Comprehensive analysis of a pyroptosis-related gene signature of clinical and biological value in acute myeloid leukaemia
•Construction of a PRGs Prognostic Model in AML Patients.•The PRGs Prognostic Model has good predictive value in AML patients.•Pyroptosis serves an essential function in anti-leukemia treatment. Acutemyeloidleukaemia(AML) is an illness of varied origin and unpredictable prognosis. Pyroptosis, a nove...
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Veröffentlicht in: | International immunopharmacology 2022-07, Vol.108, p.108802-108802, Article 108802 |
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Sprache: | eng |
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Zusammenfassung: | •Construction of a PRGs Prognostic Model in AML Patients.•The PRGs Prognostic Model has good predictive value in AML patients.•Pyroptosis serves an essential function in anti-leukemia treatment.
Acutemyeloidleukaemia(AML) is an illness of varied origin and unpredictable prognosis. Pyroptosis, a novel class of gasdermin-mediated programmed cell death (PCD), serves a critical function in anti-leukemia. But, the correlation between pyroptosis-related genes (PRGs) and AML prognosis is undetermined. Here, we obtained the RNA profile and matched clinical information of AML patients from the TCGA and GEO databases. 6 PRGs were identified to be strongly related to AML prognosis via univariate COX analysis. Next, the LASSO regression analysis was used to develop a PRG signature for AML prognosis, which was then employed for the stratification of patients into a low- (LR) or high-risk (HR) group. Kaplan-Meier analysis revealed that the HR group, but not the LR group, had worse prognosis. In addition, ROC curve analysis revealed that our prognotic model had good predictive value. Functional enrichment analysis indicated that the immune status was remarkably different between the two risk groups. In vitro experiments demonstrated that pyroptosis serves an essential function in anti-leukemia treatment. In summary, our newly developed model has good predictive value and can offer guidance into the precise estimation of AML prognosis and targeting pyroptosis is a potential therapeutic alternative for AML. |
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ISSN: | 1567-5769 1878-1705 |
DOI: | 10.1016/j.intimp.2022.108802 |