The role of WT1 in oncogenesis: Tumor suppressor or oncogene?

被引:50
作者
Loeb, DM [1 ]
Sukumar, S [1 ]
机构
[1] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
关键词
leukemia; Wilms' tumor; breast cancer; mesothelioma; transcription factor;
D O I
10.1007/BF02982573
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although originally identified as a tumor suppressor gene, WT1 is overexpressed in a variety of hematologic malignancies and solid tumors, including acute leukemia, breast cancer, malignant mesothelioma, renal cell carcinoma, and others. Overexpression of both wild-type and mutant WT1 has been reported. In some cases, this finding represents overexpression of a gene that should be expressed at lower levels, but in other cases, WT1 is expressed at high levels in a tissue type in which there is normally no expression at all. In this review, the mechanisms of altered WT1 expression are explored, including changes in promoter methylation. WT1 target genes that may be important for oncogenesis are discussed, as is the use of WT1 expression as a diagnostic tool. The prognostic implications of altered WT1 expression and the potential for immunotherapy aimed at WT1 are also discussed.
引用
收藏
页码:117 / 126
页数:10
相关论文
共 116 条
  • [31] HUMAN PLATELET-DERIVED GROWTH FACTOR-A CHAIN IS TRANSCRIPTIONALLY REPRESSED BY THE WILMS-TUMOR SUPPRESSOR WT1
    GASHLER, AL
    BONTHRON, DT
    MADDEN, SL
    RAUSCHER, FJ
    COLLINS, T
    SUKHATME, VP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) : 10984 - 10988
  • [32] Clinical, pathologic, and molecular spectrum of tumors associated with t(11;22)(p13;q12): Desmoplastic small round-cell tumor and its variants
    Gerald, WL
    Ladanyi, M
    de Alava, E
    Cuatrecasas, M
    Kushner, BH
    LaQuaglia, MP
    Rosai, J
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (09) : 3028 - 3036
  • [33] CHARACTERIZATION OF THE GENOMIC BREAKPOINT AND CHIMERIC TRANSCRIPTS IN THE EWS-WT1 GENE FUSION OF DESMOPLASTIC SMALL ROUND-CELL TUMOR
    GERALD, WL
    ROSAI, J
    LADANYI, L
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (04) : 1028 - 1032
  • [34] HOMOZYGOUS DELETION IN WILMS-TUMORS OF A ZINC-FINGER GENE IDENTIFIED BY CHROMOSOME JUMPING
    GESSLER, M
    POUSTKA, A
    CAVENEE, W
    NEVE, RL
    ORKIN, SH
    BRUNS, GAP
    [J]. NATURE, 1990, 343 (6260) : 774 - 778
  • [35] Goldstein NS, 2002, AM J CLIN PATHOL, V117, P541
  • [36] Goldstein NS, 2001, AM J CLIN PATHOL, V116, P246
  • [37] GOODYER P, 1995, ONCOGENE, V10, P1125
  • [38] CHROMOSOME-11 UNIPARENTAL ISODISOMY PREDISPOSING TO EMBRYONAL NEOPLASMS
    GRUNDY, P
    TELZEROW, P
    PATERSON, MC
    HABER, D
    BERMAN, B
    LI, F
    GARBER, J
    [J]. LANCET, 1991, 338 (8774) : 1079 - 1080
  • [39] Induction of Rb-associated protein (RbAp46) by Wilms' tumor suppressor WT1 mediates growth inhibition
    Guan, LS
    Rauchman, M
    Wang, ZY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) : 27047 - 27050
  • [40] WT1-MEDIATED GROWTH SUPPRESSION OF WILMS-TUMOR CELLS EXPRESSING A WT1 SPLICING VARIANT
    HABER, DA
    PARK, S
    MAHESWARAN, S
    ENGLERT, C
    RE, GG
    HAZENMARTIN, DJ
    SENS, DA
    GARVIN, AJ
    [J]. SCIENCE, 1993, 262 (5142) : 2057 - 2059