Title: |
The Relationship between LRP6 and Wnt/β-Catenin Pathway in Colorectal and Esophageal Cancer |
Authors: |
Akemi Shishido, Masaaki Miyo, Kazuki Oishi, Natsumi Nishiyama, Meiqiao Wu, Hiroyuki Yamamoto, Shihori Kouda, Xin Wu, Satoshi Shibata, Yuhki Yokoyama, Hirofumi Yamamoto |
Source: |
Life, Vol 13, Iss 3, p 615 (2023) |
Publisher Information: |
MDPI AG, 2023. |
Publication Year: |
2023 |
Collection: |
LCC:Science |
Subject Terms: |
LRP6, colorectal cancer, Wnt signaling, esophageal squamous cell carcinoma, Science |
More Details: |
High expression of low-density lipoprotein receptor-related protein 6 (LRP6), a key component of the Wnt/β-catenin signaling pathway, is reported to be associated with malignant potential in some solid tumors including breast cancer and hepatocellular carcinoma. Few reports, however, have examined its function and clinical significance in colorectal cancers (CRC) demonstrating constitutive activation of Wnt signaling. Here, we compared the expression level and function of LRP6 in CRC with that of esophageal squamous cell carcinoma (ESCC) bearing few Wnt/β-catenin pathway mutations. On immunohistochemical staining, high LRP6 expression was noted in three of 68 cases (4.4%), and high β-catenin in 38 of 67 cases (56.7%) of CRC. High LRP6 expression was found in 21 of 82 cases (25.6%), and high β-catenin expression in 29 of 73 cases (39.7%) of ESCC. In our in vitro studies, LRP6 knockdown hardly changed Wnt signaling activity in CRC cell lines with mutations in Wnt signaling downstream genes. In contrast, in ESCC cell lines without Wnt signaling-related mutations, LRP6 knockdown significantly decreased Wnt signaling activity. LRP6 function may depend on constitutive activation of Wnt signaling. |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
2075-1729 |
Relation: |
https://www.mdpi.com/2075-1729/13/3/615; https://doaj.org/toc/2075-1729 |
DOI: |
10.3390/life13030615 |
Access URL: |
https://doaj.org/article/3985c2aa75cf4405be731e9b46d840d8 |
Accession Number: |
edsdoj.3985c2aa75cf4405be731e9b46d840d8 |
Database: |
Directory of Open Access Journals |
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