Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients

This article contains further data and information from our published manuscript [1]. We aim to identify significant transcriptome alterations of vascular smooth muscle cells (VSMCs) in the aortic wall of myocardial infarction (MI) patients. Microarray gene analysis was applied to evaluate VSMCs of...

Full description

Bibliographic Details
Main Authors: Thidathip Wongsurawat, Chin Cheng Woo, Antonis Giannakakis, Xiao Yun Lin, Esther Sok Hwee Cheow, Chuen Neng Lee, Mark Richards, Siu Kwan Sze, Intawat Nookaew, Vladimir A. Kuznetsov, Vitaly Sorokin
Format: Article
Language:English
Published: Elsevier 2018-04-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340918301124
_version_ 1828177927281311744
author Thidathip Wongsurawat
Chin Cheng Woo
Antonis Giannakakis
Xiao Yun Lin
Esther Sok Hwee Cheow
Chuen Neng Lee
Mark Richards
Siu Kwan Sze
Intawat Nookaew
Vladimir A. Kuznetsov
Vitaly Sorokin
author_facet Thidathip Wongsurawat
Chin Cheng Woo
Antonis Giannakakis
Xiao Yun Lin
Esther Sok Hwee Cheow
Chuen Neng Lee
Mark Richards
Siu Kwan Sze
Intawat Nookaew
Vladimir A. Kuznetsov
Vitaly Sorokin
author_sort Thidathip Wongsurawat
collection DOAJ
description This article contains further data and information from our published manuscript [1]. We aim to identify significant transcriptome alterations of vascular smooth muscle cells (VSMCs) in the aortic wall of myocardial infarction (MI) patients. Microarray gene analysis was applied to evaluate VSMCs of MI and non-MI patients. Prediction Analysis of Microarray (PAM) identified genes that significantly discriminated the two groups of samples. Incorporation of gene ontology (GO) identified a VSMCs-associated classifier that discriminated between the two groups of samples. Mass spectrometry-based iTRAQ analysis revealed proteins significantly differentiating these two groups of samples. Ingenuity Pathway Analysis (IPA) revealed top pathways associated with hypoxia signaling in cardiovascular system. Enrichment analysis of these proteins suggested an activated pathway, and an integrated transcriptome-proteome pathway analysis revealed that it is the most implicated pathway. The intersection of the top candidate molecules from the transcriptome and proteome highlighted overexpression.
first_indexed 2024-04-12T05:06:29Z
format Article
id doaj.art-bf587bf85f4045279b34d359a1ffc5f3
institution Directory Open Access Journal
issn 2352-3409
language English
last_indexed 2024-04-12T05:06:29Z
publishDate 2018-04-01
publisher Elsevier
record_format Article
series Data in Brief
spelling doaj.art-bf587bf85f4045279b34d359a1ffc5f32022-12-22T03:46:52ZengElsevierData in Brief2352-34092018-04-011711121135Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patientsThidathip Wongsurawat0Chin Cheng Woo1Antonis Giannakakis2Xiao Yun Lin3Esther Sok Hwee Cheow4Chuen Neng Lee5Mark Richards6Siu Kwan Sze7Intawat Nookaew8Vladimir A. Kuznetsov9Vitaly Sorokin10Department of Genome and Gene Expression Data Analysis, Bioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, Singapore; Department of Biomedical Informatics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USADepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, SingaporeDepartment of Genome and Gene Expression Data Analysis, Bioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, SingaporeDepartment of Cardiac, Thoracic and Vascular Surgery, National University Heart Centre, Singapore, National University Health System, Singapore 119228, SingaporeSchool of Biological Sciences, Nanyang Technological University, Singapore 639798, SingaporeDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore; Department of Cardiac, Thoracic and Vascular Surgery, National University Heart Centre, Singapore, National University Health System, Singapore 119228, SingaporeCardiovascular Research Institute, National University Heart Centre, Singapore, 119228, Singapore; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, SingaporeSchool of Biological Sciences, Nanyang Technological University, Singapore 639798, SingaporeDepartment of Biomedical Informatics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USADepartment of Genome and Gene Expression Data Analysis, Bioinformatics Institute, Agency for Science, Technology and Research (A*STAR), Singapore 138671, Singapore; School of Computer Science and Engineering, Nanyang Technological University, Singapore 639798, SingaporeDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore; Department of Cardiac, Thoracic and Vascular Surgery, National University Heart Centre, Singapore, National University Health System, Singapore 119228, Singapore; Corresponding author at: Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.This article contains further data and information from our published manuscript [1]. We aim to identify significant transcriptome alterations of vascular smooth muscle cells (VSMCs) in the aortic wall of myocardial infarction (MI) patients. Microarray gene analysis was applied to evaluate VSMCs of MI and non-MI patients. Prediction Analysis of Microarray (PAM) identified genes that significantly discriminated the two groups of samples. Incorporation of gene ontology (GO) identified a VSMCs-associated classifier that discriminated between the two groups of samples. Mass spectrometry-based iTRAQ analysis revealed proteins significantly differentiating these two groups of samples. Ingenuity Pathway Analysis (IPA) revealed top pathways associated with hypoxia signaling in cardiovascular system. Enrichment analysis of these proteins suggested an activated pathway, and an integrated transcriptome-proteome pathway analysis revealed that it is the most implicated pathway. The intersection of the top candidate molecules from the transcriptome and proteome highlighted overexpression.http://www.sciencedirect.com/science/article/pii/S2352340918301124
spellingShingle Thidathip Wongsurawat
Chin Cheng Woo
Antonis Giannakakis
Xiao Yun Lin
Esther Sok Hwee Cheow
Chuen Neng Lee
Mark Richards
Siu Kwan Sze
Intawat Nookaew
Vladimir A. Kuznetsov
Vitaly Sorokin
Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
Data in Brief
title Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
title_full Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
title_fullStr Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
title_full_unstemmed Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
title_short Transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
title_sort transcriptome alterations of vascular smooth muscle cells in aortic wall of myocardial infarction patients
url http://www.sciencedirect.com/science/article/pii/S2352340918301124
work_keys_str_mv AT thidathipwongsurawat transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT chinchengwoo transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT antonisgiannakakis transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT xiaoyunlin transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT esthersokhweecheow transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT chuennenglee transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT markrichards transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT siukwansze transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT intawatnookaew transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT vladimirakuznetsov transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients
AT vitalysorokin transcriptomealterationsofvascularsmoothmusclecellsinaorticwallofmyocardialinfarctionpatients