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Updated: Oct 18, 2025

Author Spotlight: Flow Cytometric Determination of Pyroptosis in Avian Cells
Published on: May 31, 2024
Role of Cytokines Released During Pyroptosis in Non-Small Cell Lung Cancer
Yuanli Huang1,2, Guanghui Zhang1,2, Qing Zhu1
1Department of Pathology, the First Affiliated Hospital of Bengbu Medical College, Bengbu City, Anhui Province, People's Republic of China.
Purpose:
Pyroptosis is a recently discovered highly inflammatory form of programmed cell death, during which the N-terminus of the cleaved Gasdermin protein family forms pores in the cell membrane, leading to cell disintegration and the release of certain intracellular factors, including caspase3, gasdermin E (GSDME), and high mobility group proteins (HMGB1), which trigger a series of secondary inflammatory reactions. Specifically, caspase3 can lyse GSDME and induce pyrolysis, while HMGB1 is released passively after cell membrane destruction. In this study, the roles of these proteins in lung cancer tissues as well as their clinical significance were investigated.
Patients And Methods:
The expression levels of GSDME, caspase3, and HMGB1 proteins in lung cancer and paracancerous tissues were determined via immunohistochemical staining, and their relationship with the clinical stage, pathological grade, and survival prognosis of the patients was analyzed. Further, CD8+ T cell accumulation in the above-mentioned tissues was also determined, and differences between them with respect to CD8+T cell distribution were also investigated. Furthermore, the relationships between CD8+ T cell abundance and the expression levels of the above-mentioned proteins were determined via statistical analyses.
Results:
Lung cancer and paracancerous tissues showed significantly different GSDME, caspase3, and HMGB1 protein expression levels. GSDME expression level and the presence or absence of lymph node invasion were identified as prognostic indicators of survival in patients with lung cancer. Surprisingly, however, HMGB1, which showed a certain level of correlation with the presence or absence of lymph node metastasis, could not be used as a prognostic indicator of survival.
Conclusion:
GSDME may be an important prognostic indicator of survival in patients with lung cancer. However, the effects of HMGB1 expression level and CD8+ T cell abundance on the prognosis of patients with lung cancer still need further investigation.
Insights
Gasdermin E (GSDME) expression in lung cancer tissues may predict patient survival. High GSDME levels indicate a better prognosis, while High Mobility Group Protein B1 (HMGB1) and CD8+ T cell roles require further study.
Area of Science:
- Oncology
- Cell Biology
- Immunology
Background:
- Pyroptosis is an inflammatory programmed cell death pathway involving Gasdermin proteins.
- Cleaved Gasdermin E (GSDME) forms pores, releasing inflammatory factors like High Mobility Group Protein B1 (HMGB1).
- Caspase-3 activation is crucial for GSDME cleavage and pyroptosis initiation.
Purpose of the Study:
- To investigate the roles of GSDME, caspase-3, and HMGB1 in lung cancer.
- To determine the clinical significance of these proteins in lung cancer tissues.
- To analyze their association with patient prognosis and CD8+ T cell infiltration.
Main Methods:
- Immunohistochemical staining was used to assess GSDME, caspase-3, and HMGB1 protein expression.
- Expression levels were correlated with clinical stage, pathological grade, and survival.
- CD8+ T cell accumulation was quantified and analyzed in relation to protein expression.
Main Results:
- Significant differences in GSDME, caspase-3, and HMGB1 expression were observed between lung cancer and paracancerous tissues.
- GSDME expression levels and lymph node invasion status were identified as prognostic indicators for lung cancer survival.
- HMGB1 showed a correlation with lymph node metastasis but was not a reliable prognostic indicator.
Conclusions:
- GSDME expression may serve as a significant prognostic biomarker for lung cancer survival.
- The prognostic impact of HMGB1 expression and CD8+ T cell abundance in lung cancer warrants further investigation.
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