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cGAS-STING pathway expression as a prognostic tool in NSCLC.
Kristine Raaby Gammelgaard1, Birgitte Sandfeld-Paulsen2, Stine Høvring Godsk1
1Department of Biomedicine, Aarhus University, Aarhus, Denmark.
High expression of the cGAS-STING pathway in lung adenocarcinoma indicates localized disease and is linked to better overall survival (OS). This suggests cGAS, STING, and TBK1 may serve as prognostic biomarkers for localized lung cancer.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Lung adenocarcinoma recurrence poses a significant challenge to patient outcomes.
- Identifying prognostic biomarkers is crucial for risk stratification.
- Immune detection of tumor cells, involving DNA sensing via the cGAS-STING pathway, is vital for cancer clearance.
Purpose of the Study:
- To investigate the expression of the cGAS-STING pathway in tumor tissue and circulating immune cells of lung adenocarcinoma patients.
- To correlate cGAS-STING pathway expression with disease stage and overall survival (OS).
Main Methods:
- Gene expression analysis using droplet digital polymerase chain reaction (ddPCR) in 80 lung adenocarcinoma patients and 45 cancer-free individuals.
- Correlation of expression levels with disease stage.
- Utilizing publicly available gene expression datasets to analyze stage-dependent expression and its relation to OS.
Main Results:
- Differential expression of cGAS-STING pathway components was observed in tumor tissue and peripheral blood mononuclear cells (PBMCs) of cancer patients compared to controls.
- cGAS-STING pathway expression was higher in PBMCs of patients with localized disease (Stage I/II) versus metastatic disease (Stage III/IV).
- Survival analysis revealed superior OS in patients with localized disease and high expression of cGAS, STING, and TBK1.
Conclusions:
- cGAS-STING pathway expression is stage-dependent in lung adenocarcinoma.
- High expression of cGAS, STING, and TBK1 correlates with localized disease and improved OS.
- These genes may represent potential prognostic biomarkers for patients with localized lung adenocarcinoma.
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