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Updated: Jan 7, 2026

An Enrichment Method for Small Extracellular Vesicles Derived from Liver Cancer Tissue
Published on: February 3, 2023
Ribosomal Protein RPL29 Promotes Hepatocellular Carcinoma Progression Through Regulation the Expression of Exosome
1Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Background:
There are notable challenges in the development of effective therapeutic interventions for primary liver cancer (PLC). The role of ribosomal protein (RP) RPL29 in cancer has been rarely reported and the underlying mechanisms of RPL29 in the progression of Hepatocellular carcinoma (HCC) remain unclear.
Methods:
In the present study, the expression level and prognostic value of RPL29 in patients with HCC was evaluated by bioinformatics and immunohistochemistry. Moreover, gene expression was suppressed using targeted siRNAs and enhanced through plasmids containing specific gene cDNA sequences. Subsequently, assessments of cell viability and invasive capacity were conducted. Additionally, Western blot analyses and subcutaneous xenograft models in nude mice were utilized to elucidate the potential function of RPL29 in regulating the malignant phenotype of HCC.
Results:
The expression of RPL29 was found to be significantly elevated in HCC tissues. Further investigation demonstrated that RPL29 actively promotes the proliferation and metastatic potential of HCC cells. Moreover, RPL29 was shown to enhance the expression of Exosome Component 4 (EXOSC4), thereby contributing to the progression and metastasis of HCC. Both RPL29 and EXOSC4 were markedly overexpressed in HCC tissues and were associated with poorer overall survival and disease-free survival outcomes. Notably, the overexpression of RPL29 was able to restore cell viability and invasive capabilities in HCC cells in EXOSC4 silenced cells. In addition, we conducted a screening of two small molecule drugs that specifically target EXOSC4.
Conclusion:
The present study demonstrated that RPL29 facilitates HCC progression by regulating the expression of EXOSC4, which provides a novel therapeutic option for patients with HCC.
Insights
Ribosomal protein RPL29 promotes hepatocellular carcinoma (HCC) progression and metastasis by upregulating EXOSC4. Targeting RPL29 or EXOSC4 offers a new therapeutic strategy for primary liver cancer (PLC).
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Primary liver cancer (PLC) presents significant therapeutic challenges.
- The role and mechanisms of ribosomal protein (RP) RPL29 in hepatocellular carcinoma (HCC) progression are largely unknown.
Purpose of the Study:
- To investigate the expression, prognostic value, and functional role of RPL29 in HCC.
- To elucidate the underlying molecular mechanisms of RPL29 in HCC progression and metastasis.
Main Methods:
- Bioinformatics and immunohistochemistry to assess RPL29 expression and prognostic value in HCC.
- Gene manipulation (siRNA, cDNA) to study RPL29's effect on HCC cell viability and invasion.
- Western blot and xenograft models to explore RPL29's function in regulating HCC malignancy.
- Screening of small molecule drugs targeting EXOSC4.
Main Results:
- RPL29 expression is significantly elevated in HCC tissues and correlates with poorer patient survival.
- RPL29 promotes HCC cell proliferation and metastasis, partly by enhancing Exosome Component 4 (EXOSC4) expression.
- Both RPL29 and EXOSC4 are overexpressed in HCC and associated with adverse outcomes.
- RPL29 overexpression can rescue proliferation and invasion in EXOSC4-silenced HCC cells.
Conclusions:
- RPL29 facilitates HCC progression and metastasis by regulating EXOSC4 expression.
- RPL29 and EXOSC4 represent potential therapeutic targets for HCC treatment.
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