SOX11 as a potential prognostic biomarker in hepatocellular carcinoma linked to immune infiltration and ferroptosis
- Hongyu Chen 1, Qiangguo Ao 1, Yueling Wang 2, Yue Qian 3, Qingli Cheng 1, Wei Zhang 3,4
- Hongyu Chen 1, Qiangguo Ao 1, Yueling Wang 2
- 1Department of Nephrology, the Second Medical Center of PLA General Hospital, National Clinical Research Center for Geriatric Diseases, Beijing 100853, China.
- 2Clinical Laboratory, the First Affiliated Hospital of Henan University, Kaifeng 475000, China.
- 3Cell Biology Department, Wuxi School of Medicine, Jiangnan University, Wuxi 214122, China.
- 4Department of Pathogen Biology, Guizhou Nursing Vocational College, Guiyang 550000, China.
- 0Department of Nephrology, the Second Medical Center of PLA General Hospital, National Clinical Research Center for Geriatric Diseases, Beijing 100853, China.
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September 9, 2024
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View abstract on PubMed
Summary
This summary is machine-generated.SOX11 is elevated in hepatocellular carcinoma (HCC) and correlates with poor prognosis. Targeting SOX11 may offer a new therapeutic strategy for HCC patients.
Area Of Science
- Oncology
- Genetics
- Bioinformatics
Background
- SOX11 is implicated in various cancers, including hepatocellular carcinoma (HCC).
- The precise role of SOX11 in HCC tumorigenesis remains unclear.
- Understanding SOX11's function is crucial for developing targeted therapies.
Purpose Of The Study
- To comprehensively investigate the role of SOX11 in HCC tumorgenesis.
- To analyze SOX11 expression and its association with clinical features and patient outcomes in HCC.
- To explore SOX11 as a potential diagnostic and prognostic biomarker for HCC.
Main Methods
- Bioinformatics analysis of TCGA and GEO datasets for SOX11 expression.
- Immunohistochemistry validation of SOX11 protein levels.
- Functional enrichment analysis using Metascape and LinkedOmics.
- Assessment of associations with immune infiltration, ferroptosis, and immune checkpoints.
- In vitro studies on HCC cell lines (HepG2, HuH7) to evaluate proliferation and migration.
Main Results
- SOX11 expression was significantly upregulated in HCC tumors compared to normal liver tissue.
- SOX11 levels correlated with advanced HCC stage, higher histologic grade, and tumor status.
- SOX11 independently predicted both overall and disease-specific survival in HCC patients.
- SOX11 expression was associated with immune infiltration, ferroptosis, and immune checkpoint genes.
- Reduced SOX11 expression in vitro led to decreased HCC cell proliferation and migration.
Conclusions
- SOX11 serves as a potential diagnostic biomarker for HCC.
- SOX11 is a significant prognostic indicator for HCC patient survival.
- SOX11 represents a potential therapeutic target for HCC treatment.
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