Evidence map›Paper›PMID 25719243›Full record

ArticleCell death & disease2015

The calcineurin/NFAT pathway is activated in diagnostic breast cancer cases and is essential to survival and metastasis of mammary cancer cells.

C Tran Quang, S Leboucher, D Passaro, L Fuhrmann, M Nourieh, A Vincent-Salomon, J Ghysdael

Abstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

70 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Identification of Key Transcription Factors Associated with Lung Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Pooled it
  2. Trial
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  9. Calcineurin-mediated dephosphorylation stabilizes E2F1 protein by suppressing binding of the FBXW7 ubiquitin ligase subunit.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Tumor-Intrinsic Galectin-3 Suppresses Melanoma Metastasis.The Journal of investigative dermatology · 2024
    Article
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  16. LowJournal of Cancer · 2023
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10 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

7 authors.

C Tran Quang1] U1005-UMR3306-, Institut Curie, Bat 110 Centre Universitaire, Orsay 91405, France [2] Institut National de la Recherche Santé et de la Recherche Medicale, Orsay U1005, France [3] Centre National de la Recherche Scientifique, Orsay UMR3306, France.
S Leboucher1] U1005-UMR3306-, Institut Curie, Bat 110 Centre Universitaire, Orsay 91405, France [2] Institut National de la Recherche Santé et de la Recherche Medicale, Orsay U1005, France [3] Centre National de la Recherche Scientifique, Orsay UMR3306, France.
D Passaro1] U1005-UMR3306-, Institut Curie, Bat 110 Centre Universitaire, Orsay 91405, France [2] Institut National de la Recherche Santé et de la Recherche Medicale, Orsay U1005, France [3] Centre National de la Recherche Scientifique, Orsay UMR3306, France.
L Fuhrmann1] Centre de Recherche, Institut Curie, Paris 75005, France [2] CNRS UMR144, Paris 75005, France [3] Department of Biopathology, Institut Curie, Paris 75005, France.
M Nourieh1] Centre de Recherche, Institut Curie, Paris 75005, France [2] Department of Biopathology, Institut Curie, Paris 75005, France.
A Vincent-Salomon1] Centre de Recherche, Institut Curie, Paris 75005, France [2] Department of Biopathology, Institut Curie, Paris 75005, France [3] INSERM U934, Paris 75005, France.
J Ghysdael1] U1005-UMR3306-, Institut Curie, Bat 110 Centre Universitaire, Orsay 91405, France [2] Institut National de la Recherche Santé et de la Recherche Medicale, Orsay U1005, France [3] Centre National de la Recherche Scientifique, Orsay UMR3306, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear factor of activated T cells 1 (NFAT1) expression has been associated with increased migratory/invasive properties of mammary tumor-derived cell lines in vitro. It is unknown, however, if NFAT activation actually occurs in breast cancer cases and whether the calcineurin/NFAT pathway is important to mammary tumorigenesis. Using a cohort of 321 diagnostic cases of the major subgroup of breast cancer, we found Cn/NFAT pathway activated in ER(-)PR(-)HER2(-) triple-negative breast cancer subtype, whereas its prevalence is less in other subgroups. Using a small hairpin RNA-based gene expression silencing approach in murine mammary tumor cell line (4T1), we show that not only NFAT1 but also NFAT2 and their upstream activator Cn are essential to the migratory and invasive properties of mammary tumor cells. We also demonstrate that Cn, NFAT1 and NFAT2 are essential to the tumorigenic and metastatic properties of these cells in mice, a phenotype which coincides with increased apoptosis in vivo. Finally, global gene expression analyses identified several NFAT-deregulated genes, many of them being previously associated with mammary tumorigenesis. In particular, we identified the gene encoding a disintegrin and metalloproteinase with thrombonspondin motifs 1, as being a potential direct target of NFAT1. Thus, our results show that the Cn/NFAT pathway is activated in diagnostic cases of breast cancers and is essential to the tumorigenic and metastatic potential of mammary tumor cell line. These results suggest that pharmacological inhibition of the Cn/NFAT pathway at different levels could be of therapeutical interest for breast cancer patients.

Indexed as

AnimalsBreast NeoplasmsCalcineurinCell Line, TumorCell MovementFemaleMiceNFATC Transcription FactorsSignal TransductionTriple Negative Breast NeoplasmsCalcineurinNfatc1 protein, mouseNfatc2 protein, mouseNFATC Transcription Factors

Identifiers

PMID25719243
PMCPMC4669815

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Registered trials

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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.