Machine learning developed a CD8+ exhausted T cells signature for predicting prognosis, immune infiltration and drug sensitivity in ovarian cancer
- Rujun Chen 1, Yicai Zheng 2, Chen Fei 3, Jun Ye 4, He Fei 5
- Rujun Chen 1, Yicai Zheng 2, Chen Fei 3
- 1Department of Obstetrics and Gynecology, Shanghai Fifth People's Hospital, Fudan University, Shanghai, 200240, China.
- 2Department of Stomatology,Shanghai Fifth People's Hospital, Fudan University, Shanghai, 200240, China.
- 3Shanghai Jiao Tong University, Shanghai, 200240, China.
- 4Department of Obstetrics and Gynecology, Shanghai Fifth People's Hospital, Fudan University, Shanghai, 200240, China. yjun001@aliyun.com.
- 5Department of Obstetrics and Gynecology, Shanghai Fifth People's Hospital, Fudan University, Shanghai, 200240, China. sunshinefh809@aliyun.com.
- 0Department of Obstetrics and Gynecology, Shanghai Fifth People's Hospital, Fudan University, Shanghai, 200240, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study developed a novel prognostic signature for ovarian cancer (OC) using CD8+ exhausted T cells (CD8+ Tex). This signature predicts patient outcomes and response to immunotherapy, offering new insights into OC
Area Of Science
- Oncology
- Immunology
- Bioinformatics
Background
- CD8+ exhausted T cells (CD8+ Tex) are crucial in cancer progression and treatment response.
- Limited understanding exists regarding CD8+ Tex-related genes in ovarian cancer (OC).
Purpose Of The Study
- To construct and validate a CD8+ Tex-related prognostic signature (TRPS) for ovarian cancer.
- To evaluate the TRPS's ability to predict patient prognosis, immune infiltration, and immunotherapy benefits in OC.
Main Methods
- Integrative machine learning using 10 methods on multiple ovarian cancer datasets (TCGA, GSE14764, GSE26193, GSE26712, GSE63885, GSE140082).
- Analysis of immunotherapy benefit indicators: Tumor Immune Dysfunction and Exclusion (TIDE) score, immunophenoscore (IPS), TMB score, and tumor escape score.
- Validation of TRPS performance against clinical factors and existing signatures using C-index.
Main Results
- A TRPS developed by Enet (alpha=0.3) effectively predicted OC patient outcomes as an independent risk factor.
- Low TRPS scores correlated with increased CD8+ T cells, B cells, M1 macrophages, NK cells, and better immunotherapy response indicators (higher IPS, TMB; lower TIDE, tumor escape).
- High TRPS scores were associated with activated cancer hallmarks like angiogenesis, EMT, hypoxia, glycolysis, and notch signaling.
Conclusions
- A novel TRPS for ovarian cancer was successfully constructed.
- The TRPS serves as a valuable indicator for predicting prognosis, immune infiltration, and immunotherapy response in OC patients.
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