CPEB3-mediated MTDH mRNA translational suppression restrains hepatocellular carcinoma progression
He Zhang1, Chendan Zou1, Zini Qiu1
1Department of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, Heilongjiang, 150081, China.
Abstract:
Cytoplasmic polyadenylation element-binding protein 3 (CPEB3) is a sequence-specific RNA-binding protein. We had reported that CPEB3 is involved in hepatocellular carcinoma (HCC) progression. However, the underlying mechanisms of CPEB3 in HCC remain unclear. In this study, we firstly performed RNA immunoprecipitation to uncover the transcriptome-wide CPEB3-bound mRNAs (CPEB3 binder) in HCC. Bioinformatic analysis indicates that CPEB3 binders are closely related to cancer progression, especially HCC metastasis. Further studies confirmed that metadherin (MTDH) is a direct target of CPEB3. CPEB3 can suppress the translation of MTDH mRNA in vivo and in vitro. Besides, luciferase assay demonstrated that CPEB3 interacted with 3'-untranslated region of MTDH mRNA and inhibited its translation. Subsequently, CPEB3 inhibited the epithelial-mesenchymal transition and metastasis of HCC cells through post-transcriptional regulation of MTDH. In addition, cpeb3 knockout mice are more susceptible to carcinogen-induced hepatocarcinogenesis and subsequent lung metastasis. Our results also indicated that CPEB3 was a good prognosis marker, which is downregulated in HCC tissue. In conclusion, our results demonstrated that CPEB3 played an important role in HCC progression and targeting CPEB3-mediated mRNA translation might be a favorable therapeutic approach.
Insights
Cytoplasmic polyadenylation element-binding protein 3 (CPEB3) suppresses hepatocellular carcinoma (HCC) metastasis by inhibiting metadherin (MTDH) translation. Downregulated CPEB3 correlates with poor prognosis in HCC, suggesting therapeutic potential.
Area of Science:
- Molecular Biology
- Oncology
- Gene Regulation
Background:
- Cytoplasmic polyadenylation element-binding protein 3 (CPEB3) is implicated in hepatocellular carcinoma (HCC) progression.
- The precise mechanisms of CPEB3's role in HCC remain largely undefined.
Purpose of the Study:
- To elucidate the molecular mechanisms underlying CPEB3's function in HCC.
- To identify direct targets of CPEB3 and their role in HCC metastasis.
Main Methods:
- RNA immunoprecipitation to identify CPEB3-bound mRNAs in HCC.
- Bioinformatic analysis of CPEB3 targets.
- Luciferase assays to confirm direct interaction and translational inhibition.
- In vivo and in vitro studies using HCC cell lines and knockout mice.
Main Results:
- CPEB3 directly binds and suppresses the translation of metadherin (MTDH) mRNA.
- CPEB3 inhibits epithelial-mesenchymal transition and metastasis in HCC cells via MTDH regulation.
- CPEB3 knockout mice exhibit increased susceptibility to HCC development and metastasis.
- CPEB3 is downregulated in HCC tissues and serves as a favorable prognostic marker.
Conclusions:
- CPEB3 plays a critical role in suppressing HCC progression and metastasis.
- Targeting CPEB3-mediated mRNA translation presents a potential therapeutic strategy for HCC.
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