Evidence map›Paper›PMID 26353930›Full record

ArticleOncotarget2015

H19 non coding RNA-derived miR-675 enhances tumorigenesis and metastasis of breast cancer cells by downregulating c-Cbl and Cbl-b.

Constance Vennin, Nathalie Spruyt, Fatima Dahmani, Sylvain Julien, François Bertucci, Pascal Finetti, Thierry Chassat, Roland P Bourette, Xuefen Le Bourhis, Eric Adriaenssens

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 3 pooled it
11.4field-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

123 citing papers in PubMed, 3 syntheses or guidelines pooled it, 197 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Cells · 2026
    Review
  6. Article
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  9. Article
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  11. Article
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  14. Article
  15. Review
  16. LncRNAs in oncogenic microenvironment: from threat to therapy.Frontiers in cell and developmental biology · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Long noncoding RNA (lncRNA)Genes & diseases · 2023
    Review

63 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

10 authors at 6 institutions in 1 country.

Constance VenninINSERM U908, Cell Plasticity and Cancer, F-59655, Villeneuve d'Ascq, France.
Nathalie SpruytCNRS UMR 8161, F-59021, Lille, France.
Fatima DahmaniCNRS UMR 8161, F-59021, Lille, France.
Sylvain JulienINSERM U908, Cell Plasticity and Cancer, F-59655, Villeneuve d'Ascq, France.
François BertucciPaoli-Calmettes Institute, Aix -Marseille University, F-13009, Marseille, France.
Pascal FinettiPaoli-Calmettes Institute, Aix -Marseille University, F-13009, Marseille, France.
Thierry ChassatPLETHA, Institut Pasteur Lille, F-59019, Lille, France.
Roland P BouretteCNRS UMR 8161, F-59021, Lille, France.
Xuefen Le BourhisINSERM U908, Cell Plasticity and Cancer, F-59655, Villeneuve d'Ascq, France.
Eric AdriaenssensINSERM U908, Cell Plasticity and Cancer, F-59655, Villeneuve d'Ascq, France.
Université de Lille · FRCentre National de la Recherche Scientifique · FRInserm · FRAix-Marseille Université · FRInstitut Paoli-Calmettes · FRInstitut Pasteur de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

H19 is a long non-coding RNA precursor of miR-675 microRNA. H19 is increasingly described to play key roles in the progression and metastasis of cancers from different tissue origins. We have previously shown that the H19 gene is activated by growth factors and increases breast cancer cell invasion. In this study, we established H19/miR-675 ectopic expression models of MDA-MB-231 breast cancer cells to further investigate the underlying mechanisms of H19 oncogenic action. We showed that overexpression of H19/miR-675 enhanced the aggressive phenotype of breast cancer cells including increased cell proliferation and migration in vitro, and increased tumor growth and metastasis in vivo. Moreover, we identified ubiquitin ligase E3 family (c-Cbl and Cbl-b) as direct targets of miR-675 in breast cancer cells. Using a luciferase assay, we demonstrated that H19, through its microRNA, decreased both c-Cbl and Cbl-b expression in all breast cancer cell lines tested. Thus, by directly binding c-Cbl and Cbl-b mRNA, miR-675 increased the stability and the activation of EGFR and c-Met, leading to sustained activation of Akt and Erk as well as enhanced cell proliferation and migration. Our data describe a novel mechanism of protumoral action of H19 in breast cancer.

Indexed as

Cell MovementAdaptor Proteins, Signal TransducingAnimalsBreast NeoplasmsCarcinogenesisCell ProliferationErbB ReceptorsExtracellular Signal-Regulated MAP KinasesFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsMice, SCIDMicroRNAsNeoplasm MetastasisPhenotypeAdaptor Proteins, Signal TransducingCBLB protein, humanCBL protein, humanEGFR protein, humanErbB ReceptorsExtracellular Signal-Regulated MAP KinasesH19 long non-coding RNAMicroRNAsMIRN675 microRNA, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-cblProto-Oncogene Proteins c-metRNA, Long NoncodingRNA, Messengerbreast cancerCBLH19miRNAtyrosine kinase receptor

Identifiers

PMID26353930
PMCPMC4745721
OpenAlexW2139766730

What OpenQuestion holds

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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.