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Deregulated WNT Signaling in Childhood T-cell Acute Lymphoblastic Leukemia

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Journal Blood Cancer J
Date 2014 Mar 18
PMID 24632884
Citations 33
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Abstract

WNT signaling has been implicated in the regulation of hematopoietic stem cells and plays an important role during T-cell development in thymus. Here we investigated WNT pathway activation in childhood T-cell acute lymphoblastic leukemia (T-ALL) patients. To evaluate the potential role of WNT signaling in T-cell leukomogenesis, we performed expression analysis of key components of WNT pathway. More than 85% of the childhood T-ALL patients showed upregulated β-catenin expression at the protein level compared with normal human thymocytes. The impact of this upregulation was reflected in high expression of known target genes (AXIN2, c-MYC, TCF1 and LEF). Especially AXIN2, the universal target gene of WNT pathway, was upregulated at both mRNA and protein levels in ∼40% of the patients. When β-CATENIN gene was silenced by small interfering RNA, the cancer cells showed higher rates of apoptosis. These results demonstrate that abnormal WNT signaling activation occurs in a significant fraction of human T-ALL cases independent of known T-ALL risk factors. We conclude that deregulated WNT signaling is a novel oncogenic event in childhood T-ALL.

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References
1.
Erbilgin Y, Sayitoglu M, Hatirnaz O, Dogru O, Akcay A, Tuysuz G . Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL. Dis Markers. 2010; 28(6):353-60. PMC: 3833232. DOI: 10.3233/DMA-2010-0715. View

2.
Asally M, Yoneda Y . Beta-catenin can act as a nuclear import receptor for its partner transcription factor, lymphocyte enhancer factor-1 (lef-1). Exp Cell Res. 2005; 308(2):357-63. DOI: 10.1016/j.yexcr.2005.05.011. View

3.
Bene M, Castoldi G, Knapp W, Ludwig W, Matutes E, Orfao A . Proposals for the immunological classification of acute leukemias. European Group for the Immunological Characterization of Leukemias (EGIL). Leukemia. 1995; 9(10):1783-6. View

4.
Benhaj K, Akcali K, Ozturk M . Redundant expression of canonical Wnt ligands in human breast cancer cell lines. Oncol Rep. 2006; 15(3):701-7. View

5.
Guo Z, Dose M, Kovalovsky D, Chang R, ONeil J, Look A . Beta-catenin stabilization stalls the transition from double-positive to single-positive stage and predisposes thymocytes to malignant transformation. Blood. 2007; 109(12):5463-72. PMC: 1890819. DOI: 10.1182/blood-2006-11-059071. View