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Identification of a Cancer Stem Cell-Related Gene Signature in Hepatocellular Carcinoma Based on Single-Cell RNA-Seq
Jing Wu1, Xu Liu1, Sheng Huang1
1Medical School, Hubei Minzu University, Enshi 445000, China.
This study identifies nine cancer stem cell biomarkers (BCSCs) to predict liver hepatocellular carcinoma (LIHC) patient outcomes. High-risk LIHC patients show poorer survival, suggesting a new model for personalized cancer therapy.
Area of Science:
- Oncology
- Genomics
- Immunology
Background:
- Cancer stem cells (CSCs) drive liver hepatocellular carcinoma (LIHC) progression, therapeutic resistance, and recurrence.
- Identifying prognostic biomarkers for LIHC is crucial for developing effective treatments.
Purpose of the Study:
- To explore the prognostic significance of cancer stem cell biomarkers (BCSCs) in LIHC.
- To develop a prognostic risk model for LIHC based on BCSCs.
Main Methods:
- Integrated analysis of TCGA, ICGA, and GEO (GSE156625) datasets including bulk and single-cell RNA sequencing.
- Development and validation of a nine-BCSC prognostic risk model.
- Characterization of immune cell composition and gene expression in the tumor microenvironment (TME).
Main Results:
- A prognostic risk model based on nine BCSCs (ADM, CCL5, CD274, DLGAP5, HOXD9, IGF1, S100A9, SOCS2, TNFRSF11B) was developed.
- High-risk LIHC patients exhibited significantly shorter overall survival.
- Distinct immune cell compositions and gene expression patterns were observed between high- and low-risk groups, suggesting immune evasion independent of PD-L1.
Conclusions:
- The developed BCSC-based risk model effectively predicts LIHC patient prognosis.
- Liver cancer progression may involve immune evasion mechanisms not solely dependent on PD-L1.
- The low-risk BCSC group shows potential sensitivity to various therapies, paving the way for personalized LIHC treatment strategies.
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