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Updated: Jun 27, 2025

Phosphopeptide Enrichment Coupled with Label-free Quantitative Mass Spectrometry to Investigate the Phosphoproteome in Prostate Cancer
Published on: August 2, 2018
Sphingolipids in prostate cancer prognosis: integrating single-cell and bulk sequencing
Shan Zhou1, Li Sun1, Fei Mao2,3
1Department of Ultrasound, The Affiliated Huaian No. 1 People’s Hospital of Nanjing Medical University, Huaian City 223300, People’s Republic of China.
This study identifies key genes in prostate cancer, developing a prognostic model for sphingolipid metabolism to stratify patient risk and improve outcomes. The model aids in understanding the tumor microenvironment and guiding treatment strategies.
Area of Science:
- Oncology
- Genomics
- Bioinformatics
Background:
- Stratifying patient risk is crucial for prostate cancer management.
- Understanding the tumor microenvironment is essential for advancing prostate cancer research.
Purpose of the Study:
- To identify key genes in prostate cancer pathogenesis.
- To develop a prognostic model for risk stratification.
- To explore the role of sphingolipid metabolism in prostate cancer.
Main Methods:
- Integrative analysis of single-cell and bulk transcriptome data.
- Weighted gene coexpression network analysis (WGCNA) for gene module identification.
- Prognostic model development using Cox and LASSO regression.
Main Results:
- A five-gene prognostic model (SRSR) for sphingolipid metabolism was constructed.
- The SRSR model effectively stratified patients into high- and low-risk groups.
- Distinct differences in the immune microenvironment were observed between risk groups.
Conclusions:
- The SRSR model shows promise for improving prostate cancer risk stratification and patient outcomes.
- Sphingolipid metabolism plays a significant role in prostate cancer diagnosis and treatment.
- Further research can leverage this model for clinical applications.
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