Evidence map›Paper›PMID 27152953›Full record

ArticleCell cycle (Georgetown, Tex.)2016

Proteomic analysis of Rac1 signaling regulation by guanine nucleotide exchange factors.

Hadir Marei, Alejandro Carpy, Boris Macek, Angeliki Malliri

Open access · hybridAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. PUFA-DerivedACS chemical biology · 2022
    Article
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  5. Article
  6. Review
  7. P-Rex1 Mediates Glucose-Stimulated Rac1 Activation and Insulin Secretion in Pancreatic β-Cells.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2020
    Article
  8. Review
  9. Review
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  11. Article
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  15. 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 2 institutions in 2 countries.

Hadir Mareia Cell Signaling Group, Cancer Research UK Manchester Institute, The University of Manchester , Manchester , UK.
Alejandro Carpyb Proteome Center Tuebingen, Interfaculty Institute for Cell Biology, University of Tuebingen , Tuebingen , Germany.
Boris Macekb Proteome Center Tuebingen, Interfaculty Institute for Cell Biology, University of Tuebingen , Tuebingen , Germany.
Angeliki Malliria Cell Signaling Group, Cancer Research UK Manchester Institute, The University of Manchester , Manchester , UK.
University of Manchester · GBUniversity of Tübingen · DE

Funding

Cancer Research UK 20410
6 · The paper itself

Abstract

The small GTPase Rac1 is implicated in various cellular processes that are essential for normal cell function. Deregulation of Rac1 signaling has also been linked to a number of diseases, including cancer. The diversity of Rac1 functioning in cells is mainly attributed to its ability to bind to a multitude of downstream effectors following activation by Guanine nucleotide Exchange Factors (GEFs). Despite the identification of a large number of Rac1 binding partners, factors influencing downstream specificity are poorly defined, thus hindering the detailed understanding of both Rac1's normal and pathological functions. In a recent study, we demonstrated a role for 2 Rac-specific GEFs, Tiam1 and P-Rex1, in mediating Rac1 anti- versus pro-migratory effects, respectively. Importantly, via conducting a quantitative proteomic screen, we identified distinct changes in the Rac1 interactome following activation by either GEF, indicating that these opposing effects are mediated through GEF modulation of the Rac1 interactome. Here, we present the full list of identified Rac1 interactors together with functional annotation of the differentially regulated Rac1 binding partners. In light of this data, we also provide additional insights into known and novel signaling cascades that might account for the GEF-mediated Rac1-driven cellular effects.

Indexed as

Signal TransductionAnimalsCell CommunicationCell Line, TumorCell MovementGuanine Nucleotide Exchange FactorsHumansIsotope LabelingMiceNIH 3T3 CellsProtein BindingProtein Interaction MappingProteomicsrac1 GTP-Binding Proteinras GTPase-Activating ProteinsGuanine Nucleotide Exchange FactorsIQ motif containing GTPase activating protein 1rac1 GTP-Binding Proteinras GTPase-Activating ProteinsGuanine nucleotide Exchange Factors (GEFs)Ingenuity Integrated Pathway Analysis (IPA)IQGAP1P-Rex1Rac1Small GTPasesStable Isotope Labeling by Amino acids in Cell culture (SILAC)Tandem Affinity Purification (TAP)Tiam1TMOD3

Identifiers

PMID27152953
PMCPMC4968972
OpenAlexW2345781389

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.