Evidence map›Paper›PMID 22459148›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2012

MicroRNA-224 is up-regulated in hepatocellular carcinoma through epigenetic mechanisms.

Yu Wang, Han Chong Toh, Pierce Chow, Alexander Y F Chung, David J Meyers, Philip A Cole, London L P J Ooi, Caroline G L Lee

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 112 citations in OpenAlex.

  1. Review
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  5. Article
  6. Review
  7. Review
  8. The Emerging Role of Stress Granules in Hepatocellular Carcinoma.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. MicroRNA 452 regulatesJournal of genetics · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

5 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 6 institutions in 2 countries.

Yu WangDepartment of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Han Chong Toh
Pierce Chow
Alexander Y F Chung
David J Meyers
Philip A Cole
London L P J Ooi
Caroline G L Lee
National Cancer Centre Singapore · SGSingapore General Hospital · SGDuke-NUS Medical School · SGJohns Hopkins Medicine · USJohns Hopkins University · USNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA-224 (miR-224) is one of the most commonly up-regulated microRNAs in hepatocellular carcinoma (HCC), which affects crucial cellular processes such as apoptosis and cell proliferation. In this study, we aim to elucidate the molecular mechanism that leads to the overexpression of miR-224 in HCC. We examined the transcript expression of miR-224 and neighboring miR-452 and genes on chromosome Xq28 in tumor and paired adjacent nontumorous tissues from 100 patients with HCC and found that miR-224 is coordinately up-regulated with its neighboring microRNA (miRNA) and genes. This coordinated up-regulation of miRNAs and genes at the Xq28 locus can be mimicked in nontransformed immortalized human liver cells by the introduction of histone deacetylase (HDAC) inhibitors, which resulted in a corresponding increase in histone H3 acetylation in this region. This miR-224-residing locus in Xq28 is reciprocally regulated by HDAC1, HDAC3, and histone acetylase protein, E1A binding protein p300 (EP300). Notably, in HCC tumors that significantly overexpress microRNA-224, EP300 is also overexpressed and displays increased binding to the Xq28 locus. In transformed HCC cells, high miR-224 expression can be attenuated through the inhibition of EP300, using either siRNA or the specific drug C646. In summary, overexpression of EP300 may account, in part, for the up-regulation of miR-224 expression in patients with HCC.

Indexed as

AcetylationBase SequenceBiomarkers, TumorCarcinoma, HepatocellularChromosomes, Human, XDNA PrimersE1A-Associated p300 ProteinEpigenesis, GeneticHep G2 CellsHistone Deacetylase 1Histone Deacetylase 3Histone DeacetylasesHistonesHumansLiver NeoplasmsMicroRNAsBiomarkers, TumorDNA PrimersE1A-Associated p300 ProteinEP300 protein, humanHDAC1 protein, humanHistone Deacetylase 1Histone Deacetylase 3Histone DeacetylasesHistonesMicroRNAsMIRN224 microRNA, humanMIRN452 microRNA, humanRNA, NeoplasmRNA, Small Interfering

Identifiers

PMID22459148
PMCPMC3382089
OpenAlexW2141616427

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.