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Human Neuralized is a novel tumour suppressor targeting Wnt/β-catenin signalling in colon cancer

Authors
Yi, Joo MiKang, Tae-HongHan, Yu KyeongPark, Ha YoungYang, Ju HwanBae, Jin-HanSuh, Jung-SooKim, Tae-JinKim, Joong-GookCui, Yan-HongSuzuki, HiromuKumegawa, KoheiKim, Sung JooZhao, YiPark, In JaHong, Seung-MoChung, Joon-YongLee, Su-Jae
Issue Date
Jan-2023
Publisher
John Wiley and Sons Inc
Keywords
epigenetic alterations; Neuralized; tumour suppressor; ubiquitin E3 ligase; Wnt/β-catenin pathway
Citation
EMBO Reports, v.24, no.8
Indexed
SCIE
SCOPUS
Journal Title
EMBO Reports
Volume
24
Number
8
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/67743
DOI
10.15252/embr.202256335
ISSN
1469-221X
1469-3178
Abstract
While there is growing evidence that many epigenetically silenced genes in cancer are tumour suppressor candidates, their significance in cancer biology remains unclear. Here, we identify human Neuralized (NEURL), which acts as a novel tumour suppressor targeting oncogenic Wnt/β-catenin signalling in human cancers. The expression of NEURL is epigenetically regulated and markedly suppressed in human colorectal cancer. We, therefore, considered NEURL to be a bona fide tumour suppressor in colorectal cancer and demonstrate that this tumour suppressive function depends on NEURL-mediated oncogenic β-catenin degradation. We find that NEURL acts as an E3 ubiquitin ligase, interacting directly with oncogenic β-catenin, and reducing its cytoplasmic levels in a GSK3β- and β-TrCP-independent manner, indicating that NEURL-β-catenin interactions can lead to a disruption of the canonical Wnt/β-catenin pathway. This study suggests that NEURL is a therapeutic target against human cancers and that it acts by regulating oncogenic Wnt/β-catenin signalling. © 2023 The Authors.
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