Identification of prognostic genes associated with phase separation in lung adenocarcinoma and construction of prognostic models
- Hanlin Wang 1, Qi Zhang 1, Yiwei Liu 1, Jiaxin Tang 2, Xiu Chen 1, Renquan Zhang 3
- Hanlin Wang 1, Qi Zhang 1, Yiwei Liu 1
- 1Department of Thoracic Surgery, The First Affiliated Hospital of Anhui Medical University, Jixi Road, Shushan District, Hefei City, 230022, Anhui, China.
- 2Department of Dermatology, Anhui Provincial Hospital, Hefei, 230001, China.
- 3Department of Thoracic Surgery, The First Affiliated Hospital of Anhui Medical University, Jixi Road, Shushan District, Hefei City, 230022, Anhui, China. zrqahmu@163.com.
- 0Department of Thoracic Surgery, The First Affiliated Hospital of Anhui Medical University, Jixi Road, Shushan District, Hefei City, 230022, Anhui, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies seven prognostic genes related to liquid-liquid phase separation in lung adenocarcinoma (LUAD). The developed risk model accurately predicts patient survival, aiding personalized LUAD treatment strategies.
Area Of Science
- Oncology
- Genomics
- Bioinformatics
Background
- Lung adenocarcinoma (LUAD) has a poor prognosis despite being a common cancer subtype.
- Liquid-liquid phase separation-related genes (LRGs) show promise in predicting prognosis for certain tumors.
- Identifying LRGs for LUAD prognosis is crucial for clinical applications.
Purpose Of The Study
- To identify and validate LRGs that can predict prognosis in LUAD.
- To develop a prognostic risk model for LUAD patients.
- To explore the relationship between prognostic genes, immune characteristics, and cell types in LUAD.
Main Methods
- Differential expression analysis and dataset intersection to identify DE-LRGs.
- Lasso regression and multivariate Cox regression to build a prognostic risk model.
- Nomogram construction, immune profiling, and single-cell RNA sequencing (scRNA-seq) analysis.
Main Results
- 389 DE-LRGs were identified, and 7 prognostic genes were selected for the risk model.
- The high-risk group showed significantly lower survival rates; the nomogram demonstrated high predictive accuracy.
- Distinct immune profiles and drug sensitivities were observed between high- and low-risk groups. GRIA1 and BCAN were highly expressed in fibroblasts and mast cells, respectively.
Conclusions
- A 7-gene prognostic model accurately predicts LUAD patient survival.
- The model offers valuable insights for improving LUAD prognosis and guiding personalized treatment.
- The study highlights the role of specific LRGs in LUAD progression and immune microenvironment.
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