Identification of the pyroptosis‑related prognostic gene signature and the associated regulation axis in lung adenocarcinoma

• Published in: Cell death discovery 2021-06, Vol.7 (1), p.161-161, Article 161
• Main Authors: Lin, Wanli, Chen, Ying, Wu, Bomeng, chen, Ying, Li, Zuwei
• Format: Article
• Language: English
• Subjects: 631/67/1612/1350; 692/53/2422; Adenocarcinoma; Apoptosis; Biochemistry; Bioinformatics; Biomedical and Life Sciences; Cell Biology; Cell Cycle Analysis; Cell proliferation; Correlation analysis; Genes; Genetic diversity; Infiltration; KCNQ1OT1 protein; Life Sciences; Lung cancer; Medical prognosis; Metastases; Microsatellite instability; Mutation; Nod1 protein; Potassium channels (voltage-gated); Prognosis; Pyroptosis; Signal transduction; Stem Cells; Toll-like receptors; Tumors
• ISSN: 2058-7716; 2058-7716
• DOI: 10.1038/s41420-021-00557-2

Lung adenocarcinoma (LUAD) remains the most common deadly disease and has a poor prognosis. Pyroptosis could regulate tumour cell proliferation, invasion, and metastasis, thereby affecting the prognosis of cancer patients. However, the role of pyroptosis-related genes (PRGs) in LUAD remains unclear. In our study, comprehensive bioinformatics analysis was performed to construct a prognostic gene model and ceRNA network. The correlations between PRGs and tumour-immune infiltration, tumour mutation burden, and microsatellite instability were evaluated using Pearson’s correlation analysis. A total of 23 PRGs were upregulated or downregulated in LUAD. The genetic mutation variation landscape of PRG in LUAD was also summarised. Functional enrichment analysis revealed that these 33 PRGs were mainly involved in pyroptosis, the NOD-like receptor signalling pathway, and the Toll-like receptor signalling pathway. Prognosis analysis indicated a poor survival rate in LUAD patients with low expression of NLRP7, NLRP1, NLRP2, and NOD1 and high CASP6 expression. A prognostic PRG model constructed using the above five prognostic genes could predict the overall survival of LUAD patients with medium-to-high accuracy. Significant correlation was observed between prognostic PRGs and immune-cell infiltration, tumour mutation burden, and microsatellite instability. A ceRNA network was constructed to identify a lncRNA KCNQ1OT1/miR-335-5p/NLRP1/NLRP7 regulatory axis in LUAD. In conclusion, we performed a comprehensive bioinformatics analysis and identified a prognostic PRG signature containing five genes (NLRP7, NLRP1, NLRP2, NOD1, and CASP6) for LUAD patients. Our results also identified a lncRNA KCNQ1OT1/miR-335-5p/NLRP1/NLRP7 regulatory axis, which may also play an important role in the progression of LUAD. Further study needs to be conducted to verify this result.