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Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity
BACKGROUND: Endometrial cancer (EC) is one of the worldwide gynecological malignancies. Endoplasmic reticulum (ER) stress is the cellular homeostasis disturbance that participates in cancer progression. However, the mechanisms of ER Stress on EC have not been fully elucidated. METHOD: The ER Stress-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599039/ https://www.ncbi.nlm.nih.gov/pubmed/37880674 http://dx.doi.org/10.1186/s12920-023-01679-5 |
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author | Zhang, Tang ansu Zhang, Qian Zhang, Jun Zhao, Rong Shi, Rui Wei, Sitian Liu, Shuangge Zhang, Qi Wang, Hongbo |
author_facet | Zhang, Tang ansu Zhang, Qian Zhang, Jun Zhao, Rong Shi, Rui Wei, Sitian Liu, Shuangge Zhang, Qi Wang, Hongbo |
author_sort | Zhang, Tang ansu |
collection | PubMed |
description | BACKGROUND: Endometrial cancer (EC) is one of the worldwide gynecological malignancies. Endoplasmic reticulum (ER) stress is the cellular homeostasis disturbance that participates in cancer progression. However, the mechanisms of ER Stress on EC have not been fully elucidated. METHOD: The ER Stress-related genes were obtained from Gene Set Enrichment Analysis (GSEA) and GeneCards, and the RNA-seq and clinical data were downloaded from The Cancer Genome Atlas (TCGA). The risk signature was constructed by the Cox regression and the least absolute shrinkage and selection operator (LASSO) analysis. The significance of the risk signature and clinical factors were tested by time-dependent receiver operating characteristic (ROC) curves, and the selected were to build a nomogram. The immunity correlation was particularly analyzed, including the related immune cells, pathways, and immune checkpoints. Functional enrichment, potential chemotherapies, and in vitro validation were also conducted. RESULT: An ER Stress-based risk signature, consisting of TRIB3, CREB3L3, XBP1, and PPP1R15A was established. Patients were randomly divided into training and testing groups with 1:1 ratio for subsequent calculation and validation. Based on risk scores, high- and low-risk subgroups were classified, and low-risk subgroup demonstrated better prognosis. The Area Under Curve (AUC) demonstrated a reliable predictive capability of the risk signature. The majority of significantly different immune cells and pathways were enriched more in low-risk subgroup. Similarly, several typical immune checkpoints, expressed higher in low-risk subgroup. Patients of the two subgroups responded differently to chemotherapies. CONCLUSION: We established an ER Stress-based risk signature that could effectively predict EC patients’ prognosis and their immune correlation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01679-5. |
format | Online Article Text |
id | pubmed-10599039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105990392023-10-26 Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity Zhang, Tang ansu Zhang, Qian Zhang, Jun Zhao, Rong Shi, Rui Wei, Sitian Liu, Shuangge Zhang, Qi Wang, Hongbo BMC Med Genomics Research BACKGROUND: Endometrial cancer (EC) is one of the worldwide gynecological malignancies. Endoplasmic reticulum (ER) stress is the cellular homeostasis disturbance that participates in cancer progression. However, the mechanisms of ER Stress on EC have not been fully elucidated. METHOD: The ER Stress-related genes were obtained from Gene Set Enrichment Analysis (GSEA) and GeneCards, and the RNA-seq and clinical data were downloaded from The Cancer Genome Atlas (TCGA). The risk signature was constructed by the Cox regression and the least absolute shrinkage and selection operator (LASSO) analysis. The significance of the risk signature and clinical factors were tested by time-dependent receiver operating characteristic (ROC) curves, and the selected were to build a nomogram. The immunity correlation was particularly analyzed, including the related immune cells, pathways, and immune checkpoints. Functional enrichment, potential chemotherapies, and in vitro validation were also conducted. RESULT: An ER Stress-based risk signature, consisting of TRIB3, CREB3L3, XBP1, and PPP1R15A was established. Patients were randomly divided into training and testing groups with 1:1 ratio for subsequent calculation and validation. Based on risk scores, high- and low-risk subgroups were classified, and low-risk subgroup demonstrated better prognosis. The Area Under Curve (AUC) demonstrated a reliable predictive capability of the risk signature. The majority of significantly different immune cells and pathways were enriched more in low-risk subgroup. Similarly, several typical immune checkpoints, expressed higher in low-risk subgroup. Patients of the two subgroups responded differently to chemotherapies. CONCLUSION: We established an ER Stress-based risk signature that could effectively predict EC patients’ prognosis and their immune correlation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01679-5. BioMed Central 2023-10-25 /pmc/articles/PMC10599039/ /pubmed/37880674 http://dx.doi.org/10.1186/s12920-023-01679-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhang, Tang ansu Zhang, Qian Zhang, Jun Zhao, Rong Shi, Rui Wei, Sitian Liu, Shuangge Zhang, Qi Wang, Hongbo Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
title | Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
title_full | Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
title_fullStr | Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
title_full_unstemmed | Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
title_short | Identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
title_sort | identification of the role of endoplasmic reticulum stress genes in endometrial cancer and their association with tumor immunity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599039/ https://www.ncbi.nlm.nih.gov/pubmed/37880674 http://dx.doi.org/10.1186/s12920-023-01679-5 |
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