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Blood vessel epicardial substance reduces LRP6 receptor and cytoplasmic β-catenin levels to modulate Wnt signaling and intestinal homeostasis

Title: Blood vessel epicardial substance reduces LRP6 receptor and cytoplasmic β-catenin levels to modulate Wnt signaling and intestinal homeostasis
Authors: Thompson, Joshua J; Short, Sarah P; Parang, Bobak; Brown, Rachel E; Li, Chenxuan; Ng, Victoria H; Saito-Diaz, Kenyi; Choksi, Yash A; Washington, Mary K; Smith, Jesse Joshua; Fingleton, Barbara; Brand, Thomas; Lee, Ethan; Coffey, Robert J; Williams, Christopher S
Contributors: National Institute of Health; Office of Medical Research, Department of Veterans Affairs
Source: Carcinogenesis ; volume 40, issue 9, page 1086-1098 ; ISSN 0143-3334 1460-2180
Publisher Information: Oxford University Press (OUP)
Publication Year: 2019
Description: Blood vessel epicardial substance (BVES, otherwise known as POPDC1) is an integral membrane protein known to regulate tight junction formation and epithelial–mesenchymal transition. BVES is underexpressed in a number of malignancies, including colorectal cancer. BVES loss leads to activation of the Wnt pathway, suggesting that decreased BVES expression functionally contributes to tumorigenesis. However, the mechanism by which BVES modulates Wnt signaling is unknown. Here, we confirm that BVES loss increases β-catenin protein levels, leads to Wnt pathway activation in a ligand-independent fashion and coordinates with Wnt ligand to further increase Wnt signaling. We show that BVES loss increases levels and activation of the Wnt co-receptor, LRP6, in cell lines, murine adenoma tumoroids and human-derived colonoids. We also demonstrate that BVES interacts with LRP6. Finally, murine tumor modeling using a Wnt-driven genetic model and a chemically induced model of colorectal carcinogenesis demonstrate that BVES loss increases tumor multiplicity and dysplasia. Together, these results implicate BVES as an inhibitor of Wnt signaling, provide one of the first examples of a tight junction-associated protein regulating Wnt receptor levels, and expand the number of putative molecular targets for therapeutic intervention in colorectal cancer.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/carcin/bgz007
Availability: https://doi.org/10.1093/carcin/bgz007; http://academic.oup.com/carcin/article-pdf/40/9/1086/37326898/bgz007.pdf
Rights: https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model
Accession Number: edsbas.B3010E67
Database: BASE