TY - JOUR
T1 - CTNNB1 mutations and overexpression of Wnt/β-catenin target genes in WT1-mutant wilms' tumors
AU - Li, Chi Ming
AU - Kim, Connie E.
AU - Margolin, Adam A.
AU - Guo, Meirong
AU - Zhu, Jimmy
AU - Mason, Jacqueline M.
AU - Hensle, Terrence W.
AU - Murty, Vundavalli V.V.S.
AU - Grundy, Paul E.
AU - Fearon, Eric R.
AU - D'Agati, Vivette
AU - Licht, Jonathan D.
AU - Tycko, Benjamin
N1 - Funding Information:
Supported by grants from the National Institutes of Health (to J.D.L. and B.T.) and the Stewart Trust (to B.T.).
PY - 2004/12
Y1 - 2004/12
N2 - Gain-of-function mutations in exon 3 of β-catenin (CTNNB1) are specific for Wilms' tumors that have lost WT1, but 50% of WT1-mutant cases lack such "hot spot" mutations. To ask whether stabilization of β-catenin might be essential after WT1 loss, and to identify downstream target genes, we compared expression profiles in WT1-mutant versus WT1 wild-type Wilms' tumors. Supervised and nonsupervised hierarchical clustering of the expression data separated these two classes of Wilms' tumor. The WT1-mutant tumors overexpressed genes encoding myogenic and other transcription factors (MOX2, LBX1, SIM2), signalling molecules (TGFB2, FST, BMP2A), extracellular Wnt inhibitors (WIF1, SFRP4), and known β-catenin/TCF targets (FST, CSPG2, CMYC). β-Catenin/TCF target genes were overexpressed in the WT1-mutant tumors even in the absence of CTNNB1 exon 3 mutations, and complete sequencing revealed gain-of-function mutations elsewhere in the CTNNB1 gene to some of these tumors, increasing the overall mutation frequency to 75%. Lastly, we identified and validated a novel direct β-catenin target gene, GAD1, among the WT1-mutant signature genes. These data highlight two molecular classes of Wilms' tumor, and indicate strong selection for stabilization of β-catenin in the WT1-mutant class. β-Catenin stabilization can initiate tumorigenesis in other systems, and this mechanism is likely critical in tumor formation after loss of WT1.
AB - Gain-of-function mutations in exon 3 of β-catenin (CTNNB1) are specific for Wilms' tumors that have lost WT1, but 50% of WT1-mutant cases lack such "hot spot" mutations. To ask whether stabilization of β-catenin might be essential after WT1 loss, and to identify downstream target genes, we compared expression profiles in WT1-mutant versus WT1 wild-type Wilms' tumors. Supervised and nonsupervised hierarchical clustering of the expression data separated these two classes of Wilms' tumor. The WT1-mutant tumors overexpressed genes encoding myogenic and other transcription factors (MOX2, LBX1, SIM2), signalling molecules (TGFB2, FST, BMP2A), extracellular Wnt inhibitors (WIF1, SFRP4), and known β-catenin/TCF targets (FST, CSPG2, CMYC). β-Catenin/TCF target genes were overexpressed in the WT1-mutant tumors even in the absence of CTNNB1 exon 3 mutations, and complete sequencing revealed gain-of-function mutations elsewhere in the CTNNB1 gene to some of these tumors, increasing the overall mutation frequency to 75%. Lastly, we identified and validated a novel direct β-catenin target gene, GAD1, among the WT1-mutant signature genes. These data highlight two molecular classes of Wilms' tumor, and indicate strong selection for stabilization of β-catenin in the WT1-mutant class. β-Catenin stabilization can initiate tumorigenesis in other systems, and this mechanism is likely critical in tumor formation after loss of WT1.
UR - http://www.scopus.com/inward/record.url?scp=9644265525&partnerID=8YFLogxK
U2 - 10.1016/S0002-9440(10)63246-4
DO - 10.1016/S0002-9440(10)63246-4
M3 - Article
C2 - 15579438
AN - SCOPUS:9644265525
SN - 0002-9440
VL - 165
SP - 1943
EP - 1953
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 6
ER -