Evidence map›Paper›PMID 34576182›Full record

ReviewInternational journal of molecular sciences2021

C3G Protein, a New Player in Glioblastoma.

Sara Manzano, Alvaro Gutierrez-Uzquiza, Paloma Bragado, Angel M Cuesta, Carmen Guerrero, Almudena Porras

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. New and Old Key Players in Liver Cancer.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. 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

6 authors at 2 institutions in 1 country.

Sara ManzanoDepartamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain.ORCID 0000-0002-0052-511X
Alvaro Gutierrez-UzquizaDepartamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain.ORCID 0000-0002-0446-4131
Paloma BragadoDepartamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain.
Angel M CuestaDepartamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain.ORCID 0000-0002-6596-9600
Carmen GuerreroInstituto de Biología Molecular y Celular del Cáncer (IMBCC), Universidad de Salamanca-(CSIC), 37007 Salamanca, Spain.ORCID 0000-0002-8747-6831
Almudena PorrasDepartamento de Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad Complutense de Madrid (UCM), 28040 Madrid, Spain.ORCID 0000-0002-6495-3308
Universidad Complutense de Madrid · ESUniversidad de Salamanca · ES

Funding

Comunidad de Madrid MRF 2017-T1/BMD-5468Junta de Castilla y León SA078P20Ministerio de Ciencia e Innovación PID2019-104143RB-C21Ministerio de Ciencia e Innovación PID2019-104143RB-C22Ministerio de Ciencia e Innovación PID2019-104991RB-I00Ministerio de Economía y Competitividad SAF2016-76588-C2-1-RMinisterio de Economía y Competitividad SAF2016-76588-C2-2-R
6 · The paper itself

Abstract

C3G (RAPGEF1) is a guanine nucleotide exchange factor (GEF) for GTPases from the Ras superfamily, mainly Rap1, although it also acts through GEF-independent mechanisms. C3G regulates several cellular functions. It is expressed at relatively high levels in specific brain areas, playing important roles during embryonic development. Recent studies have uncovered different roles for C3G in cancer that are likely to depend on cell context, tumour type, and stage. However, its role in brain tumours remained unknown until very recently. We found that C3G expression is downregulated in GBM, which promotes the acquisition of a more mesenchymal phenotype, enhancing migration and invasion, but not proliferation. ERKs hyperactivation, likely induced by FGFR1, is responsible for this pro-invasive effect detected in

Indexed as

AnimalsGlioblastomaGuanine Nucleotide-Releasing Factor 2HumansNeoplastic Cells, Circulatingrap1 GTP-Binding ProteinsGuanine Nucleotide-Releasing Factor 2rap1 GTP-Binding ProteinsC3GglioblastomaRap

Identifiers

PMID34576182
PMCPMC8466177
OpenAlexW3199150205

What Socratic 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 Socratic graph.