Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration

Endometriosis (EMS) is a chronic disease that can cause dysmenorrhea, chronic pelvic pain, and infertility, among other symptoms. EMS diagnosis is often delayed compared to other chronic diseases, and there are currently no accurate, easily accessible, and non-invasive diagnostic tools. Therefore, i...

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Main Authors: Yi Huang, Qiong Li, Rui Hu, Ruiyun Li, Yuan Yang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.1011742/full
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author Yi Huang
Qiong Li
Rui Hu
Ruiyun Li
Yuan Yang
Yuan Yang
author_facet Yi Huang
Qiong Li
Rui Hu
Ruiyun Li
Yuan Yang
Yuan Yang
author_sort Yi Huang
collection DOAJ
description Endometriosis (EMS) is a chronic disease that can cause dysmenorrhea, chronic pelvic pain, and infertility, among other symptoms. EMS diagnosis is often delayed compared to other chronic diseases, and there are currently no accurate, easily accessible, and non-invasive diagnostic tools. Therefore, it is important to elucidate the mechanism of EMS and explore potential biomarkers and diagnostic tools for its accurate diagnosis and treatment. In the present study, we comprehensively analyzed the differential expression, immune infiltration, and interactions of EMS-related genes in three Homo sapiens datasets. Our results identified 332 differentially expressed genes (DEGs) associated with EMS. Gene ontology analysis showed that these changes mainly focused on the positive regulation of endometrial cell proliferation, cell metabolism, and extracellular space, and EMS involved the integrin, complement activation, folic acid metabolism, interleukin, and lipid signaling pathways. The LASSO regression model was established using immune DEGs with an area under the curve of 0.783 for the internal dataset and 0.656 for the external dataset. Five genes with diagnostic value, ACKR1, LMNB1, MFAP4, NMU, and SEMA3C, were screened from M1 and M2 macrophages, activated mast cells, neutrophils, natural killer cells, follicular T helper cells, CD8+, and CD4+ cells. A protein−protein interaction network based on the immune DEGs was constructed, and ten hub genes with the highest scores were identified. Our results may provide a framework for the development of pathological molecular networks in EMS.
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spelling doaj.art-eae905af06604e899b6e2bd07e75ec5a2022-12-22T04:07:40ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922022-10-011310.3389/fendo.2022.10117421011742Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltrationYi Huang0Qiong Li1Rui Hu2Ruiyun Li3Yuan Yang4Yuan Yang5The First Clinical Medical College, Lanzhou University, Lanzhou, ChinaDepartment of Obstetrics and Gynecology, Minqin People’s Hospital, Minqin, ChinaThe First Clinical Medical College, Lanzhou University, Lanzhou, ChinaThe First Clinical Medical College, Lanzhou University, Lanzhou, ChinaThe First Clinical Medical College, Lanzhou University, Lanzhou, ChinaThe Reproductive Medicine Center, The 1st Hospital of Lanzhou University, Lanzhou, ChinaEndometriosis (EMS) is a chronic disease that can cause dysmenorrhea, chronic pelvic pain, and infertility, among other symptoms. EMS diagnosis is often delayed compared to other chronic diseases, and there are currently no accurate, easily accessible, and non-invasive diagnostic tools. Therefore, it is important to elucidate the mechanism of EMS and explore potential biomarkers and diagnostic tools for its accurate diagnosis and treatment. In the present study, we comprehensively analyzed the differential expression, immune infiltration, and interactions of EMS-related genes in three Homo sapiens datasets. Our results identified 332 differentially expressed genes (DEGs) associated with EMS. Gene ontology analysis showed that these changes mainly focused on the positive regulation of endometrial cell proliferation, cell metabolism, and extracellular space, and EMS involved the integrin, complement activation, folic acid metabolism, interleukin, and lipid signaling pathways. The LASSO regression model was established using immune DEGs with an area under the curve of 0.783 for the internal dataset and 0.656 for the external dataset. Five genes with diagnostic value, ACKR1, LMNB1, MFAP4, NMU, and SEMA3C, were screened from M1 and M2 macrophages, activated mast cells, neutrophils, natural killer cells, follicular T helper cells, CD8+, and CD4+ cells. A protein−protein interaction network based on the immune DEGs was constructed, and ten hub genes with the highest scores were identified. Our results may provide a framework for the development of pathological molecular networks in EMS.https://www.frontiersin.org/articles/10.3389/fendo.2022.1011742/fullendometriosisdiagnosisimmune infiltrationCD8+pathological molecular networks
spellingShingle Yi Huang
Qiong Li
Rui Hu
Ruiyun Li
Yuan Yang
Yuan Yang
Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
Frontiers in Endocrinology
endometriosis
diagnosis
immune infiltration
CD8+
pathological molecular networks
title Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
title_full Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
title_fullStr Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
title_full_unstemmed Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
title_short Five immune-related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
title_sort five immune related genes as diagnostic markers for endometriosis and their correlation with immune infiltration
topic endometriosis
diagnosis
immune infiltration
CD8+
pathological molecular networks
url https://www.frontiersin.org/articles/10.3389/fendo.2022.1011742/full
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