A pyroptosis-related lncRNA risk model for the prediction of prognosis and immunotherapy response in head and neck squamous cell carcinoma
- Jingyuan Ren 1,2, Bingrui Yan 1, Xurui Wang 2, Yifei Wang 3, Qiuying Li 1, Yanan Sun 1
- Jingyuan Ren 1,2, Bingrui Yan 1, Xurui Wang 2
- 1Department of Otorhinolaryngology, Head and Neck Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
- 2Department of Head and Neck Surgery, Jilin Cancer Hospital, Changchun, China.
- 3Department of Pathology, Jilin Cancer Hospital, Changchun, China.
- 0Department of Otorhinolaryngology, Head and Neck Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies two pyroptosis subtypes in head and neck squamous cell carcinoma (HNSC) and develops a six long non-coding RNA (lncRNA) risk model. This model predicts patient survival and response to immunotherapy, offering new therapeutic strategies.
Area Of Science
- Oncology
- Molecular Biology
- Immunology
Background
- Pyroptosis is increasingly recognized as a critical factor in cancer progression.
- Understanding pyroptosis-related signatures is crucial for predicting outcomes in head and neck squamous cell carcinoma (HNSC).
Purpose Of The Study
- To investigate the association between pyroptosis signatures and overall survival (OS) in HNSC.
- To develop a pyroptosis-related long non-coding RNA (lncRNA) risk model for prognosis and immunotherapy response prediction in HNSC.
Main Methods
- Utilized Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) datasets for HNSC expression data.
- Performed consensus clustering to identify pyroptosis-related subtypes.
- Constructed a six-lncRNA risk score model using Cox regression analyses and validated with RT-qPCR and IHC.
Main Results
- Identified two distinct pyroptosis-related subtypes (Cluster A and B), with Cluster B showing significantly poorer OS.
- Developed a six-lncRNA risk score model that effectively stratified patients into high- and low-risk groups with differential OS.
- The risk model correlated with immunotherapy response, indicating better outcomes for the low-risk group receiving immune checkpoint blockade (ICB) therapy.
Conclusions
- Pyroptosis signatures play a significant role in HNSC prognosis.
- The developed six-lncRNA risk model is a valuable tool for predicting HNSC patient prognosis and response to ICB therapy.
- Findings emphasize the importance of pyroptosis and lncRNAs in the HNSC tumor microenvironment, suggesting potential for targeted therapies.
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