Evidence map›Paper›PMID 21468029›Full record

ArticleThe EMBO journal2011

microRNA-214 contributes to melanoma tumour progression through suppression of TFAP2C.

Elisa Penna, Francesca Orso, Daniela Cimino, Enrico Tenaglia, Antonio Lembo, Elena Quaglino, Laura Poliseno, Adele Haimovic, Simona Osella-Abate, Cristiano De Pittà and 6 more

Abstract read
In one paragraph

Article in The EMBO journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 1 pooled it
11.8field-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

138 citing papers in PubMed, 1 synthesis or guideline pooled it, 262 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The miR-214-3p/Biology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. The chimeric aptamer axl-miR-214sponge inhibits breast cancer and melanoma dissemination.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  8. Differential miRNA signatures in Hepatitis E Virus Infection: Insights into acute, chronic, and pregnancy-related outcomes.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Review
  9. Review
  10. Article
  11. A New Approach to Melanoma Treatment: microRNAs.Current topics in medicinal chemistry · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Stroma-derived miR-214 coordinates tumor dissemination.Journal of experimental & clinical cancer research : CR · 2023
    Article
  16. Role of miRNA in Melanoma Development and Progression.International journal of molecular sciences · 2022
    Review
  17. Article
  18. Review
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 3 countries.

Elisa PennaMolecular Biotechnology Center (MBC), University of Torino, Torino, Italy.
Francesca Orso
Daniela Cimino
Enrico Tenaglia
Antonio Lembo
Elena Quaglino
Laura Poliseno
Adele Haimovic
Simona Osella-Abate
Cristiano De Pittà
Eva Pinatel
Michael B Stadler
Paolo Provero
Maria Grazia Bernengo
Iman Osman
Daniela Taverna
University of Turin · ITColumbia University Irving Medical Center · USTorino e-district · IT5T Torino (Italy) · ITFriedrich Miescher Institute · CHUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma is fatal in its metastatic stage. It is therefore essential to unravel the molecular mechanisms that govern disease progression to metastasis. MicroRNAs (miRs) are endogenous non-coding RNAs involved in tumourigenesis. Using a melanoma progression model, we identified a novel pathway controlled by miR-214 that coordinates metastatic capability. Pathway components include TFAP2C, homologue of a well-established melanoma tumour suppressor, the adhesion receptor ITGA3 and multiple surface molecules. Modulation of miR-214 influences in vitro tumour cell movement and survival to anoikis as well as extravasation from blood vessels and lung metastasis formation in vivo. Considering that miR-214 is known to be highly expressed in human melanomas, our data suggest a critical role for this miRNA in disease progression and the establishment of distant metastases.

Indexed as

Gene Expression RegulationAnimalsCell MovementCell ProliferationCells, CulturedCell SurvivalHumansIntegrinsLungLung NeoplasmsMelanomaMiceMicroRNAsNeoplasm MetastasisTranscription Factor AP-2IntegrinsMicroRNAsMIRN214 microRNA, humanTFAP2C protein, humanTranscription Factor AP-2

Identifiers

PMID21468029
PMCPMC3098476
OpenAlexW2098302826

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.