Multiomics Analysis of Disulfidptosis Patterns and Integrated Machine Learning to Predict Immunotherapy Response in Lung Adenocarcinoma
- Authors: Liu J.1, Li H.2, Zhang N.3, Dong Q.4, Liang Z.5
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Affiliations:
- Department of Otorhinolaryngology, Tianjin Medical University General Hospita
- Laboratory of Cancer Cell Biology, National Clinical Research Center for Cancer
- Department of Otorhinolaryngology, Tianjin Medical University General Hospital
- Laboratory of Cancer Cell Biology, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer
- Department of Otorhinolaryngology, TianjiTianjin Medical University General Hospital
- Issue: Vol 31, No 25 (2024)
- Pages: 4034-4055
- Section: Anti-Infectives and Infectious Diseases
- URL: https://cijournal.ru/0929-8673/article/view/644919
- DOI: https://doi.org/10.2174/0109298673313281240425050032
- ID: 644919
Cite item
Full Text
Abstract
Background:Recent studies have unveiled disulfidptosis as a phenomenon intimately associated with cellular damage, heralding new avenues for exploring tumor cell dynamics. We aimed to explore the impact of disulfide cell death on the tumor immune microenvironment and immunotherapy in lung adenocarcinoma (LUAD).
Methods:We initially utilized pan-cancer transcriptomics to explore the expression, prognosis, and mutation status of genes related to disulfidptosis. Using the LUAD multi- -omics cohorts in the TCGA database, we explore the molecular characteristics of subtypes related to disulfidptosis. Employing various machine learning algorithms, we construct a robust prognostic model to predict immune therapy responses and explore the model's impact on the tumor microenvironment through single-cell transcriptome data. Finally, the biological functions of genes related to the prognostic model are verified through laboratory experiments.
Results:Genes related to disulfidptosis exhibit high expression and significant prognostic value in various cancers, including LUAD. Two disulfidptosis subtypes with distinct prognoses and molecular characteristics have been identified, leading to the development of a robust DSRS prognostic model, where a lower risk score correlates with a higher response rate to immunotherapy and a better patient prognosis. NAPSA, a critical gene in the risk model, was found to inhibit the proliferation and migration of LUAD cells.
Conclusion:Our research introduces an innovative prognostic risk model predicated upon disulfidptosis genes for patients afflicted with Lung Adenocarcinoma (LUAD). This model proficiently forecasts the survival rates and therapeutic outcomes for LUAD patients, thereby delineating the high-risk population with distinctive immune cell infiltration and a state of immunosuppression. Furthermore, NAPSA can inhibit the proliferation and invasion capabilities of LUAD cells, thereby identifying new molecules for clinical targeted therapy.
About the authors
Junzhi Liu
Department of Otorhinolaryngology, Tianjin Medical University General Hospita
Email: info@benthamscience.net
Huimin Li
Laboratory of Cancer Cell Biology, National Clinical Research Center for Cancer
Email: info@benthamscience.net
Nannan Zhang
Department of Otorhinolaryngology, Tianjin Medical University General Hospital
Email: info@benthamscience.net
Qiuping Dong
Laboratory of Cancer Cell Biology, Tianjin Medical University Cancer Institute & Hospital, National Clinical Research Center for Cancer
Email: info@benthamscience.net
Zheng Liang
Department of Otorhinolaryngology, TianjiTianjin Medical University General Hospital
Author for correspondence.
Email: info@benthamscience.net
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Supplementary files
