Evaluation of molecular apoptosis signaling pathways and its correlation with EBV viral load in SLE patients using systems biology approach.


Journal

Human antibodies
ISSN: 1875-869X
Titre abrégé: Hum Antibodies
Pays: Netherlands
ID NLM: 9711270

Informations de publication

Date de publication:
2022
Historique:
pubmed: 6 12 2021
medline: 3 3 2022
entrez: 5 12 2021
Statut: ppublish

Résumé

Considerable evidence supports that SLE could be related to apoptotic cells and EBV infection. The aim of this study was to identify the transcriptional signature of EBV infection in SLE patients for survey of the molecular apoptosis signaling pathways. The PBMCs gene expression profiles of healthy control and SLE patients were obtained from GEO. Functional annotation and signaling pathway enrichment were carried out using DAVID, KEGG. To validate bioinformatics analysis the changes in genes expression of some of obtained genes, Real time PCR was performed on PBMCs from 28 SLE patients and 18 controls. We found that mean viral load was 6013 ± 390.1 copy/μg DNA from PBMCs in all patients. QRT-PCR results showed that the expression of the DUSP1 and LAMP3 genes which had most changes in the logFC among 4 candidate genes, increased significantly in comparison with control. The consistent expression of LMP2 as viral latency gene involve in apoptosis signaling pathways was detected in SLE patients with EBV viral load and some controls. The study indicated that some cellular genes may have an important role in pathogenesis of SLE through apoptosis signaling pathways. Beside, EBV infection as an environmental risk factor for SLE may affect the dysfunction of apoptosis.

Sections du résumé

BACKGROUND BACKGROUND
Considerable evidence supports that SLE could be related to apoptotic cells and EBV infection.
OBJECTIVE OBJECTIVE
The aim of this study was to identify the transcriptional signature of EBV infection in SLE patients for survey of the molecular apoptosis signaling pathways.
METHODS METHODS
The PBMCs gene expression profiles of healthy control and SLE patients were obtained from GEO. Functional annotation and signaling pathway enrichment were carried out using DAVID, KEGG. To validate bioinformatics analysis the changes in genes expression of some of obtained genes, Real time PCR was performed on PBMCs from 28 SLE patients and 18 controls.
RESULTS RESULTS
We found that mean viral load was 6013 ± 390.1 copy/μg DNA from PBMCs in all patients. QRT-PCR results showed that the expression of the DUSP1 and LAMP3 genes which had most changes in the logFC among 4 candidate genes, increased significantly in comparison with control. The consistent expression of LMP2 as viral latency gene involve in apoptosis signaling pathways was detected in SLE patients with EBV viral load and some controls.
CONCLUSIONS CONCLUSIONS
The study indicated that some cellular genes may have an important role in pathogenesis of SLE through apoptosis signaling pathways. Beside, EBV infection as an environmental risk factor for SLE may affect the dysfunction of apoptosis.

Identifiants

pubmed: 34864653
pii: HAB211505
doi: 10.3233/HAB-211505
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

37-46

Auteurs

Soad Ghabeshi (S)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Ali Najafi (A)

Molecular Biology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Batol Zamani (B)

Autoimmune Diseases Research Center, Kashan University of Medical Sciences, Kashan, Iran.

Mozhdeh Soltani (M)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Amanuel Godana Arero (AG)

Students' Scientific Research Center (SSRC), Tehran University of Medical Sciences, Tehran, Iran.
Universal Scientific Education and Research Network (USERN), Tehran, Iran.

Shim Izadi (S)

Virology Department, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

Ahmad Piroozmand (A)

Autoimmune Diseases Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Department of Microbiology, School of Medicine, Kashan University of Medical Sciences, Kashan, Iran.

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Classifications MeSH