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Original research
Reticulon 3-mediated Chk2/p53 activation suppresses hepatocellular carcinogenesis and is blocked by hepatitis B virus
  1. Shushu Song1,
  2. Yinghong Shi2,
  3. Weicheng Wu1,
  4. Hao Wu1,
  5. Lei Chang3,
  6. Peike Peng1,
  7. Lei Zhang4,
  8. Jia Fan2,
  9. Jianxin Gu1,
  10. Yuanyuan Ruan1
  1. 1 Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai, China
  2. 2 Department of Liver Surgery, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China
  3. 3 State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing, China
  4. 4 Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China
  1. Correspondence to Dr Yuanyuan Ruan, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China; ryyfdu{at}126.com

Abstract

Objective Dysfunction of endoplasmic reticulum (ER) proteins is closely related to homeostasis disturbance and malignant transformation of hepatocellular carcinoma (HCC). Reticulons (RTN) are a family of ER-resident proteins critical for maintaining ER function. Nevertheless, the precise roles of RTN in HCC remain largely unclear. The aim of the study is to examine the effect of reticulon family member RTN3 on HCC development and explore the underlying mechanisms.

Design Clinical HCC samples were collected to assess the relationship between RTN3 expression and patients’ outcome. HCC cell lines were employed to examine the effects of RTN3 on cellular proliferation, apoptosis and signal transduction in vitro. Nude mice model was used to detect the role of RTN3 in modulating tumour growth in vivo.

Results We found that RTN3 was highly expressed in normal hepatocytes but frequently downregulated in HCC. Low RTN3 expression predicted poor outcome in patients with HCC in TP53 gene mutation and HBV infection status-dependent manner. RTN3 restrained HCC growth and induced apoptosis by activating p53. Mechanism studies indicated that RTN3 facilitated p53 Ser392 phosphorylation via Chk2 and enhanced subsequent p53 nuclear localisation. RTN3 interacted with Chk2, recruited it to ER and promoted its activation in an ER calcium-dependent manner. Nevertheless, the tumour suppressive effects of RTN3 were abrogated in HBV-positive cells. HBV surface antigen competed with Chk2 for RTN3 binding and blocked RTN3-mediated Chk2/p53 activation.

Conclusion The findings suggest that RTN3 functions as a novel suppressor of HCC by activating Chk2/p53 pathway and provide more clues to better understand the oncogenic effects of HBV.

  • hepatoma
  • cell proliferation
  • cell death
  • signal transduction

Data availability statement

All data relevant to the study are available upon reasonable request. Please contact YR (email: ryyfdu@126.com) for any enquiries.

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Data availability statement

All data relevant to the study are available upon reasonable request. Please contact YR (email: ryyfdu@126.com) for any enquiries.

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Footnotes

  • Contributors SS performed all the experiments. SS and YR designed the experiments. PP and LZ collected clinical data and performed the IHC experiments. YS, HW and LC carried out the statistical analysis. SS and YR cowrote the manuscript. JG, YR, JF and WW conceived the project. All authors have approved the final version of the manuscript.

  • Funding This work was supported by grants from the National Key R&D Program of China (2018YFC0910303), the National Natural Science Fund (31630088, 31370808, 82073245, 31770855, 81572317, 81972257, 31500645), the Shanghai Rising-Star Program (17QA1400300) and China Postdoctoral Science Foundation (2018M640344).

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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