Abstract
Background: The Wnt/Wingless signalling pathway plays an important role in both embryonic development and tumorigenesis. β-Catenin and Axin are positive and negative effectors of the Wnt signalling pathway, respectively. Results: We found that Axin interacts with β-catenin and glycogen synthase kinase-3β (GSK-3β). Furthermore, the regulation of the G-protein signalling (RGS) domain of Axin is associated with the colorectal tumour suppressor adenomatous polyposis coli (APC). Overexpression of Axin in the human colorectal cancer cell line SW480 induced a drastic reduction in the level of β-catenin. Interaction with β-catenin and GSK-3β was required for the Axin-mediated β-catenin reduction. Conclusion: Axin interacts with β- catenin, GSK-3β and APC, and negatively regulates the Wnt signalling pathways, presumably by regulating the level of β-catenin.
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CITATION STYLE
Nakamura, T., Hamada, F., Ishidate, T., Anai, K. I., Kawahara, K., Toyoshima, K., & Akiyama, T. (1998). Axin, an inhibitor of the Wnt signalling pathway, interacts with β- catenin, GSK-3β and APC and reduces the β-catenin level. Genes to Cells, 3(6), 395–403. https://doi.org/10.1046/j.1365-2443.1998.00198.x
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