Evidence map›Paper›PMID 35053470›Full record

ArticleCancers2022

PRMT1 Regulates EGFR and Wnt Signaling Pathways and Is a Promising Target for Combinatorial Treatment of Breast Cancer.

Samyuktha Suresh, Solène Huard, Amélie Brisson, Fariba Némati, Rayan Dakroub, Coralie Poulard, Mengliang Ye, Elise Martel, Cécile Reyes, David C Silvestre and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
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  8. Review
  9. Article
  10. Article
  11. Role of PRMT1 and PRMT5 in Breast Cancer.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Review
  14. Role of EGFR and FASN in breast cancer progression.Journal of cell communication and signaling · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Hypoxia-Induced FUS-circTBC1D14 Stress Granules Promote Autophagy in TNBC.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  20. Article
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

18 authors at 4 institutions in 2 countries.

Samyuktha SureshBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.ORCID 0000-0001-8261-4097
Solène HuardBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Amélie BrissonBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Fariba NématiPre-Clinical Investigation Laboratory, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Rayan DakroubBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Coralie PoulardCancer Research Center of Lyon, CNRS UMR5286, Inserm U1052, University of Lyon, 69000 Lyon, France.
Mengliang YeBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Elise MartelPlatform of Experimental Pathology, Department of Diagnostic and Theranostic Medicine, Institut Curie-Hospital, 75005 Paris, France.
Cécile ReyesGenomics Core Facility, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
David C SilvestreBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Didier MeseurePlatform of Experimental Pathology, Department of Diagnostic and Theranostic Medicine, Institut Curie-Hospital, 75005 Paris, France.
André NicolasPlatform of Experimental Pathology, Department of Diagnostic and Theranostic Medicine, Institut Curie-Hospital, 75005 Paris, France.
David GentienGenomics Core Facility, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.ORCID 0000-0001-8317-5188
Hussein Fayyad-KazanLaboratory of Cancer Biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath, Beirut 1003, Lebanon.
Muriel Le RomancerCancer Research Center of Lyon, CNRS UMR5286, Inserm U1052, University of Lyon, 69000 Lyon, France.ORCID 0000-0002-8491-4015
Didier DecaudinPre-Clinical Investigation Laboratory, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Sergio Roman-RomanTranslational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.
Thierry DuboisBreast Cancer Biology Group, Translational Research Department, Institut Curie-PSL Research University, 75005 Paris, France.ORCID 0000-0003-4739-6164
Université Paris Sciences et Lettres · FRInstitut Curie · FRLebanese University · LBUniversité Claude Bernard Lyon 1 · FR

Funding

European Union's Horizon 2020 Research and Innovation Programme Marie Skłodowska-Curie grant agreement No 666003Fondation ARC pour la recherche sur le cancer NAFrench Embassy and the Lebanese University, Safar Volet 1 NAInstitut de Recherches Servier NAInstitute Curie NALa Ligue contre le Cancer NA
6 · The paper itself

Abstract

Identifying new therapeutic strategies for triple-negative breast cancer (TNBC) patients is a priority as these patients are highly prone to relapse after chemotherapy. Here, we found that protein arginine methyltransferase 1 (PRMT1) is highly expressed in all breast cancer subtypes. PRMT1 depletion decreases cell survival by inducing DNA damage and apoptosis in various breast cancer cell lines. Transcriptomic analysis and chromatin immunoprecipitation revealed that PRMT1 regulates the epidermal growth factor receptor (EGFR) and the Wnt signaling pathways, reported to be activated in TNBC. PRMT1 enzymatic activity is also required to stimulate the canonical Wnt pathway. Type I PRMT inhibitors decrease breast cancer cell proliferation and show anti-tumor activity in a TNBC xenograft model. These inhibitors display synergistic interactions with some chemotherapies used to treat TNBC patients as well as erlotinib, an EGFR inhibitor. Therefore, targeting PRMT1 in combination with these chemotherapies may improve existing treatments for TNBC patients.

Indexed as

breast cancerdrug combinationsEGFRPRMT1Wnt signaling

Identifiers

PMID35053470
PMCPMC8774276
OpenAlexW4226337134

What OpenQuestion holds

Textmetadata
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.