共 112 条
Wilms' tumours: about tumour suppressor genes, an oncogene and a chameleon gene
被引:190
作者:

Huff, Vicki
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas MD Anderson Canc Ctr, Dept Genet, Unit 1010, Houston, TX 77030 USA
UT Houston Grad Sch Biomed Sci, Grad Program Genes & Dev, Houston, TX 77025 USA
UT Houston Grad Sch Biomed Sci, Grad Program Human Mol Genet, Houston, TX 77025 USA Univ Texas MD Anderson Canc Ctr, Dept Genet, Unit 1010, Houston, TX 77030 USA
机构:
[1] Univ Texas MD Anderson Canc Ctr, Dept Genet, Unit 1010, Houston, TX 77030 USA
[2] UT Houston Grad Sch Biomed Sci, Grad Program Genes & Dev, Houston, TX 77025 USA
[3] UT Houston Grad Sch Biomed Sci, Grad Program Human Mol Genet, Houston, TX 77025 USA
关键词:
ACUTE MYELOID-LEUKEMIA;
BECKWITH-WIEDEMANN-SYNDROME;
HEMATOPOIETIC PROGENITOR CELLS;
MINIMAL RESIDUAL DISEASE;
EARLY KIDNEY DEVELOPMENT;
WT1;
MESSENGER-RNA;
BETA-CATENIN;
NEPHROGENIC RESTS;
PROGNOSTIC-SIGNIFICANCE;
WILMS-TUMOR-1;
GENE;
D O I:
10.1038/nrc3002
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Genes identified as being mutated in Wilms' tumour include TP53, a classic tumour suppressor gene (TSG); CTNNB1 (encoding beta-catenin), a classic oncogene; WTX, which accumulating data indicate is a TSG; and WT1, which is inactivated in some Wilms' tumours, similar to a TSG. However, WT1 does not always conform to the TSG label, and some data indicate that WT1 enhances cell survival and proliferation, like an oncogene. Is WT1 a chameleon, functioning as either a TSG or an oncogene, depending on cellular context? Are these labels even appropriate for describing and understanding the function of WT1?
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页码:111 / 121
页数:11
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