN ALTERATIONS IN HUMAN TESTICULAR CANCER INCLUDING PREINVASIVE INTRATUBULAR GERM-CELL NEOPLASIA
    BARTKOVA, J
    BARTEK, J
    LUKAS, J
    VOJTESEK, B
    STASKOVA, Z
    REJTHAR, A
    KOVARIK, J
    MIDGLEY, CA
    LANE, DP
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1991, 49 (02) : 196 - 202
  • [5] P53 IMMUNOHISTOCHEMISTRY - A WORD OF CAUTION
    BATTIFORA, H
    [J]. HUMAN PATHOLOGY, 1994, 25 (05) : 435 - 437
  • [6] PROGNOSTIC VALUE OF P53 OVEREXPRESSION AND C-KI-RAS GENE-MUTATIONS IN COLORECTAL-CANCER
    BELL, SM
    SCOTT, N
    CROSS, D
    SAGAR, P
    LEWIS, FA
    BLAIR, GE
    TAYLOR, GR
    DIXON, MF
    QUIRKE, P
    [J]. GASTROENTEROLOGY, 1993, 104 (01) : 57 - 64
  • [7] CYTOPLASMIC ACCUMULATION OF P53 PROTEIN - AN INDEPENDENT PROGNOSTIC INDICATOR IN COLORECTAL ADENOCARCINOMAS
    BOSARI, S
    VIALE, G
    BOSSI, P
    MAGGIONI, M
    COGGI, G
    MURRAY, JJ
    LEE, AKC
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (09): : 681 - 687
  • [8] BOSARI S, 1995, AM J PATHOL, V147, P7908
  • [9] CARBONE DP, 1993, P AN M AM SOC CLIN, V12, pA1112
  • [10] CESARMAN E, 1993, AM J PATHOL, V143, P845