Evidence map›Paper›PMID 29172947›Full record

ReviewSmall GTPases2020

Crosstalk between WIP and Rho family GTPases.

Inés M Antón, Carla Gómez-Oro, Sergio Rivas, Francisco Wandosell

Open access · bronzeAbstract readReview
In one paragraph

Review in Small GTPases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. The Rho GTPase signaling pathway modulatesFrontiers in immunology · 2026
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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 1 country.

Inés M AntónDepartamento de biología molecular y celular, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Carla Gómez-OroDepartamento de biología molecular y celular, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Sergio RivasDepartamento de biología molecular y celular, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Francisco WandosellCentro de Biología Molecular Severo Ochoa (CSIC-UAM), Madrid, Spain.
Centro Nacional de Biotecnología · ESBiomedical Research Networking Center on Neurodegenerative Diseases · ESCentro de Biología Molecular Severo Ochoa · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Through actin-binding proteins such as the neural Wiskott-Aldrich syndrome protein (N-WASP) and WASP-interacting protein (WIP), the Rho family GTPases RhoA, Rac1 and Cdc42 are major modulators of the cytoskeleton. (N-)WASP and WIP control Rho GTPase activity in various cell types, either by direct WIP/(N-)WASP/Cdc42 or potential WIP/RhoA binding, or through secondary links that regulate GTPase distribution and/or transcription levels. WIP helps to regulate filopodium generation and participates in the Rac1-mediated ruffle formation that determines cell motility. In neurons, lack of WIP increases dendritic spine size and filamentous actin content in a RhoA-dependent manner. In contrast, WIP deficiency in an adenocarcinoma cell line significantly reduces RhoA levels. These data support a role for WIP in the GTPase-mediated regulation of numerous actin-related cell functions; we discuss the possibility that this WIP effect is linked to cell proliferative status.

Indexed as

Humansrho GTP-Binding ProteinsWiskott-Aldrich Syndrome Proteinrho GTP-Binding ProteinsWiskott-Aldrich Syndrome Proteindifferentiationfilamentous actin/invasivenessproliferationRhoA

Identifiers

PMID29172947
PMCPMC7549614
OpenAlexW2768843258

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.