MOLECULAR AND IMMUNOHISTOCHEMICAL ANALYSIS OF P53 IN PHEOCHROMOCYTOMA

被引:26
作者
DAHIA, PLM
AGUIAR, RCT
TSANACLIS, AM
BENDIT, I
BYDLOWSKI, SP
ABELIN, NMA
TOLEDO, SPA
机构
[1] UNIV SAO PAULO,SCH MED,DIV ENDOCRINOL,ENDOCRINE GENET UNIT,BR-05508 SAO PAULO,BRAZIL
[2] UNIV SAO PAULO,SCH MED,DIV HAEMATOL,BR-05508 SAO PAULO,BRAZIL
[3] UNIV SAO PAULO,SCH MED,DEPT PATHOL,BR-05508 SAO PAULO,BRAZIL
基金
巴西圣保罗研究基金会;
关键词
PHEOCHROMOCYTOMA; P53; GENE; MUTATION; IMMUNOHISTOCHEMISTRY; MOLECULAR SCREENING; POLYMORPHISM;
D O I
10.1038/bjc.1995.487
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We searched for mutations of the p53 gene in 25 phaeochromocytomas using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) analysis of the entire conserved region of the gene, encompassing exons 4-8; expression of the p53 protein was assessed by immunohistochemistry. No mutations were found, while a polymorphism in codon 72 was observed. Immunohistochemistry revealed nuclear p53 overexpression in one tumour sample. We conclude that mutations of the 'hotspot' region of the p53 gene do not seem to play a role in the pathogenesis of phaeochromocytoma.
引用
收藏
页码:1211 / 1213
页数:3
相关论文
共 19 条
  • [1] AGUJAR RCT, 1995, IN PRESS CANCER GENE
  • [2] BODNER SM, 1992, ONCOGENE, V7, P743
  • [3] P53 MUTATIONS IN HUMAN CANCERS
    HOLLSTEIN, M
    SIDRANSKY, D
    VOGELSTEIN, B
    HARRIS, CC
    [J]. SCIENCE, 1991, 253 (5015) : 49 - 53
  • [4] LOSS OF HETEROZYGOSITY SUGGESTS MULTIPLE GENETIC ALTERATIONS IN PHEOCHROMOCYTOMAS AND MEDULLARY-THYROID CARCINOMAS
    KHOSLA, S
    PATEL, VM
    HAY, ID
    SCHAID, DJ
    GRANT, CS
    VANHEERDEN, JA
    THIBODEAU, SN
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (05) : 1691 - 1699
  • [5] CANCER - A DEATH IN THE LIFE OF P53
    LANE, DP
    [J]. NATURE, 1993, 362 (6423) : 786 - 787
  • [6] IDENTIFICATION OF THE VONHIPPEL-LINDAU DISEASE TUMOR-SUPPRESSOR GENE
    LATIF, F
    TORY, K
    GNARRA, J
    YAO, M
    DUH, FM
    ORCUTT, ML
    STACKHOUSE, T
    KUZMIN, I
    MODI, W
    GEIL, L
    SCHMIDT, L
    ZHOU, FW
    LI, H
    WEI, MH
    CHEN, F
    GLENN, G
    CHOYKE, P
    WALTHER, MM
    WENG, YK
    DUAN, DSR
    DEAN, M
    GLAVAC, D
    RICHARDS, FM
    CROSSEY, PA
    FERGUSONSMITH, MA
    LEPASLIER, D
    CHUMAKOV, I
    COHEN, D
    CHINAULT, AC
    MAHER, ER
    LINEHAN, WM
    ZBAR, B
    LERMAN, MI
    [J]. SCIENCE, 1993, 260 (5112) : 1317 - 1320
  • [7] MUTATIONS OF THE P53 GENE IN HUMAN FUNCTIONAL ADRENAL NEOPLASMS
    LIN, SR
    LEE, YJ
    TSAI, JH
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (02) : 483 - 491
  • [8] LINNOILA RI, 1990, HUM PATHOL, V21, P1168
  • [9] PRIMARY STRUCTURE POLYMORPHISM AT AMINO-ACID RESIDUE-72 OF HUMAN-P53
    MATLASHEWSKI, GJ
    TUCK, S
    PIM, D
    LAMB, P
    SCHNEIDER, J
    CRAWFORD, LV
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (02) : 961 - 963
  • [10] THE MDM-2 ONCOGENE PRODUCT FORMS A COMPLEX WITH THE P53 PROTEIN AND INHIBITS P53-MEDIATED TRANSACTIVATION
    MOMAND, J
    ZAMBETTI, GP
    OLSON, DC
    GEORGE, D
    LEVINE, AJ
    [J]. CELL, 1992, 69 (07) : 1237 - 1245