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A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma
Pyroptosis has been proved to significantly influence the development of lung squamous cell carcinoma (LUSC). To better predict overall survival (OS) and provide guidance on the selection of therapy for LUSC patients, we constructed a novel prognostic biomarker based on pyroptosis-related genes. The...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685532/ https://www.ncbi.nlm.nih.gov/pubmed/36437960 http://dx.doi.org/10.3389/fgene.2022.996444 |
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author | Chen, Wei Wen, Min-Yu Yang, Kai-Bin Zheng, Li-Tao Li, Xuan |
author_facet | Chen, Wei Wen, Min-Yu Yang, Kai-Bin Zheng, Li-Tao Li, Xuan |
author_sort | Chen, Wei |
collection | PubMed |
description | Pyroptosis has been proved to significantly influence the development of lung squamous cell carcinoma (LUSC). To better predict overall survival (OS) and provide guidance on the selection of therapy for LUSC patients, we constructed a novel prognostic biomarker based on pyroptosis-related genes. The dataset for model construction were obtained from The Cancer Genome Atlas and the validation dataset were obtained from Gene Expression Omnibus. Differential expression genes between different pyroptosis expression patterns were identified. These genes were then used to construct pyroptosis expression pattern score (PEPScore) through weighted gene co-expression network analysis, univariate and multivariate cox regression analysis. Afterward, the differences in molecule and immune characteristics and the effect of different therapies were explored between the subgroups divided by the model. The PEPScore was constructed based on six pyroptosis-related genes (CSF2, FGA, AKAP12, CYP2C18, IRS4, TSLP). Compared with the high-PEPScore subgroup, the low-PEPScore subgroup had significantly better OS, higher TP53 and TTN mutation rate, higher infiltration of T follicular helper cells and CD8 T cells, and may benefit more from chemotherapeutic drugs, immunotherapy and radiotherapy. PEPScore is a prospective prognostic model to differentiate prognosis, molecular and immune microenvironmental features, as well as provide significant guidance for selecting clinical therapies. |
format | Online Article Text |
id | pubmed-9685532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96855322022-11-25 A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma Chen, Wei Wen, Min-Yu Yang, Kai-Bin Zheng, Li-Tao Li, Xuan Front Genet Genetics Pyroptosis has been proved to significantly influence the development of lung squamous cell carcinoma (LUSC). To better predict overall survival (OS) and provide guidance on the selection of therapy for LUSC patients, we constructed a novel prognostic biomarker based on pyroptosis-related genes. The dataset for model construction were obtained from The Cancer Genome Atlas and the validation dataset were obtained from Gene Expression Omnibus. Differential expression genes between different pyroptosis expression patterns were identified. These genes were then used to construct pyroptosis expression pattern score (PEPScore) through weighted gene co-expression network analysis, univariate and multivariate cox regression analysis. Afterward, the differences in molecule and immune characteristics and the effect of different therapies were explored between the subgroups divided by the model. The PEPScore was constructed based on six pyroptosis-related genes (CSF2, FGA, AKAP12, CYP2C18, IRS4, TSLP). Compared with the high-PEPScore subgroup, the low-PEPScore subgroup had significantly better OS, higher TP53 and TTN mutation rate, higher infiltration of T follicular helper cells and CD8 T cells, and may benefit more from chemotherapeutic drugs, immunotherapy and radiotherapy. PEPScore is a prospective prognostic model to differentiate prognosis, molecular and immune microenvironmental features, as well as provide significant guidance for selecting clinical therapies. Frontiers Media S.A. 2022-11-10 /pmc/articles/PMC9685532/ /pubmed/36437960 http://dx.doi.org/10.3389/fgene.2022.996444 Text en Copyright © 2022 Chen, Wen, Yang, Zheng and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Chen, Wei Wen, Min-Yu Yang, Kai-Bin Zheng, Li-Tao Li, Xuan A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
title | A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
title_full | A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
title_fullStr | A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
title_full_unstemmed | A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
title_short | A pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
title_sort | pyroptosis expression pattern score predicts prognosis and immune microenvironment of lung squamous cell carcinoma |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685532/ https://www.ncbi.nlm.nih.gov/pubmed/36437960 http://dx.doi.org/10.3389/fgene.2022.996444 |
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