Evidence map›Paper›PMID 18367535›Full record

ArticleJournal of virology2008

MicroRNA-155 is an Epstein-Barr virus-induced gene that modulates Epstein-Barr virus-regulated gene expression pathways.

Qinyan Yin, Jane McBride, Claire Fewell, Michelle Lacey, Xia Wang, Zhen Lin, Jennifer Cameron, Erik K Flemington

Abstract read
In one paragraph

Article in Journal of virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 262 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Review
  5. Article
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  7. Shaping the host cell environment with viral noncoding RNAs.Seminars in cell & developmental biology · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. A virus-induced circular RNA maintains latent infection of Kaposi's sarcoma herpesvirus.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Article
  13. Effects of aneuploidy on cell behaviour and function.Nature reviews. Molecular cell biology · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

86 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Qinyan YinLouisiana Cancer Research Consortium, New Orleans, USA.
Jane McBride
Claire Fewell
Michelle Lacey
Xia Wang
Zhen Lin
Jennifer Cameron
Erik K Flemington
Louisiana Cancer Research Center · USTulane University · US

Funding

UNCOVERING THE MECHANISMS OF OSTEOSARCOMA METASTASIS SUPPRESSION BY MTBPP20RR020152 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI PURSELL, ZACHARY F · 2004 to 2011
$17.0M
EBV BZLF1 GENE PRODUCTR01GM048045 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 1998 to 2007
$1.9M
Regulation of Epstein Barr virus reactivation through the co-activators, CBP/p300R01CA124311 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 2007 to 2011
$1.3M
Analysis of EBNA1 siRNA for inhibiting NPC tumor growthR21DE017008 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI FLEMINGTON, ERIK K · 2005 to 2006
$497k
NCI NIH HHS R01 CA124311NCRR NIH HHS P20 RR020152NIDCR NIH HHS R21 DE017008NIDCR NIH HHS R21-DE17008NIGMS NIH HHS R01 GM048045NIGMS NIH HHS R01-GM48045
6 · The paper itself

Abstract

The cellular microRNA miR-155 has been shown to be involved in lymphocyte activation and is expressed in Epstein-Barr virus (EBV)-infected cells displaying type III latency gene expression but not type I latency gene expression. We show here that the elevated levels of miR-155 in type III latency cells is due to EBV gene expression and not epigenetic differences in cell lines tested, and we show that expression in EBV-infected cells requires a conserved AP-1 element in the miR-155 promoter. Gene expression analysis was carried out in a type I latency cell line transduced with an miR-155-expressing retrovirus. This analysis identified both miR-155-suppressed and -induced cellular mRNAs and suggested that in addition to direct targeting of 3' untranslated regions (UTRs), miR-155 alters gene expression in part through the alteration of signal transduction pathways. 3' UTR reporter analysis of predicted miR-155 target genes identified the transcriptional regulatory genes encoding BACH1, ZIC3, HIVEP2, CEBPB, ZNF652, ARID2, and SMAD5 as miR-155 targets. Western blot analysis of the most highly suppressed of these, BACH1, showed lower expression in cells transduced with a miR-155 retrovirus. Inspection of the promoters from genes regulated in EBV-infected cells and in cells infected with an miR-155 retrovirus identified potential binding sequences for BACH1 and ZIC3. Together, these experiments suggest that the induction of miR-155 by EBV contributes to EBV-mediated signaling in part through the modulation of transcriptional regulatory factors.

Indexed as

AnimalsBase SequenceCell LineGene Expression RegulationHerpesvirus 4, HumanMiceMicroRNAsMolecular Sequence DataSignal TransductionTranscription Factor AP-1Transcription, GeneticMicroRNAsTranscription Factor AP-1

Identifiers

PMID18367535
PMCPMC2395216
OpenAlexW2166540695

What OpenQuestion holds

Textmetadata
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.