TARGET GENES OF THE WILMS' TUMOUR SUPPRESSOR GENE AS IDENTIFIED BY cDNA EXPRESSION PROFILING

Nephrology ◽  
2002 ◽  
Vol 7 (1) ◽  
pp. A5-A5
Author(s):  
Little M.H ◽  
Forrest A ◽  
Grimmond S ◽  
Lindsay M ◽  
Martinez G ◽  
...  
Gene ◽  
1995 ◽  
Vol 167 (1-2) ◽  
pp. 239-243 ◽  
Author(s):  
Andrew Ward ◽  
Jo-Anna Pooler ◽  
Kiyoshi Miyagawa ◽  
Antonio Duarte ◽  
Nicholas D. Hastie ◽  
...  

Oncogene ◽  
1997 ◽  
Vol 14 (22) ◽  
pp. 2689-2700 ◽  
Author(s):  
Melanie J McConnell ◽  
Heather E Cunliffe ◽  
Lin J Chua ◽  
Teresa A Ward ◽  
Michael R Eccles

Oncogene ◽  
2002 ◽  
Vol 21 (47) ◽  
pp. 7277-7282 ◽  
Author(s):  
Kate J Wagner ◽  
Wendy N Cooper ◽  
Richard G Grundy ◽  
Germaine Caldwell ◽  
Carolyn Jones ◽  
...  

2008 ◽  
Vol 36 (4) ◽  
pp. 629-631 ◽  
Author(s):  
Jörg Hartkamp ◽  
Stefan G.E. Roberts

The Wilms' tumour-suppressor gene (WT1), encodes a zinc-finger transcription factor that is critical for the development of several organs, including the kidneys, gonads and spleen. Despite its identification as a tumour suppressor that plays a crucial role in the formation of a paediatric malignancy of the kidneys (Wilms' tumour), it has also emerged as an oncogenic factor influencing proliferation and apoptosis in a large variety of adult cancers. This review focuses on new insights into WT1's role in early development and its potential oncogenic role in adult cancer.


1998 ◽  
Vol 72 (1) ◽  
pp. 59-72
Author(s):  
A. MOORE ◽  
A. SCHEDL ◽  
L. McINNES ◽  
J. KREIDBERG ◽  
R. JAENISCH ◽  
...  

2009 ◽  
Vol 422 (3) ◽  
pp. 543-551 ◽  
Author(s):  
Hanshao Liu ◽  
Hoi Chin Hew ◽  
Zheng-Guang Lu ◽  
Tomoko Yamaguchi ◽  
Yoshio Miki ◽  
...  

Transcriptional regulation of the p53 tumour suppressor gene plays an important role in the control of the expression of various target genes involved in the DNA damage response. However, the molecular basis of this regulation remains obscure. In the present study we demonstrate that RREB-1 (Ras-responsive-element-binding protein-1) efficiently binds to the p53 promoter via the p53 core promoter element and transactivates p53 expression. Silencing of RREB-1 significantly reduces p53 expression at both the mRNA and the protein levels. Notably, disruption of RREB-1-mediated p53 transcription suppresses the expression of the p53 target genes. We also show that, upon exposure to genotoxic stress, RREB-1 controls apoptosis in a p53-dependent manner. These findings provide evidence that RREB-1 participates in modulating p53 transcription in response to DNA damage.


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