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Updated: Jul 31, 2025

Author Spotlight: Investigating Immune Cell Dynamics in the Tumor Microenvironment — Challenges and Innovations in Cancer Prognosis
Published on: April 12, 2024
EPRS1 correlates with malignant progression in hepatocellular carcinoma
Chen Yang1,2,3, Xiaofeng Yang1,2, Chenghao Liu1,2
1NHC Key Laboratory of Prevention and Treatment of Central Asia High Incidence Diseases, the First Affiliated Hospital, Shihezi University School of Medicine, Shihezi, Xinjiang, China.
Glutamyl-prolyl-tRNA synthetase 1 (EPRS1) promotes liver cancer growth and spread. Upregulated EPRS1 expression in hepatocellular carcinoma (HCC) is linked to poor survival, suggesting EPRS1 as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Glutamyl-prolyl-tRNA synthetase 1 (EPRS1) is implicated in cancer development.
- Its specific role in hepatocellular carcinoma (HCC) requires further investigation.
Purpose of the Study:
- To elucidate the carcinogenic function, underlying mechanisms, and clinical relevance of EPRS1 in human HCC.
- To assess EPRS1 as a potential therapeutic target for HCC.
Main Methods:
- Utilized TCGA and GEO databases for expression and prognostic analysis.
- Performed cell-based assays (CCK-8, Transwell, hepatosphere) to evaluate EPRS1 function.
- Employed immunohistochemistry, proteomics, cBioportal, and MEXEPRSS for mechanistic and variation analysis.
Main Results:
- EPRS1 mRNA and protein levels were significantly elevated in HCC.
- Higher EPRS1 expression correlated with reduced patient survival.
- EPRS1 promoted HCC cell proliferation, stemness, and migration by upregulating LAMC1 and CCNB1.
Conclusions:
- Enhanced EPRS1 expression drives HCC development by increasing oncogene expression in the tumor microenvironment.
- EPRS1 presents a promising therapeutic target for HCC treatment.
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