Evidence map›Paper›PMID 30320548›Full record

ArticleeLife2018

RalB directly triggers invasion downstream Ras by mobilizing the Wave complex.

Giulia Zago, Irina Veith, Manish Kumar Singh, Laetitia Fuhrmann, Simon De Beco, Amanda Remorino, Saori Takaoka, Marjorie Palmeri, Frédérique Berger, Nathalie Brandon and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

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  5. [RGL1 overexpression promotes metastasis of colorectal cancer by upregulating motile focal adhesion assemblyNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
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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

15 authors at 4 institutions in 1 country.

Giulia ZagoInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.ORCID http://orcid.org/0000-0001-8280-1589
Irina VeithInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Manish Kumar SinghInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Laetitia FuhrmannInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Simon De BecoInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Amanda RemorinoInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Saori TakaokaInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Marjorie PalmeriInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Frédérique BergerInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Nathalie BrandonInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Ahmed El MarjouInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Anne Vincent-SalomonInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Jacques CamonisInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Mathieu CoppeyInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.
Maria Carla ParriniInstitut Curie, Centre de Recherche, Paris Sciences et Lettres Research University, Paris, France.ORCID http://orcid.org/0000-0002-7082-9792
Inserm · FRInstitut Curie · FRPhysique des Cellules et Cancers · FRExpression Génétique Microbienne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The two Ral GTPases, RalA and RalB, have crucial roles downstream Ras oncoproteins in human cancers; in particular, RalB is involved in invasion and metastasis. However, therapies targeting Ral signalling are not available yet. By a novel optogenetic approach, we found that light-controlled activation of Ral at plasma-membrane promotes the recruitment of the Wave Regulatory Complex (WRC) via its effector exocyst, with consequent induction of protrusions and invasion. We show that active Ras signals to RalB via two RalGEFs (Guanine nucleotide Exchange Factors), RGL1 and RGL2, to foster invasiveness; RalB contribution appears to be more important than that of MAPK and PI3K pathways. Moreover, on the clinical side, we uncovered a potential role of RalB in human breast cancers by determining that RalB expression at protein level increases in a manner consistent with progression toward metastasis. This work highlights the Ras-RGL1/2-RalB-exocyst-WRC axis as appealing target for novel anticancer strategies.

Indexed as

Breast NeoplasmsCell LineCell MembraneCell Surface ExtensionsDisease ProgressionFemaleHumansLightNeoplasm InvasivenessOptogeneticsral GTP-Binding Proteinsras ProteinsSignal TransductionWiskott-Aldrich Syndrome Protein FamilyRalb protein, humanral GTP-Binding Proteinsras ProteinsWiskott-Aldrich Syndrome Protein Familybreast cancercell biologyExocysthumanInvasionoptogeneticsRalWave

Identifiers

PMID30320548
PMCPMC6226288
OpenAlexW2897468627

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.