# Pyroptosis-Related Gene Signatures Enable Robustly Diagnosis, Prognosis and Immune Responses Prediction in Uterine Corpus Endometrial Carcinoma

**Authors:** Xuanming Chen, Xiangyu Jin, Jiafu Wang, Hanfei Li, Chuanfang Wu, Jinku Bao

PMC · DOI: 10.7150/jca.104826 · Journal of Cancer · 2025-05-08

## TL;DR

This study identifies pyroptosis-related genes that can help diagnose, predict prognosis, and assess immune responses in uterine corpus endometrial carcinoma.

## Contribution

The study introduces novel pyroptosis-related gene signatures for UCEC diagnosis, prognosis, and immune response prediction.

## Key findings

- 26 pyroptosis-related genes were identified as associated with UCEC diagnosis and prognosis.
- A logistic regression classifier performed best in predicting UCEC outcomes.
- The PRGRS model independently predicted prognosis and correlated with tumor immune responses.

## Abstract

Purpose: Uterine corpus endometrial carcinoma (UCEC) is a gynecological malignancy with poor prognosis and high lethality rates. Pyroptosis, a pro-inflammatory programmed cell death pattern, significantly influences tumor growth, development, and metastasis. We intend to explore whether pyroptosis-related genes can be screened as targets for early detection and patient prognosis.

Methods: We used nine common machine learning algorithms to build classifiers based on the pyroptosis-related genes, evaluated the classifiers' performance using metrics like the receiver operating characteristic curve (ROC), and verified the results using external datasets. Using Least Absolute Shrinkage and Selection Operator (LASSO) regression analysis, we built a predictive model. ROC and univariate/multivariate Cox analyses were used to assess the model's performance and its independence in predicting patient prognosis. We used a variety of statistical methods and algorithms to investigate the connection between tumor immunity and pyroptosis-related genes.

Results: We identified 26 pyroptosis-related genes associated with the diagnosis and prognosis of UCEC. We found the logistic regression classifier performing the best. We then constructed a predictive model based on seven PRGs about IRF2, TIRAP, BAK1, GSDMD, CHMP2A, GPX4, CHMP2B. The pyroptosis-related gene risk signature (PRGRS) effectively classified UCEC patients. We demonstrated that PRGRS independently impacted UCEC prognosis and confirmed its expression using qRT-PCR experiments. Furthermore, we found associations between PRGRS and tumor immune response.

Conclusion: Our study highlights novel pyroptosis-related gene signatures that may be utilized for early screening and prognosis prediction in UCEC patients, offering potential targets for future research and guidance for personalized anticancer therapies.

## Linked entities

- **Genes:** IRF2 (interferon regulatory factor 2) [NCBI Gene 3660], TIRAP (TIR domain containing adaptor protein) [NCBI Gene 114609], BAK1 (BCL2 antagonist/killer 1) [NCBI Gene 578], GSDMD (gasdermin D) [NCBI Gene 79792], CHMP2A (charged multivesicular body protein 2A) [NCBI Gene 27243], GPX4 (glutathione peroxidase 4) [NCBI Gene 2879], CHMP2B (charged multivesicular body protein 2B) [NCBI Gene 25978]
- **Diseases:** Uterine Corpus Endometrial Carcinoma (MONDO:0000553)

## Full-text entities

- **Genes:** TIRAP (TIR domain containing adaptor protein) [NCBI Gene 114609] {aka BACTS1, Mal, MyD88-2, wyatt}, CHMP2A (charged multivesicular body protein 2A) [NCBI Gene 27243] {aka BC-2, BC2, CHMP2, VPS2, VPS2A}, BAK1 (BCL2 antagonist/killer 1) [NCBI Gene 578] {aka BAK, BAK-LIKE, BCL2L7, CDN1}, GSDMD (gasdermin D) [NCBI Gene 79792] {aka DF5L, DFNA5L, FKSG10, GSDMDC1}, IRF2 (interferon regulatory factor 2) [NCBI Gene 3660] {aka IRF-2}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, CHMP2B (charged multivesicular body protein 2B) [NCBI Gene 25978] {aka ALS17, CHMP2.5, DMT1, FTDALS7, VPS2-2, VPS2B}
- **Diseases:** gynecological malignancy (MESH:D005833), inflammatory (MESH:D007249), metastasis (MESH:D009362), tumor (MESH:D009369), UCEC (MESH:D016889)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

96 references — full list in the complete paper: https://tomesphere.com/paper/PMC12171010/full.md

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Source: https://tomesphere.com/paper/PMC12171010