Evidence map›Paper›PMID 31569512›Full record

ReviewCancers2019

José L Marín-Rubio, Laura Vela-Martín, José Fernández-Piqueras, María Villa-Morales

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  9. Article
  10. Review
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  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. FADD as a key molecular player in cancer progression.Molecular medicine (Cambridge, Mass.) · 2022
    Review
  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

4 authors at 3 institutions in 2 countries.

José L Marín-RubioInstitute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne NE2 4HH, UK. Jose.Marin-Rubio@newcastle.ac.uk.ORCID 0000-0002-7682-0190
Laura Vela-MartínDepartamento de Biología, Universidad Autónoma de Madrid, 28049 Madrid, Spain. laura.velam@estudiante.uam.es.
José Fernández-PiquerasDepartamento de Biología, Universidad Autónoma de Madrid, 28049 Madrid, Spain. jfpiqueras@cbm.csic.es.ORCID 0000-0003-4520-6785
María Villa-MoralesDepartamento de Biología, Universidad Autónoma de Madrid, 28049 Madrid, Spain. maria.villa@uam.es.ORCID 0000-0001-7906-0169
Centre for Biomedical Network Research on Rare Diseases · ESCentro de Biología Molecular Severo Ochoa · ESNewcastle University · GB

Funding

Consejería de Sanidad, Comunidad de Madrid B2017/BMD-3778 LINFOMAS-CMFundación Banco Santander Institutional grantFundación Científica Asociación Española Contra el Cáncer AECC 2018 PROYE18054PIRIFundación Ramón Areces Medicina de precisión y cáncerInstituto de Salud Carlos III ACCI-CIBERER-17 ISCIIIMinisterio de Economía y Competitividad BES-2013-065740Ministerio de Economía y Competitividad RTI2018-093330-B-I00Universidad Autónoma de Madrid Grants for Master Final Dissertation
6 · The paper itself

Abstract

FADD was initially described as an adaptor molecule for death receptor-mediated apoptosis, but subsequently it has been implicated in nonapoptotic cellular processes such as proliferation and cell cycle control. During the last decade, FADD has been shown to play a pivotal role in most of the signalosome complexes, such as the necroptosome and the inflammasome. Interestingly, various mechanisms involved in regulating FADD functions have been identified, essentially posttranslational modifications and secretion. All these aspects have been thoroughly addressed in previous reviews. However, FADD implication in cancer is complex, due to pleiotropic effects. It has been reported either as anti- or protumorigenic, depending on the cell type. Regulation of

Indexed as

chromosomal alterationsclinical implicationsepigenetic regulationFADDgene expressionmetabolismmutationspolymorphismsposttranslational modificationstranscription factors

Identifiers

PMID31569512
PMCPMC6826683
OpenAlexW2975808192

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.