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pmid:27275413

Comprehensive and computational analysis of genes in human umbilical vein endothelial cells responsive to X-irradiation.

Yukihiro Furusawa · Qing-Li Zhao · Yuichi Hattori · Yoshiaki Tabuchi · Toshiyasu Iwasaki · Takaharu Nomura · Takashi Kondo

Genomics data · 2016 doi:10.1016/j.gdata.2016.05.007

Paper

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Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:27275413
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science-record
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paper object · 10 fields
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title
Comprehensive and computational analysis of genes in human umbilical vein endothelial cells responsive to X-irradiation.
doi
10.1016/j.gdata.2016.05.007
pmid
27275413
authors array · 7 items
[0]
Yukihiro Furusawa
[1]
Qing-Li Zhao
[2]
Yuichi Hattori
[3]
Yoshiaki Tabuchi
[4]
Toshiyasu Iwasaki
[5]
Takaharu Nomura
[6]
Takashi Kondo
journal
Genomics data
year
2016
abstract
Radiation exposure such as A-bomb or radiation therapy is considered a major health-risk factor for cardiovascular disease. In order to understand the molecular mechanisms underlying the inflammatory reaction frequently encountered in the vascular system after exposure to ionizing radiation, we carried out a global scale microarray and computational gene expression analyses on human umbilical endothelial cells (HUVECs) exposed to X-ray (2.5 Gy). The gene ontology analysis revealed that the down-regulated genes were associated with cell cycle regulation, whereas the up-regulated genes were associated with inflammatory responses, in particular, the type 1 interferon response. The computational analysis using ingenuity pathway analysis also identified a gene network containing the interferon response factor 7 (IRF7) and its transcriptional targets such as interferon-induced transcripts (IFITs) and Mx1, which have been known to be associated with inflammation in endothelial cells. The up-regulated genes and the gene network identified here may explain the inflammatory response induced by X-irradiation. These findings uncover part of the molecular basis of the mechanism(s) of the inflammatory disorder in response to X-irradiation in HUVECs. The dataset is publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession number GSE76484.
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Principal component analysis (PCA), gene ontology (GO) analysis, and hierarchical clustering from the obtained normalized intensity data were performed using GeneSpring® software (Agilent).
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sections[8] "Gene expression analysis" paragraph 3
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Principal component analysis (PCA), gene ontology (GO) analysis, and hierarchical clustering from the obtained normalized intensity data were performed using GeneSpring® software (Agilent).
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The dataset is publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession number GSE76484.
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The dataset is publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession number GSE76484.
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Global-scale microarray and computational gene-expression analysis showed that 2.5 Gy X-irradiation induced a type-1-interferon-associated inflammatory response in HUVECs involving IRF7 and its transcriptional targets, with the source data deposited in GEO under accession GSE76484.
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sections[0] "Abstract" paragraph 1
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The gene ontology analysis revealed that the down-regulated genes were associated with cell cycle regulation, whereas the up-regulated genes were associated with inflammatory responses, in particular, the type 1 interferon response.
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sections[0] "Abstract" paragraph 1
quote
The computational analysis using ingenuity pathway analysis also identified a gene network containing the interferon response factor 7 (IRF7) and its transcriptional targets such as interferon-induced transcripts (IFITs) and Mx1, which have been known to be associated with inflammation in endothelial cells.
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sections[0] "Abstract" paragraph 1
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The dataset is publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession number GSE76484.
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Global-scale microarray and computational gene-expression analysis showed that 2.5 Gy X-irradiation induced a type-1-interferon-associated inflammatory response in HUVECs involving IRF7 and its transcriptional targets, with the source data deposited in GEO under accession GSE76484.
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Expression data from human unbilical endothelial cells (HUVEC) irradiated with X-ray
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Table 2
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Expression levels of genes in the identified genetic network.
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202086_at
[1]
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[3]
252.4
[4]
286.3
[5]
246.8
[6]
629.3
[7]
− 0.09
[8]
0.09
[9]
− 0.12
[10]
1.23
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[0]
202307_s_at
[1]
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1.6
[3]
569.8
[4]
861.9
[5]
858.7
[6]
918.4
[7]
− 0.59
[8]
0
[9]
0
[10]
0.09
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[0]
202672_s_at
[1]
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[2]
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[3]
152
[4]
282.3
[5]
299.2
[6]
321.3
[7]
− 0.93
[8]
− 0.04
[9]
0.04
[10]
0.14
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[0]
203153_at
[1]
IFIT1
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250.7
[4]
403.1
[5]
168.7
[6]
686.4
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− 0.34
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0.34
[9]
− 0.91
[10]
1.11
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203945_at
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121.3
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147.6
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125.6
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185.8
[7]
− 0.17
[8]
0.12
[9]
− 0.12
[10]
0.45
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204415_at
[1]
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1.7
[3]
1314.2
[4]
1563.2
[5]
1417.6
[6]
2207.2
[7]
− 0.18
[8]
0.07
[9]
− 0.07
[10]
0.57
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[0]
204439_at
[1]
IFI44L
[2]
2.4
[3]
151.4
[4]
185.9
[5]
112.9
[6]
370.4
[7]
− 0.15
[8]
0.15
[9]
− 0.57
[10]
1.14
[8] array · 11 items
[0]
204698_at
[1]
ISG20
[2]
1.5
[3]
260
[4]
370.1
[5]
302.1
[6]
401
[7]
− 0.36
[8]
0.15
[9]
− 0.15
[10]
0.26
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[0]
206271_at
[1]
TLR3
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1.8
[3]
83.1
[4]
103.9
[5]
108
[6]
149.5
[7]
− 0.35
[8]
− 0.03
[9]
0.03
[10]
0.5
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[0]
207850_at
[1]
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[3]
124.3
[4]
179.7
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118.9
[6]
214.2
[7]
− 0.27
[8]
0.27
[9]
− 0.33
[10]
0.52
[11] array · 11 items
[0]
208436_s_at
[1]
IRF7
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2
[3]
342.2
[4]
551.1
[5]
558.2
[6]
687
[7]
− 0.7
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− 0.01
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0.01
[10]
0.31
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[0]
209941_at
[1]
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78
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152.2
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149.4
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− 0.95
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0.01
[9]
0.11
[10]
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213191_at
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243.4
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− 0.2
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0.38
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0.2
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214022_s_at
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526.9
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1167.5
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− 0.08
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0.08
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0.79
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215719_x_at
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313
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620.3
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510.1
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475.6
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0.33
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0.05
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226495_at
[1]
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1103.3
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1340.1
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1821.3
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0.02
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− 0.02
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0.46
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[0]
226603_at
[1]
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[3]
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788.5
[7]
− 0.18
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− 0.08
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0.08
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0.44
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226702_at
[1]
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127.6
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[10]
1.21
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226757_at
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146
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0.21
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0.38
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[0]
228617_at
[1]
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269.3
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560.3
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− 0.13
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0.13
[10]
0.93
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[0]
229450_at
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293.7
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399.5
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254.2
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603.4
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Table 3
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Top five upstream regulators and target molecules.
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Target molecules in dataset
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TLR3
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ARG2, ATF3, CMPK2,CXCL11, CXCL3, FAS, IFI44L, IFI6, IFIT1, IFIT2, IFIT3, IRF7, ISG15, ISG20, MX1, RIPK1, TICAM1, TLR3
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[0]
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4.24E-07
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CMPK2, IFI44L, IFI6, IFIT1, IFIT2, IFIT3, IFITM1, IRF7, ISG15, ISG20, MX1, SAMD9L, TAP1, XAF1
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TICAM1
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0.594
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1.60E-05
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[0]
PPARD
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Ligand-dependent nuclear receptor
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1.87E-03
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Principal component analysis (PCA), gene ontology (GO) analysis, and hierarchical clustering from the obtained normalized intensity data were performed using GeneSpring® software (Agilent).
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The dataset is publicly available at the Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) with accession number GSE76484.
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ing radiation, we carried out a global scale microarray and computational gene expression analyses o
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Table 1 Supplementary Fig. 1Verification of microarray results by real-time qPCR. HUVEC cells were
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s Cell culture and X-irradiation HUVECs were cultured in Humedia EB-2 (Wako), as previously described
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Principal component analysis (PCA), gene ontology (GO) analysis, and hierarchical clustering from the obtained normalized intensity data were performed using GeneSpring® software (Agilent).
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Complete file
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HUVEC cells were"], "order_basis": "paper_text_order:399", "id": "assay:1"}, {"role": "data_generation", "definition_id": "cell_culture", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.77, "evidence": ["s Cell culture and X-irradiation HUVECs were cultured in Humedia EB-2 (Wako), as previously described"], "order_basis": "paper_text_order:1546", "id": "assay:2"}, {"role": "data_generation", "definition_id": "qpcr", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["ification of microarray results by real-time qPCR. 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