Evidence map›Paper›PMID 21637828›Full record

ArticlePloS one2011

Deep sequencing reveals novel microRNAs and regulation of microRNA expression during cell senescence.

Joseph M Dhahbi, Hani Atamna, Dario Boffelli, Wendy Magis, Stephen R Spindler, David I K Martin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

55 citing papers in PubMed, 83 citations in OpenAlex.

  1. Trial
  2. Photodynamic Therapy Modulates pri-miRNA Expression inCurrent issues in molecular biology · 2025
    Article
  3. Article
  4. Identification of Oncogene-Induced Senescence-Associated MicroRNAs.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Deciphering the role of microRNAs in mustard gas-induced toxicity.Annals of the New York Academy of Sciences · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

6 authors at 2 institutions in 1 country.

Joseph M DhahbiCenter for Genetics, Children's Hospital Oakland Research Institute, Oakland, California, United States of America. jdhahbi@chori.org
Hani Atamna
Dario Boffelli
Wendy Magis
Stephen R Spindler
David I K Martin
University of California, Riverside · USCommonwealth Medical College · US

Funding

Identification of Primate-Specific Regulatory Elements of Cholesterol HomeostasisR01HL084474 · NHLBI · CHILDREN'S HOSPITAL & RES CTR AT OAKLAND · PI BOFFELLI, DARIO · 2007 to 2011
$2.0M
Epigenetic Suppression of the Obese Yellow PhenotypeR01CA115768 · NCI · CHILDREN'S HOSPITAL &RES CTR AT OAKLAND · PI MARTIN, DAVID IAN KINGSTON · 2005 to 2009
$1.5M
A high-throughput screen for candidate agents that may reverse gamma-globin silenR21DK080428 · NIDDK · CHILDREN'S HOSPITAL & RES CTR AT OAKLAND · PI MARTIN, DAVID IAN KINGSTON · 2009 to 2010
$440k
An Assay to Identify and Classify EpimutagensR21ES016581 · NIEHS · CHILDREN'S HOSPITAL & RES CTR AT OAKLAND · PI MARTIN, DAVID IAN KINGSTON · 2008 to 2009
$440k
NCI NIH HHS CA115768NCI NIH HHS R01 CA115768NHLBI NIH HHS HL084474NHLBI NIH HHS R01 HL084474NIDDK NIH HHS DK080428NIDDK NIH HHS R21 DK080428NIEHS NIH HHS ES016581NIEHS NIH HHS R21 ES016581
6 · The paper itself

Abstract

In cell senescence, cultured cells cease proliferating and acquire aberrant gene expression patterns. MicroRNAs (miRNAs) modulate gene expression through translational repression or mRNA degradation and have been implicated in senescence. We used deep sequencing to carry out a comprehensive survey of miRNA expression and involvement in cell senescence. Informatic analysis of small RNA sequence datasets from young and senescent IMR90 human fibroblasts identifies many miRNAs that are regulated (either up or down) with cell senescence. Comparison with mRNA expression profiles reveals potential mRNA targets of these senescence-regulated miRNAs. The target mRNAs are enriched for genes involved in biological processes associated with cell senescence. This result greatly extends existing information on the role of miRNAs in cell senescence and is consistent with miRNAs having a causal role in the process.

Indexed as

Gene Expression RegulationBiological PhenomenaCellular SenescenceCluster AnalysisDatabases, GeneticDown-RegulationFibroblastsGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansMicroRNAsMolecular Sequence AnnotationUp-RegulationMicroRNAs

Identifiers

PMID21637828
PMCPMC3102725
OpenAlexW2077997396

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.