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Role of the Wnt Pathway in Thyroid Cancer

Overview
Specialty Endocrinology
Date 2012 May 31
PMID 22645520
Citations 63
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Abstract

Aberrant activation of Wnt signaling is involved in the development of several epithelial tumors. Wnt signaling includes two major types of pathways: (i) the canonical or Wnt/β-catenin pathway; and (ii) the non-canonical pathways, which do not involve β-catenin stabilization. Among these pathways, the Wnt/β-catenin pathway has received most attention during the past years for its critical role in cancer. A number of publications emphasize the role of the Wnt/β-catenin pathway in thyroid cancer. This pathway plays a crucial role in development and epithelial renewal, and components such as β-catenin and Axin are often mutated in thyroid cancer. Although it is accepted that altered Wnt signaling is a late event in thyroid cell transformation that affects anaplastic thyroid tumors, recent data suggest that it is also altered in papillary thyroid carcinoma (PTC) with RET/PTC mutations. Therefore, the purpose of this review is to summarize the main relevant data of Wnt signaling in thyroid cancer, with special emphasis on the Wnt/β-catenin pathway.

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References
1.
Hulsken J, Birchmeier W, Behrens J . E-cadherin and APC compete for the interaction with beta-catenin and the cytoskeleton. J Cell Biol. 1994; 127(6 Pt 2):2061-9. PMC: 2120290. DOI: 10.1083/jcb.127.6.2061. View

2.
Kroll T, Sarraf P, Pecciarini L, Chen C, Mueller E, Spiegelman B . PAX8-PPARgamma1 fusion oncogene in human thyroid carcinoma [corrected]. Science. 2000; 289(5483):1357-60. DOI: 10.1126/science.289.5483.1357. View

3.
Cetta F, Chiappetta G, Melillo R, Petracci M, Montalto G, Santoro M . The ret/ptc1 oncogene is activated in familial adenomatous polyposis-associated thyroid papillary carcinomas. J Clin Endocrinol Metab. 1998; 83(3):1003-6. DOI: 10.1210/jcem.83.3.4614. View

4.
Castellone M, De Falco V, Magendra Rao D, Bellelli R, Muthu M, Basolo F . The beta-catenin axis integrates multiple signals downstream from RET/papillary thyroid carcinoma leading to cell proliferation. Cancer Res. 2009; 69(5):1867-76. PMC: 2746012. DOI: 10.1158/0008-5472.CAN-08-1982. View

5.
Rubinfeld B, Albert I, Porfiri E, Fiol C, MUNEMITSU S, Polakis P . Binding of GSK3beta to the APC-beta-catenin complex and regulation of complex assembly. Science. 1996; 272(5264):1023-6. DOI: 10.1126/science.272.5264.1023. View