Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans

Background: Thromboangiitis obliterans (TAO) causes vascular insufficiency due to chronic inflammation and abrupt thrombosis of the medium and small arteries of the extremities. In our study, we aimed to determine biomarkers for the diagnosis of TAO by evaluating 15 male TAO patients with Shinoya di...

Full description

Bibliographic Details
Main Authors: Gözde Öztan, Nilgün Bozbuğa, Halim İşsever, Fatma Oğuz, İrem Canıaz, Nilgün Yazıksız, Melike Ertan, İbrahim Ufuk Alpagut
Format: Article
Language:English
Published: MDPI AG 2023-12-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/15/1/19
_version_ 1797343872973537280
author Gözde Öztan
Nilgün Bozbuğa
Halim İşsever
Fatma Oğuz
İrem Canıaz
Nilgün Yazıksız
Melike Ertan
İbrahim Ufuk Alpagut
author_facet Gözde Öztan
Nilgün Bozbuğa
Halim İşsever
Fatma Oğuz
İrem Canıaz
Nilgün Yazıksız
Melike Ertan
İbrahim Ufuk Alpagut
author_sort Gözde Öztan
collection DOAJ
description Background: Thromboangiitis obliterans (TAO) causes vascular insufficiency due to chronic inflammation and abrupt thrombosis of the medium and small arteries of the extremities. In our study, we aimed to determine biomarkers for the diagnosis of TAO by evaluating 15 male TAO patients with Shinoya diagnostic criteria and 5 healthy controls who did not have TAO-related symptoms in their family histories. Methods: The Clariom D Affymetrix platform was used to conduct microarray analysis on total RNA extracted from whole blood. A total of 477 genes (FC ≤ 5 or >5) common to the fifteen patient and five control samples were selected using comparative microarray analysis; among them, 79 genes were upregulated and 398 genes were downregulated. Results: According to FC ≤ 10 or >10, in the same TAO patient and control group, 13 genes out of 28 were upregulated, whereas 15 genes were downregulated. The 11 key genes identified according to their mean log2FC values were <i>PLP2, RPL27A, CCL4, FMNL1, EGR1, EIF4A1, RPL9, LAMP2, RNF149, EIF4G2,</i> and <i>DGKZ</i>. The genes were ranked according to their relative expression as follows: <i>FMNL1</i> > <i>RNF149</i> > <i>RPL27A</i> > <i>EIF4G2</i> > <i>EIF4A1</i> > <i>LAMP2</i> > <i>EGR1</i> > <i>PLP2</i> > <i>DGKZ</i> > <i>RPL9</i> > <i>CCL4.</i> Using protein–protein interaction network analysis, <i>RPL9, RPL27A,</i> and <i>RPL32</i> were found to be closely related to EIF4G2 and EIF4A1. The Reactome pathway found pathways linked to 28 genes. These pathways included the immune system, cellular responses to stress, cytokine signaling in the immune system, and signaling by ROBO receptors. Conclusions: By figuring out the protein expression levels of the genes that have been found to explain how TAO disease works at the molecular level, it will be possible to figure out how well these chosen transcripts can diagnose and predict the disease.
first_indexed 2024-03-08T10:54:08Z
format Article
id doaj.art-43f2e05c22af4f4e87036a740601d833
institution Directory Open Access Journal
issn 2073-4425
language English
last_indexed 2024-03-08T10:54:08Z
publishDate 2023-12-01
publisher MDPI AG
record_format Article
series Genes
spelling doaj.art-43f2e05c22af4f4e87036a740601d8332024-01-26T16:41:23ZengMDPI AGGenes2073-44252023-12-011511910.3390/genes15010019Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis ObliteransGözde Öztan0Nilgün Bozbuğa1Halim İşsever2Fatma Oğuz3İrem Canıaz4Nilgün Yazıksız5Melike Ertan6İbrahim Ufuk Alpagut7Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Cardiovascular Surgery, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Public Health, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Cardiovascular Surgery, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Cardiovascular Surgery, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Cardiovascular Surgery, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyDepartment of Cardiovascular Surgery, Istanbul Faculty of Medicine, Istanbul University, Topkapi, 34093 Istanbul, TurkeyBackground: Thromboangiitis obliterans (TAO) causes vascular insufficiency due to chronic inflammation and abrupt thrombosis of the medium and small arteries of the extremities. In our study, we aimed to determine biomarkers for the diagnosis of TAO by evaluating 15 male TAO patients with Shinoya diagnostic criteria and 5 healthy controls who did not have TAO-related symptoms in their family histories. Methods: The Clariom D Affymetrix platform was used to conduct microarray analysis on total RNA extracted from whole blood. A total of 477 genes (FC ≤ 5 or >5) common to the fifteen patient and five control samples were selected using comparative microarray analysis; among them, 79 genes were upregulated and 398 genes were downregulated. Results: According to FC ≤ 10 or >10, in the same TAO patient and control group, 13 genes out of 28 were upregulated, whereas 15 genes were downregulated. The 11 key genes identified according to their mean log2FC values were <i>PLP2, RPL27A, CCL4, FMNL1, EGR1, EIF4A1, RPL9, LAMP2, RNF149, EIF4G2,</i> and <i>DGKZ</i>. The genes were ranked according to their relative expression as follows: <i>FMNL1</i> > <i>RNF149</i> > <i>RPL27A</i> > <i>EIF4G2</i> > <i>EIF4A1</i> > <i>LAMP2</i> > <i>EGR1</i> > <i>PLP2</i> > <i>DGKZ</i> > <i>RPL9</i> > <i>CCL4.</i> Using protein–protein interaction network analysis, <i>RPL9, RPL27A,</i> and <i>RPL32</i> were found to be closely related to EIF4G2 and EIF4A1. The Reactome pathway found pathways linked to 28 genes. These pathways included the immune system, cellular responses to stress, cytokine signaling in the immune system, and signaling by ROBO receptors. Conclusions: By figuring out the protein expression levels of the genes that have been found to explain how TAO disease works at the molecular level, it will be possible to figure out how well these chosen transcripts can diagnose and predict the disease.https://www.mdpi.com/2073-4425/15/1/19TAOBuerger’s diseasemicroarray analysisgenesClariom D arraydiagnostic markers
spellingShingle Gözde Öztan
Nilgün Bozbuğa
Halim İşsever
Fatma Oğuz
İrem Canıaz
Nilgün Yazıksız
Melike Ertan
İbrahim Ufuk Alpagut
Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans
Genes
TAO
Buerger’s disease
microarray analysis
genes
Clariom D array
diagnostic markers
title Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans
title_full Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans
title_fullStr Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans
title_full_unstemmed Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans
title_short Comparative Analysis of Transcriptome Profiles in Patients with Thromboangiitis Obliterans
title_sort comparative analysis of transcriptome profiles in patients with thromboangiitis obliterans
topic TAO
Buerger’s disease
microarray analysis
genes
Clariom D array
diagnostic markers
url https://www.mdpi.com/2073-4425/15/1/19
work_keys_str_mv AT gozdeoztan comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT nilgunbozbuga comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT halimissever comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT fatmaoguz comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT iremcanıaz comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT nilgunyazıksız comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT melikeertan comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans
AT ibrahimufukalpagut comparativeanalysisoftranscriptomeprofilesinpatientswiththromboangiitisobliterans