Evidence map›Paper›PMID 32351958›Full record

ArticleFrontiers in cell and developmental biology2020

Computational and

Nazareno González, Georgina A Cardama, Patricio Chinestrad, Javier Robles-Valero, Sonia Rodríguez-Fdez, L Francisco Lorenzo-Martín, Xosé R Bustelo, Pablo Lorenzano Menna, Daniel E Gomez

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Biomedicines · 2022
    Article
  9. Rac1, A Potential Target for Tumor Therapy.Frontiers in oncology · 2021
    Review
  10. 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

9 authors at 3 institutions in 2 countries.

Nazareno GonzálezLaboratory of Molecular Oncology, National University of Quilmes, Bernal, Argentina.
Georgina A CardamaLaboratory of Molecular Oncology, National University of Quilmes, Bernal, Argentina.
Patricio ChinestradMolecular Pharmacology Laboratory, National University of Quilmes, Bernal, Argentina.
Javier Robles-ValeroCentro de Investigación del Cáncer, CSIC-University of Salamanca, Salamanca, Spain.
Sonia Rodríguez-FdezCentro de Investigación del Cáncer, CSIC-University of Salamanca, Salamanca, Spain.
L Francisco Lorenzo-MartínCentro de Investigación del Cáncer, CSIC-University of Salamanca, Salamanca, Spain.
Xosé R BusteloCentro de Investigación del Cáncer, CSIC-University of Salamanca, Salamanca, Spain.
Pablo Lorenzano MennaNational Scientific and Technical Research Council (CONICET), Buenos Aires, Argentina.
Daniel E GomezLaboratory of Molecular Oncology, National University of Quilmes, Bernal, Argentina.
Centro de Investigación Biomédica en Red de Cáncer · ESNational University of Quilmes · ARCentro Científico Tecnológico - San Juan · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last years, the development of new drugs in oncology has evolved notably. In particular, drug development has shifted from empirical screening of active cytotoxic compounds to molecularly targeted drugs blocking specific biologic pathways that drive cancer progression and metastasis. Using a rational design approach, our group has developed 1A-116 as a promising Rac1 inhibitor, with antitumoral and antimetastatic effects in several types of cancer. Rac1 is over activated in a wide range of tumor types and and it is one of the most studied proteins of the Rho GTPase family. Its role in actin cytoskeleton reorganization has effects on endocytosis, vesicular trafficking, cell cycle progression and cellular migration. In this context, the regulatory activity of Rac1 affects several key processes in the course of the cancer including invasion and metastasis. The purpose of this preclinical study was to focus on the mode of action of 1A-116, conducting an interdisciplinary approach with

Indexed as

cancerdockingGTPasesinhibitorsmall-molecule

Identifiers

PMID32351958
PMCPMC7174510
OpenAlexW3017250292

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.