Prognostic significance of SASP-related gene signature of radiation therapy in head and neck squamous cell carcinoma.
Min Kyeong LeeSeon Rang WooJoo Kyung NohSoonki MinMoonkyoo KongYoung-Chan LeeSeong-Gyu KoYoung Gyu EunPublished in: Molecular cancer therapeutics (2024)
In this study,we developed and validated the clinical significance of senescence SASP related gene signature and explored its association with radiation therapy (RT) in patients with head and neck squamous cell carcinoma (HNSCC). First, we searched the three published review literature associated with senescence associated secretory phenotype (SASP) and selected all 81 genes to develop SASP related gene signature. Then, 81 SASP related genes were adapted to gene expression dataset from TCGA. HNSCC patients of TCGA were classified into clusters 1 and 2 via unsupervised clustering according to SASP related gene signature. Kaplan-Meier plot survival analysis showed that cluster 1 had a poorer prognosis than cluster 2 in 5-years overall survival and recurrence-free survival. Similarly, cluster 1 showed a worse prognosis than cluster 2 in three validation cohorts. (E-MTAB-8588, FHCRC and KHU). Cox proportional hazards regression observed that the senescence SASP related signature was an independent prognostic factor for HNSCC patients. We also established a nomogram using a relevant clinical parameter and a risk score. Time-dependent receiver operating characteristic (ROC) analysis was carried out to assess the accuracy of the prognostic risk model and nomogram. Senescence SASP related gene signature was associated with the response to RT. Therefore, subsequent, in vitro experiments further validated the association between senescence SASP related gene signature and RT in HNSCC. In conclusion, we developed a senescence SASP related gene signature, which could predict survival of HNSCC patients, and this gene signature provides new clinical evidence for the accurate diagnosis and targeted RT of HNSCC.
Keyphrases
- genome wide
- radiation therapy
- prognostic factors
- end stage renal disease
- copy number
- free survival
- gene expression
- genome wide identification
- endothelial cells
- dna damage
- newly diagnosed
- ejection fraction
- chronic kidney disease
- squamous cell carcinoma
- machine learning
- peritoneal dialysis
- randomized controlled trial
- transcription factor
- single cell