Evidence map›Paper›PMID 24742936›Full record

ArticleRNA (New York, N.Y.)2014

miR-19b promotes tumor growth and metastasis via targeting TP53.

Yu Fan, Shenyi Yin, Yang Hao, Junyu Yang, Hanshuo Zhang, Changhong Sun, Ming Ma, Qing Chang, Jianzhong Jeff Xi

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Identification of Oncogene-Induced Senescence-Associated MicroRNAs.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  6. How MicroRNAs Command the Battle against Cancer.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Focus on the tumor microenvironment: A seedbed for neuroendocrine prostateFrontiers in cell and developmental biology · 2022
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

9 authors at 1 institution in 1 country.

Yu FanBiomedical Engineering Department, College of Engineering.
Shenyi YinBiomedical Engineering Department, College of Engineering.
Yang HaoBiomedical Engineering Department, College of Engineering.
Junyu YangBiomedical Engineering Department, College of Engineering.
Hanshuo ZhangBiomedical Engineering Department, College of Engineering.
Changhong SunBiomedical Engineering Department, College of Engineering.
Ming MaBiomedical Engineering Department, College of Engineering.
Qing ChangBiomedical Engineering Department, College of Engineering.
Jianzhong Jeff XiBiomedical Engineering Department, College of Engineering State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Molecular Medicine, Peking University, Beijing, 100871, China.
Peking University · CN

Funding

Ethanol induced brain injury is decreased by inhibiting TIEG2 mediated cell deathR01AA020103 · NIAAA · UNIVERSITY OF MISSISSIPPI MED CTR · PI WANG, JUNMING · 2011 to 2014
$1.4M
NIAAA NIH HHS R01 AA020103
6 · The paper itself

Abstract

Tumor suppressor TP53 (or p53) is one of the most important regulators in numerous physiological and pathological processes. Recently, the miRNA-mediated post-transcription regulation of p53 has been studied. However, systematic studies of miRNA targeting sites within the p53 gene are still a challenging task. Here, we developed a dual-color assay capable of identifying miRNA targeting sites in a certain gene, specifically p53, in a simple, direct, and robust manner. Results showed that p53 was a direct and critical target of miR-19b, but not miR-19a, regardless of sequence similarity. Overexpression of miR-19b observed in human cancer cells can diminish p53 protein levels and, subsequently, downstream components such as Bax and p21. This miR-19b-mediated p53 reduction was shown to promote cell cycle, cell migration or invasion, and repress senescence and apoptosis in vitro. Further investigation revealed that miR-19b controls tumor growth and metastasis in vivo. Therefore, it is possible that miR-19b antagomirs or sponges could be developed as therapeutic agents against tumor development.

Indexed as

Apoptosisbcl-2-Associated X ProteinCell CycleCell LineCell Line, TumorCell MovementCyclin-Dependent Kinase Inhibitor p21Down-RegulationGenes, p53HEK293 CellsHeLa CellsHumansMCF-7 CellsMicroRNAsNeoplasm MetastasisTumor Suppressor Protein p53BAX protein, humanbcl-2-Associated X ProteinCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21MicroRNAsMIRN19A microRNA, humanTumor Suppressor Protein p53miRNATP53tumor metastasis

Identifiers

PMID24742936
PMCPMC4024631
OpenAlexW2167430092

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.