Evidence map›Paper›PMID 29147069›Full record

ArticleMediators of inflammation2017

Expression Profiling of Long Noncoding RNA Splice Variants in Human Microvascular Endothelial Cells: Lipopolysaccharide Effects

Imran H Chowdhury, Hema P Narra, Abha Sahni, Kamil Khanipov, Casey L C Schroeder, Jignesh Patel, Yuriy Fofanov, Sanjeev K Sahni

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Long Noncoding RNA: Regulatory Mechanisms and Therapeutic Potential in Sepsis.Frontiers in cellular and infection microbiology · 2021
    Review
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  11. Review
  12. Article
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  14. Article
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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

8 authors at 1 institution in 1 country.

Imran H ChowdhuryDepartment of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.
Hema P NarraDepartment of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.
Abha SahniDepartment of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.
Kamil KhanipovDepartment of Pharmacology, University of Texas Medical Branch, Galveston, TX, USA.ORCID 0000-0002-3881-737X
Casey L C SchroederDepartment of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.
Jignesh PatelDepartment of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.
Yuriy FofanovDepartment of Pharmacology, University of Texas Medical Branch, Galveston, TX, USA.
Sanjeev K SahniDepartment of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.ORCID 0000-0001-7715-3652
The University of Texas Medical Branch at Galveston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial cell interactions with lipopolysaccharide (LPS) involve both activating and repressing signals resulting in pronounced alterations in their transcriptome and proteome. Noncoding RNAs are now appreciated as posttranscriptional and translational regulators of cellular signaling and responses, but their expression status and roles during endothelial interactions with LPS are not well understood. We report on the expression profile of long noncoding (lnc) RNAs of human microvascular endothelial cells in response to LPS. We have identified a total of 10,781 and 8310 lncRNA transcripts displaying either positive or negative regulation of expression, respectively, at 3 and 24 h posttreatment. A majority of LPS-induced lncRNAs are multiexonic and distributed across the genome as evidenced by their presence on all chromosomes. Present among these are a total of 44 lncRNAs with known regulatory functions, of which 41 multiexonic lncRNAs have multiple splice variants. We have further validated splice variant-specific expression of EGO (NONHSAT087634) and HOTAIRM1 (NONHSAT119666) at 3 h and significant upregulation of lnc-IL7R at 24 h. This study illustrates the genome-wide regulation of endothelial lncRNA splice variants in response to LPS and provides a foundation for further investigations of differentially expressed lncRNA transcripts in endothelial responses to LPS and pathophysiology of sepsis/septic shock.

Indexed as

Endothelial CellsGene Expression RegulationHumansLipopolysaccharidesRNA, Long NoncodingLipopolysaccharidesRNA, Long Noncoding

Identifiers

PMID29147069
PMCPMC5632992
OpenAlexW2760130693

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.