Background: Stabilization of RAS is a key event for the hyper-activation of Wnt/β-catenin signaling and activation of cancer stem cell (CSC) in colorectal cancer (CRC). WD Repeat protein 76 (WDR76) mediates the polyubiquitination-dependent degradation of RAS in hepatocellular carcinoma (HCC). We investigated whether WDR76 destabilizes RAS and acts as a tumor suppressor inhibiting CSC activation in CRC. Methods: We generated mice with deletion of Wdr76 (Wdr76 -/- ) and crosses of Wdr76 -/- with Apc Min/+ (Wdr76 -/- ; Apc Min/+ ) and compared them with wildtype mice (Wdr76 +/+ ) and Apc Min/+ mice (Wdr76 +/+ ; Apc Min/+ ), respectively. Intestinal crypt lengthening, tumorigenesis and CSC activation were analyzed by histology, immunohistochemistry, and immunoblotting. CRC cell line was engineered to stably express or knockdown WDR76 or control vector and was analyzed after spheroid culture. Results: Wdr76 -/- mice, with increased Ras level, displayed crypt elongation and hyper-proliferation. Wdr76 -/- ; Apc Min/+ mice developed more tumors with bigger sizes than Apc Min/+ mice and their tumors showed increased proliferation and CSC activation with elevated RAS and β-catenin levels. In CRC cells, overexpression or knockdown of WDR76 decreased or increased the numbers and sizes of CRC spheroids with inhibition or activation of CSC markers, respectively. In human CRC, lower level of WDR76 was associated with poor patient survival. Conclusions: In analyses of mice with deletion of Wdr76 and CRC spheroids, we found that RAS stability plays important roles in tumorigenesis by affecting proliferation and CSC activation. Our results suggest that destabilization of RAS by WDR76 is a potential strategy for targeting malignant CRC involving CSC activation. Graphic abstract: [Figure not available: See fulltext.]
|Journal||Cell Communication and Signaling|
|Publication status||Published - 2019 Jul 30|
Bibliographical noteFunding Information:
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean Government (MSIP) (grants 2016R1A5A1004694, 2019R1A2C3002751).
© 2019 The Author(s).
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Cell Biology