Evidence map›Paper›PMID 28661476›Full record

ArticleCell death & disease2017

Ubiquitin-dependent regulation of Cdc42 by XIAP.

Arun Murali, Jaeyoung Shin, Hajime Yurugi, Aswini Krishnan, Masato Akutsu, Alejandro Carpy, Boris Macek, Krishnaraj Rajalingam

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

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  8. Inhibition ofInternational journal of molecular sciences · 2023
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  17. Molecular subversion of Cdc42 signalling in cancer.Biochemical Society transactions · 2021
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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

8 authors at 3 institutions in 1 country.

Arun MuraliMolecular Signaling Unit-FZI, Institute of immunology, University Medical Center Mainz, JGU-Mainz, Germany.
Jaeyoung ShinMolecular Signaling Unit-FZI, Institute of immunology, University Medical Center Mainz, JGU-Mainz, Germany.
Hajime YurugiMolecular Signaling Unit-FZI, Institute of immunology, University Medical Center Mainz, JGU-Mainz, Germany.
Aswini KrishnanMolecular Signaling Unit-FZI, Institute of immunology, University Medical Center Mainz, JGU-Mainz, Germany.
Masato AkutsuBMLS, Goethe University, Frankfurt, Germany.
Alejandro CarpyProteome Center Tuebingen, Interfaculty Institute for Cell Biology, University of Tuebingen, Tuebingen, Germany.
Boris MacekProteome Center Tuebingen, Interfaculty Institute for Cell Biology, University of Tuebingen, Tuebingen, Germany.
Krishnaraj RajalingamMolecular Signaling Unit-FZI, Institute of immunology, University Medical Center Mainz, JGU-Mainz, Germany.
Johannes Gutenberg University Mainz · DEUniversity of Tübingen · DEGoethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rho GTPases control fundamental cellular processes and Cdc42 is a well-studied member of the family that controls filopodia formation and cell migration. Although the regulation of Cdc42 activity by nucleotide binding is well documented, the mechanisms driving its proteostasis are not clear. Here, we demonstrate that the highly conserved, RING domain containing E3 ubiquitin ligase XIAP controls the protein stability of Cdc42. XIAP binds to Cdc42 and directly conjugates poly ubiquitin chains to the Lysine 166 of Cdc42 targeting it for proteasomal degradation. Depletion of XIAP led to an increased protein stability and activity of Cdc42 in normal and tumor cells. Consistently, loss of XIAP enhances filopodia formation in a Cdc42-dependent manner and this phenomenon phenocopies EGF stimulation. Further, XIAP depletion promotes lung colonization of tumor cells in mice in a Cdc42-dependent manner. These observations shed molecular insights into ubiquitin-dependent regulation of Cdc42 and that of actin cytoskeleton.

Indexed as

Actin CytoskeletonAnimalsApoptosiscdc42 GTP-Binding ProteinCell MovementHeLa CellsHumansMiceNeoplasmsProtein StabilityPseudopodiaSignal TransductionUbiquitinUbiquitinationUbiquitin-Protein LigasesXenograft Model Antitumor Assayscdc42 GTP-Binding ProteinUbiquitinUbiquitin-Protein LigasesXIAP protein, humanX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID28661476
PMCPMC5520948
OpenAlexW2724425777

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.