Document Type
Article
Publication Date
5-21-2024
Keywords
Wnt signaling ; Na ; K-ATPase ; Ouabain ; macropinocytosis ; colorectal carcinoma ; multivescular bodies ; Xenopus laevis
Abstract
Recent research has shown that membrane trafficking plays an important role in canonical Wnt signaling through sequestration of the β-catenin destruction complex inside multivesicular bodies (MVBs) and lysosomes. In this study, we introduce Ouabain, an inhibitor of the Na,K-ATPase pump that establishes electric potentials across membranes, as a potent inhibitor of Wnt signaling. We find that Na,K-ATPase levels are elevated in advanced colon carcinoma, that this enzyme is elevated in cancer cells with constitutively activated Wnt pathway and is activated by GSK3 inhibitors that increase macropinocytosis. Ouabain blocks macropinocytosis, which is an essential step in Wnt signaling, probably explaining the strong effects of Ouabain on this pathway. In Xenopus embryos, brief Ouabain treatment at the 32-cell stage, critical for the earliest Wnt signal in development-inhibited brains, could be reversed by treatment with Lithium chloride, a Wnt mimic. Inhibiting membrane trafficking may provide a way of targeting Wnt-driven cancers.
Publisher Attribution
© 2024. Published by The Company of Biologists Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
Recommended Citation
Tejeda-Muñoz, Nydia; Azbazdar, Yagmur; Sosa, Eric A.; Monka, Julia; Wei, Pu-Sheng; Binder, Grace; Mei, Kuo-Ching; Kurmangaliyev, Yerbol Z.; and De Robertis, Edward M., "Na,K-ATPase activity promotes macropinocytosis in colon cancer via Wnt signaling" (2024). Pharmacy Faculty Scholarship. 32.
https://orb.binghamton.edu/pharmacy_fac/32
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Comments
doi.org/10.1242/bio.060269