Evidence map›Paper›PMID 28652379›Full record

ArticleEMBO reports2017

The mutant p53-ID4 complex controls VEGFA isoforms by recruiting lncRNA MALAT1.

Magdalena Pruszko, Elisa Milano, Mattia Forcato, Sara Donzelli, Federica Ganci, Silvia Di Agostino, Simone De Panfilis, Francesco Fazi, David O Bates, Silvio Bicciato and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
4.2field-weighted citation impact, top 4% 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

77 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. SR proteins in cancer: function, regulation, and small inhibitor.Cellular & molecular biology letters · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 5 countries.

Magdalena PruszkoDepartment of Molecular Biology, International Institute of Molecular and Cell Biology in Warsaw, Warsaw, Poland.
Elisa MilanoOncogenomic and Epigenetic Unit, Italian National Cancer Institute "Regina Elena", Rome, Italy.ORCID 0000-0003-0579-7592
Mattia ForcatoDepartment of Life Sciences, Center for Genome Research, University of Modena and Reggio Emilia, Modena, Italy.
Sara DonzelliOncogenomic and Epigenetic Unit, Italian National Cancer Institute "Regina Elena", Rome, Italy.
Federica GanciOncogenomic and Epigenetic Unit, Italian National Cancer Institute "Regina Elena", Rome, Italy.
Silvia Di AgostinoOncogenomic and Epigenetic Unit, Italian National Cancer Institute "Regina Elena", Rome, Italy.ORCID 0000-0003-3730-1125
Simone De PanfilisCentre for Life Nano Science, Istituto Italiano di Tecnologia, Rome, Italy.
Francesco FaziDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, Rome, Italy.
David O BatesDivision of Cancer and Stem Cells, Cancer Biology, School of Medicine, Queen's Medical Centre, University of Nottingham, Nottingham, UK.
Silvio BicciatoDepartment of Life Sciences, Center for Genome Research, University of Modena and Reggio Emilia, Modena, Italy.
Maciej ZyliczDepartment of Molecular Biology, International Institute of Molecular and Cell Biology in Warsaw, Warsaw, Poland.
Alicja ZyliczDepartment of Molecular Biology, International Institute of Molecular and Cell Biology in Warsaw, Warsaw, Poland.
Giovanni BlandinoOncogenomic and Epigenetic Unit, Italian National Cancer Institute "Regina Elena", Rome, Italy giovanni.blandino@ifo.gov.it giulia.fontemaggi@ifo.gov.it.ORCID 0000-0002-6970-2241
Giulia FontemaggiOncogenomic and Epigenetic Unit, Italian National Cancer Institute "Regina Elena", Rome, Italy giovanni.blandino@ifo.gov.it giulia.fontemaggi@ifo.gov.it.ORCID 0000-0001-8332-8842
National Cancer Institute · MYInternational Institute of Molecular and Cell Biology · PLUniversity of Modena and Reggio Emilia · ITItalian Institute of Technology · ITSapienza University of Rome · ITUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The abundant, nuclear-retained, metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) has been associated with a poorly differentiated and aggressive phenotype of mammary carcinomas. This long non-coding RNA (lncRNA) localizes to nuclear speckles, where it interacts with a subset of splicing factors and modulates their activity. In this study, we demonstrate that oncogenic splicing factor SRSF1 bridges MALAT1 to mutant p53 and ID4 proteins in breast cancer cells. Mutant p53 and ID4 delocalize MALAT1 from nuclear speckles and favor its association with chromatin. This enables aberrant recruitment of MALAT1 on VEGFA pre-mRNA and modulation of VEGFA isoforms expression. Interestingly, VEGFA-dependent expression signatures associate with ID4 expression specifically in basal-like breast cancers carrying

Indexed as

Breast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansInhibitor of Differentiation ProteinsMutationNeovascularization, PathologicProtein IsoformsRNA, Long NoncodingRNA SplicingSerine-Arginine Splicing FactorsTumor Suppressor Protein p53Vascular Endothelial Growth Factor AID4 protein, humanInhibitor of Differentiation ProteinsMALAT1 long non-coding RNA, humanProtein IsoformsRNA, Long NoncodingSerine-Arginine Splicing FactorsSRSF1 protein, humanTP53 protein, humanTumor Suppressor Protein p53Vascular Endothelial Growth Factor AVEGFA protein, humanID4MALAT1mutant p53SRSF1VEGFA

Identifiers

PMID28652379
PMCPMC5538427
OpenAlexW2708207694

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.