Integrated Multiomics Reveals Silencing of has_circ_0006646 Promotes TRIM21‐Mediated NCL Ubiquitination to Inhibit Hepatocellular Carcinoma Metastasis

Author:

Hu Xin123,Chen Guanrong4,Huang Yingchen4,Cheng Qiyang5,Zhuo Jianyong26,Su Renyi12,He Chiyu17,Wu Yichao12,Liu Zhikun26,Yang Beng8,Wang Shuai26,Meng Lijun26,Zheng Shusen378,Lu Di26,Wei Qiang26,Yang Jiayin9,Wei Xuyong26,Chen Ronggao38,Xu Xiao123ORCID

Affiliation:

1. Zhejiang University School of Medicine Hangzhou 310058 China

2. Key Laboratory of Integrated Oncology and Intelligent Medicine of Zhejiang Province Hangzhou 310006 China

3. NHC Key Laboratory of Combined Multi‐organ Transplantation Hangzhou 310003 China

4. The Fourth School of Clinical Medicine Zhejiang Chinese Medical University Hangzhou 310053 China

5. Department of Hepatobiliary Surgery Beijing Chaoyang Hospital affiliated to Capital Medical University Beijing 100020 China

6. Department of Hepatobiliary and Pancreatic Surgery Affiliated Hangzhou First People's Hospital Zhejiang University School of Medicine Hangzhou 310006 China

7. Department of Hepatobiliary and Pancreatic Surgery Shulan (Hangzhou) Hospital Hangzhou 310022 China

8. Department of Hepatobiliary and Pancreatic Surgery The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou 310006 China

9. Department of Liver Surgery Liver Transplantation Center West China Hospital of Sichuan University Chengdu 332001 China

Abstract

AbstractRecent studies suggest that circular RNA (circRNA)‐mediated post‐translational modification of RNA‐binding proteins (RBP) plays a pivotal role in metastasis of hepatocellular carcinoma (HCC). However, the specific mechanism and potential clinical therapeutic significance remain vague. This study attempts to profile the regulatory networks of circRNA and RBP using a multi‐omics approach. Has_circ_0006646 (circ0006646) is an unreported circRNA in HCC and is associated with a poor prognosis. Silencing of circ0006646 significantly hinders metastasis in vivo. Mechanistically, circ0006646 prevents the interaction between nucleolin (NCL) and the E3 ligase tripartite motif‐containing 21 to reduce the proteasome‐mediated degradation of NCL via K48‐linked polyubiquitylation. Furthermore, the change of NCL expression is proven to affect the phosphorylation levels of multiple proteins and inhibit p53 translation. Moreover, patient‐derived tumor xenograft and lentivirus injection, which is conducted to simulate clinical treatment confirmed the potential therapeutic value. Overall, this study describes the integrated multi‐omics landscape of circRNA‐mediated NCL ubiquitination degradation in HCC metastasis and provides a novel therapeutic target.

Funder

National Key Research and Development Program of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

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