Evidence map›Paper›PMID 20509943›Full record

ArticleBMC genomics2010

Bioinformatic identification and characterization of human endothelial cell-restricted genes.

Manoj Bhasin, Lei Yuan, Derin B Keskin, Hasan H Otu, Towia A Libermann, Peter Oettgen

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 64 citations in OpenAlex.

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  9. The secretome mouse provides a genetic platform to delineate tissue-specific in vivo secretion.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  12. The in vivo endothelial cell translatome is highly heterogeneous across vascular beds.Proceedings of the National Academy of Sciences of the United States of America · 2019
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  14. Comparative Transcriptomics ofJACC. Basic to translational science · 2019
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  19. Endothelial Cell Aging: How miRNAs Contribute?Journal of clinical medicine · 2018
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Manoj BhasinDivision of Interdisciplinary Medicine and Biotechnology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Lei Yuan
Derin B Keskin
Hasan H Otu
Towia A Libermann
Peter Oettgen
Harvard University · USBeth Israel Deaconess Medical Center · USDana-Farber Cancer Institute · US

Funding

VASCULAR TOPOGRAPHY OF CD39/NTPDASESP01HL076540 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI AIRD, WILLIAM C · 2004 to 2014
$20.3M
Regulation of Vascular Inflammation by ESE-1R01HL067219 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI OETTGEN, J PETER PETER · 2001 to 2004
$1.4M
NHLBI NIH HHS HL-67219NHLBI NIH HHS P01 HL76540
6 · The paper itself

Abstract

backgroundIn this study, we used a systematic bioinformatics analysis approach to elucidate genes that exhibit an endothelial cell (EC) restricted expression pattern, and began to define their regulation, tissue distribution, and potential biological role.

resultsUsing a high throughput microarray platform, a primary set of 1,191 transcripts that are enriched in different primary ECs compared to non-ECs was identified (LCB >3, FDR <2%). Further refinement of this initial subset of transcripts, using published data, yielded 152 transcripts (representing 109 genes) with different degrees of EC-specificity. Several interesting patterns emerged among these genes: some were expressed in all ECs and several were restricted to microvascular ECs. Pathway analysis and gene ontology demonstrated that several of the identified genes are known to be involved in vasculature development, angiogenesis, and endothelial function (P < 0.01). These genes are enriched in cardiovascular diseases, hemorrhage and ischemia gene sets (P < 0.001). Most of the identified genes are ubiquitously expressed in many different tissues. Analysis of the proximal promoter revealed the enrichment of conserved binding sites for 26 different transcription factors and analysis of the untranslated regions suggests that a subset of the EC-restricted genes are targets of 15 microRNAs. While many of the identified genes are known for their regulatory role in ECs, we have also identified several novel EC-restricted genes, the function of which have yet to be fully defined.

conclusionThe study provides an initial catalogue of EC-restricted genes most of which are ubiquitously expressed in different endothelial cells.

Indexed as

Computational BiologyGenesBinding SitesCell DifferentiationCell LineDiseaseEndothelial CellsGene Expression ProfilingHumansMicroRNAsNeovascularization, PhysiologicOrgan SpecificityRegulatory Sequences, Nucleic AcidTranscription FactorsMicroRNAsTranscription Factors

Identifiers

PMID20509943
PMCPMC2887814
OpenAlexW2120004578

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.