Comprehensive Analysis of a Six-Gene Signature Predicting Survival and Immune Infiltration of Liposarcoma Patients and Deciphering Its Therapeutic Significance
- Jiayang Han 1,2, Binbin Zhao 1,2, Xu Han 1,2, Tiantian Sun 1,2, Man Yue 1,2, Mengwen Hou 1,2, Jialin Wu 1,2, Mengjie Tu 1,2, Yang An 1,2
- Jiayang Han 1,2, Binbin Zhao 1,2, Xu Han 1,2
- 1Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Henan University, Kaifeng 475004, China.
- 2Henan Provincial Engineering Center for Tumor Molecular Medicine, Kaifeng Key Laboratory of Cell Signal Transduction, Henan University, Kaifeng 475004, China.
- 0Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Henan University, Kaifeng 475004, China.
Related Experiment Videos
Contact us if these videos are not relevant.
Contact us if these videos are not relevant.
View abstract on PubMed
Summary
This summary is machine-generated.A new six-gene signature predicts distant recurrence-free survival in liposarcoma (LPS) patients. This model aids in assessing LPS prognosis and developing targeted therapeutic strategies for improved patient outcomes.
Area Of Science
- Oncology
- Genomics
- Bioinformatics
Background
- Liposarcoma (LPS) is a prevalent soft tissue sarcoma with a poor prognosis due to high rates of metastasis and recurrence.
- Accurate prognosis evaluation is crucial for improving clinical treatment strategies in LPS patients.
Purpose Of The Study
- To develop a robust risk prediction model for evaluating the prognosis of LPS patients.
- To identify key genes associated with distant recurrence-free survival (DRFS) in LPS.
Main Methods
- Differential gene expression analysis of GEO datasets to identify DEGs.
- Univariate and Lasso Cox regression for DRFS-associated DEGs and signature development.
- Kaplan-Meier survival, ROC curve, GSEA, and immune infiltration analyses for model validation and mechanism exploration.
Main Results
- A prognostic six-gene signature was developed to predict DRFS in LPS patients, demonstrating higher precision in aggressive subtypes.
- A clinical nomogram was established based on the risk model.
- GSEA revealed enrichment in cell cycle pathways for the high-risk group, and immune cell abundance differed between risk groups.
Conclusions
- The developed six-gene signature is a valuable tool for LPS risk assessment.
- The signature correlates with cell cycle pathways and therapeutic targets, offering insights for improved treatment strategies and patient prognosis.
Related Experiment Videos
Contact us if these videos are not relevant.
Contact us if these videos are not relevant.

