ZFC3H1 as an Indicator of Poor Prognosis in Hepatocellular Carcinoma: Bioinformatic Analysis and Experimental Verification
- Jiaxin Zhao 1, Cheng Wang 1, Rui Wu 1, Zheyu Fang 2, Rui Dong 1, Jie Zhou 3, Zhenhua Hu 1,3
- Jiaxin Zhao 1, Cheng Wang 1, Rui Wu 1
- 1Department of Hepatobiliary and Pancreatic Surgery, Department of Surgery, Fourth Affiliated Hospital, School of Medicine, Zhejiang University, Yiwu, Zhejiang, 322000, China.
- 2Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325000, China.
- 3Department of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310000, China.
- 0Department of Hepatobiliary and Pancreatic Surgery, Department of Surgery, Fourth Affiliated Hospital, School of Medicine, Zhejiang University, Yiwu, Zhejiang, 322000, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Zinc finger C3H1-type containing (ZFC3H1) is elevated in liver cancer, promoting tumor growth and migration. Targeting ZFC3H1 may improve hepatocellular carcinoma (HCC) prognosis and immunotherapy response.
Area Of Science
- Oncology
- Molecular Biology
- Genetics
Background
- Zinc finger C3H1-type containing (ZFC3H1) protein's role in RNA regulation is known, but its prognostic significance in hepatocellular carcinoma (HCC) remains unclear.
- Limited research exists on the specific impact of ZFC3H1 on HCC development and patient outcomes.
Purpose Of The Study
- To investigate the prognostic value of ZFC3H1 expression in hepatocellular carcinoma (HCC).
- To explore the functional role of ZFC3H1 in HCC cell proliferation, migration, and the tumor microenvironment.
Main Methods
- Analysis of ZFC3H1 expression in HCC using transcriptomics, immunohistochemistry, and qPCR.
- Functional assays (proliferation, migration, cell cycle) and bioinformatic analyses (GO, KEGG, ESTIMATE) were performed.
- Correlation of ZFC3H1 expression with patient prognosis, tumor mutational burden (TMB), and immunotherapy response was assessed.
Main Results
- ZFC3H1 is significantly upregulated in HCC and correlates with advanced tumor progression.
- High ZFC3H1 expression serves as a negative prognostic factor for HCC patients.
- ZFC3H1 influences the tumor microenvironment, potentially reducing immune infiltration and increasing TMB, impacting immunotherapy efficacy and sorafenib response.
Conclusions
- ZFC3H1 promotes HCC cell proliferation and migration, negatively affecting patient prognosis.
- ZFC3H1 represents a potential therapeutic target and a valuable biomarker for hepatocellular carcinoma.
- Modulating ZFC3H1 expression could enhance HCC treatment strategies, including immunotherapy.
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