Evidence map›Paper›PMID 38182563›Full record

ArticleCell death & disease2024

GRB2 is a BECN1 interacting protein that regulates autophagy.

Jetsy Montero-Vergara, Kira Plachetta, Lisa Kinch, Stephan Bernhardt, Kriti Kashyap, Beth Levine, Lipi Thukral, Martina Vetter, Christoph Thomssen, Stefan Wiemann and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. The Biological Role and Clinical Significance of BECLIN-1 in Cancer.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
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

13 authors at 5 institutions in 3 countries.

Jetsy Montero-VergaraInstitute of Cell Biology (Cancer Research), University Hospital Essen, Virchowstrasse 173, D-45122, Essen, Germany.
Kira PlachettaInstitute of Cell Biology (Cancer Research), University Hospital Essen, Virchowstrasse 173, D-45122, Essen, Germany.
Lisa KinchUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390, USA.
Stephan BernhardtDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, D-69120, Heidelberg, Germany.
Kriti KashyapCSIR-Institute of Genomics and Integrative Biology, Mathura Road, New Delhi, Delhi, 110025, India.
Beth LevineUniversity of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390, USA.
Lipi ThukralCSIR-Institute of Genomics and Integrative Biology, Mathura Road, New Delhi, Delhi, 110025, India.
Martina VetterDepartment of Gynaecology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, D-06120, Halle (Saale), Germany.ORCID 0000-0002-6642-9585
Christoph ThomssenDepartment of Gynaecology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, D-06120, Halle (Saale), Germany.
Stefan WiemannDivision of Molecular Genome Analysis, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, D-69120, Heidelberg, Germany.ORCID 0000-0003-4683-3174
Samuel Peña-LlopisTranslational Genomics. Department of Ophthalmology, University Hospital Essen, Essen, Germany.
Verena JendrossekInstitute of Cell Biology (Cancer Research), University Hospital Essen, Virchowstrasse 173, D-45122, Essen, Germany.ORCID 0000-0003-1058-2107
Silvia Vega-Rubin-de-CelisInstitute of Cell Biology (Cancer Research), University Hospital Essen, Virchowstrasse 173, D-45122, Essen, Germany. Silvia.VegaRubindeCelis@UK-Essen.de.ORCID 0000-0002-4196-8996
Essen University Hospital · DEGerman Cancer Research Center · DEInstitute of Genomics and Integrative Biology · INMartin Luther University Halle-Wittenberg · DEThe University of Texas Southwestern Medical Center · US

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) VE1153/1-1EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 798637
6 · The paper itself

Abstract

GRB2 is an adaptor protein of HER2 (and several other tyrosine kinases), which we identified as a novel BECN1 (Beclin 1) interacting partner. GRB2 co-immunoprecipitated with BECN1 in several breast cancer cell lines and regulates autophagy through a mechanism involving the modulation of the class III PI3Kinase VPS34 activity. In ovo studies in a CAM (Chicken Chorioallantoic Membrane) model indicated that GRB2 knockdown, as well as overexpression of GRB2 loss-of-function mutants (Y52A and S86A-R88A) compromised tumor growth. These differences in tumor growth correlated with differential autophagy activity, indicating that autophagy effects might be related to the effects on tumorigenesis. Our data highlight a novel function of GRB2 as a BECN1 binding protein and a regulator of autophagy.

Indexed as

AutophagyBeclin-1GRB2 Adaptor ProteinAdaptor Proteins, Signal TransducingAnimalsCarcinogenesisCell Transformation, NeoplasticHumansAdaptor Proteins, Signal TransducingBeclin-1BECN1 protein, humanGRB2 Adaptor ProteinGRB2 protein, human

Identifiers

PMID38182563
PMCPMC10770341
OpenAlexW4390617744

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.