Cargando…

Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis

BACKGROUND: Neural tube defects (NTDs) are one of the most common types of birth defects. Oral folic acid (FA) prophylaxis is currently available, but the pathogenesis of NTDs is not fully understood. We conducted this study to examine the role of the immune landscape of NTDs and identify novel diag...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Qingli, Yang, Li, Nong, Binbin, Gan, Haisi, Wu, Huizhen, Li, Meiyan, Jin, Mingyang, Xie, Liling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347061/
https://www.ncbi.nlm.nih.gov/pubmed/35928755
http://dx.doi.org/10.21037/atm-22-1273
_version_ 1784761782554853376
author Huang, Qingli
Yang, Li
Nong, Binbin
Gan, Haisi
Wu, Huizhen
Li, Meiyan
Jin, Mingyang
Xie, Liling
author_facet Huang, Qingli
Yang, Li
Nong, Binbin
Gan, Haisi
Wu, Huizhen
Li, Meiyan
Jin, Mingyang
Xie, Liling
author_sort Huang, Qingli
collection PubMed
description BACKGROUND: Neural tube defects (NTDs) are one of the most common types of birth defects. Oral folic acid (FA) prophylaxis is currently available, but the pathogenesis of NTDs is not fully understood. We conducted this study to examine the role of the immune landscape of NTDs and identify novel diagnostic and therapeutic biomarkers. METHODS: We downloaded the GSE33111 data set of 12 NTD embryos and 12 healthy embryos in the same period of fetal development from the Gene Expression Omnibus (GEO) database. We compared the healthy embryos and NTD embryos to identify the differentially expressed genes (DEGs). We also performed a functional enrichment analysis of the DEGs using the clusterProfiler package. We extracted the top 10 ranked genes as hub immune-related biomarkers. We then used receiver operating characteristic (ROC) curves to determine the expression levels of the hub immune-related genes and the accuracy of the diagnosis of NTDs. Finally, we analyzed the immune landscape of the NTD embryos and healthy embryos via a single-sample gene set enrichment analysis (ssGSEA). RESULTS: A total of 611 DEGs were identified by the differential analysis, including 95 immune genes. The functional enrichment analysis indicated that Epstein-Barr virus infection, antigen processing and presentation, inflammatory bowel disease, and type I diabetes mellitus were associated with NTDs. The results of the expression level analysis showed that the hub immune-related genes were more highly expressed in the NTD embryos than the healthy embryos. Additionally, the ROC curve analysis also indicated that the expression levels of the 10 hub immune-related genes were highly accurate in the diagnosis of NTDs [area under the curve (AUC) range, 0.708–0.812]. The immune infiltration analysis demonstrated that 20 of the 28 immune cell types were more highly infiltrated in the NTD embryos than the healthy embryos. CONCLUSIONS: Immune-related genes are important regulators of the occurrence and development of NTDs.
format Online
Article
Text
id pubmed-9347061
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-93470612022-08-03 Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis Huang, Qingli Yang, Li Nong, Binbin Gan, Haisi Wu, Huizhen Li, Meiyan Jin, Mingyang Xie, Liling Ann Transl Med Original Article BACKGROUND: Neural tube defects (NTDs) are one of the most common types of birth defects. Oral folic acid (FA) prophylaxis is currently available, but the pathogenesis of NTDs is not fully understood. We conducted this study to examine the role of the immune landscape of NTDs and identify novel diagnostic and therapeutic biomarkers. METHODS: We downloaded the GSE33111 data set of 12 NTD embryos and 12 healthy embryos in the same period of fetal development from the Gene Expression Omnibus (GEO) database. We compared the healthy embryos and NTD embryos to identify the differentially expressed genes (DEGs). We also performed a functional enrichment analysis of the DEGs using the clusterProfiler package. We extracted the top 10 ranked genes as hub immune-related biomarkers. We then used receiver operating characteristic (ROC) curves to determine the expression levels of the hub immune-related genes and the accuracy of the diagnosis of NTDs. Finally, we analyzed the immune landscape of the NTD embryos and healthy embryos via a single-sample gene set enrichment analysis (ssGSEA). RESULTS: A total of 611 DEGs were identified by the differential analysis, including 95 immune genes. The functional enrichment analysis indicated that Epstein-Barr virus infection, antigen processing and presentation, inflammatory bowel disease, and type I diabetes mellitus were associated with NTDs. The results of the expression level analysis showed that the hub immune-related genes were more highly expressed in the NTD embryos than the healthy embryos. Additionally, the ROC curve analysis also indicated that the expression levels of the 10 hub immune-related genes were highly accurate in the diagnosis of NTDs [area under the curve (AUC) range, 0.708–0.812]. The immune infiltration analysis demonstrated that 20 of the 28 immune cell types were more highly infiltrated in the NTD embryos than the healthy embryos. CONCLUSIONS: Immune-related genes are important regulators of the occurrence and development of NTDs. AME Publishing Company 2022-05 /pmc/articles/PMC9347061/ /pubmed/35928755 http://dx.doi.org/10.21037/atm-22-1273 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Huang, Qingli
Yang, Li
Nong, Binbin
Gan, Haisi
Wu, Huizhen
Li, Meiyan
Jin, Mingyang
Xie, Liling
Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
title Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
title_full Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
title_fullStr Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
title_full_unstemmed Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
title_short Identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
title_sort identification of immune-related biomarkers in embryos with neural tube defects via a bioinformatics analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9347061/
https://www.ncbi.nlm.nih.gov/pubmed/35928755
http://dx.doi.org/10.21037/atm-22-1273
work_keys_str_mv AT huangqingli identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT yangli identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT nongbinbin identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT ganhaisi identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT wuhuizhen identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT limeiyan identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT jinmingyang identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis
AT xieliling identificationofimmunerelatedbiomarkersinembryoswithneuraltubedefectsviaabioinformaticsanalysis