Evidence map›Paper›PMID 28498728›Full record

ReviewSmall GTPases2019

A family affair: A Ral-exocyst-centered network links Ras, Rac, Rho signaling to control cell migration.

Giulia Zago, Marco Biondini, Jacques Camonis, Maria Carla Parrini

Open access · bronzeAbstract readReviewVideo-Audio Media
In one paragraph

Review in Small GTPases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
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  4. Cryo-EM structure revealed a novel F-actin binding motif in abioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Current issues in molecular biology · 2025
    Article
  7. Review
  8. The role ofFrontiers in microbiology · 2024
    Review
  9. Silencing Rac1 and Prex1 Inhibit Epithelial-Mesenchymal Transition in Human Gastric Cancer Cells Induced by Transforming Growth Factor-β1.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Article
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  15. Article
  16. Review
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  18. Review
  19. A Series of Tubes: TheJournal of developmental biology · 2020
    Review
  20. Review
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 1 institution in 1 country.

Giulia Zagoa Institut Curie, Centre de Recherche, Paris Sciences et Lettres Research University , Paris , France.
Marco Biondinia Institut Curie, Centre de Recherche, Paris Sciences et Lettres Research University , Paris , France.
Jacques Camonisa Institut Curie, Centre de Recherche, Paris Sciences et Lettres Research University , Paris , France.
Maria Carla Parrinia Institut Curie, Centre de Recherche, Paris Sciences et Lettres Research University , Paris , France.
Institut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell migration is central to many developmental, physiologic and pathological processes, including cancer progression. The Ral GTPases (RalA and RalB) which act down-stream the Ras oncogenes, are key players in the coordination between membrane trafficking and actin polymerization. A major direct effector of Ral, the exocyst complex, works in polarized exocytosis and is at the center of multiple protein-protein interactions that support cell migration by promoting protrusion formation, front-rear polarization, and extra-cellular matrix degradation. In this review we describe the recent advancements in deciphering the molecular mechanisms underlying this role of Ral via exocyst on cell migration. Among others, we will discuss the recently identified cross-talk between Ral and Rac1 pathways: exocyst binds to a negative regulator (the RacGAP SH3BP1) and to the major effector (the Wave Regulatory Complex, WRC) of Rac1, the master regulator of protrusions. Next challenge will be to better characterize the dynamics in space and in time of these molecular interplays, to better understand the pleiotropic functions of Ral in both normal and cancer cells.

Indexed as

Cell MovementSignal TransductionAnimalsGTPase-Activating ProteinsHumansNeoplasm ProteinsNeoplasmsrac1 GTP-Binding Proteinral GTP-Binding Proteinsras ProteinsGTPase-Activating ProteinsNeoplasm Proteinsrac1 GTP-Binding ProteinRAC1 protein, humanRALA protein, humanRalb protein, humanral GTP-Binding Proteinsras ProteinsSH3BP1 protein, humanexocystmigrationRacRalRasRhoWave

Identifiers

PMID28498728
PMCPMC6748358
OpenAlexW2613704359

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.