Evidence map›Paper›PMID 37474760›Full record

ArticleCommunications biology2023

EHD1-dependent traffic of IGF-1 receptor to the cell surface is essential for Ewing sarcoma tumorigenesis and metastasis.

Sukanya Chakraborty, Aaqib M Bhat, Insha Mushtaq, Haitao Luan, Achyuth Kalluchi, Sameer Mirza, Matthew D Storck, Nagendra Chaturvedi, Jose Antonio Lopez-Guerrero, Antonio Llombart-Bosch and 9 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. mCancer communications (London, England) · 2025
    Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 4 countries.

Sukanya ChakrabortyEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Aaqib M BhatEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Insha MushtaqEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Haitao LuanEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Achyuth KalluchiDepartment of Genetics, Cell Biology & Anatomy, College of Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Sameer MirzaDepartment of Genetics, Cell Biology & Anatomy, College of Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Matthew D StorckEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Nagendra ChaturvediDepartment of Pediatrics, University of Nebraska Medical Center, Omaha, NE, 68198, USA.ORCID 0000-0001-7037-898X
Jose Antonio Lopez-GuerreroLaboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.ORCID 0000-0002-7369-8388
Antonio Llombart-BoschDepartment of Pathology, University of Valencia, Avd. Blasco Ibáñez 15, 46010, Valencia, Spain.
Isidro MachadoDepartment of Pathology, University of Valencia, Avd. Blasco Ibáñez 15, 46010, Valencia, Spain.
Katia ScotlandiLaboratory of Experimental Oncology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.ORCID 0000-0001-6114-9499
Jane L MezaDepartment of Biostatistics, College of Public Health, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Gargi GhosalDepartment of Genetics, Cell Biology & Anatomy, College of Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Donald W CoulterDepartment of Pediatrics, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
M Jordan RowleyDepartment of Genetics, Cell Biology & Anatomy, College of Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA.ORCID 0000-0002-5135-9596
Vimla BandDepartment of Genetics, Cell Biology & Anatomy, College of Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Bhopal C MohapatraDepartment of Genetics, Cell Biology & Anatomy, College of Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA. bmohapat@unmc.edu.ORCID 0000-0003-3434-4306
Hamid BandEppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, 68198, USA. hband@unmc.edu.ORCID 0000-0002-4996-9002
University of Nebraska Medical Center · USNebraska Medical Center · USUniversitat de València · ESFundación Instituto Valenciano de Oncología · ESIstituto Ortopedico Rizzoli · ITUnited Arab Emirates University · AE

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Fine-Scale Genome Folding Relative to Transcription and LocationR35GM147467 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Michael Jordan Rowley · 2022 to 2026
$2.0M
Mechanisms underlying USP1-mediated bypass of EWS-FLI1 oncogene-induced replication stress in Ewing sarcomaR01CA263504 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GARGI GHOSAL · 2022 to 2026
$1.7M
Regulation of SPRTN protease and SPRTN-mediated DNA-Protein Crosslink RepairR01GM141232 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GHOSAL, GARGI · 2022 to 2025
$1.3M
Ecdysoneless, A Novel Regulator of Androgen ReceptorR21CA241055 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, VIMLA · 2019 to 2020
$379k
Co-Oncogenic Role of ECD in HER2-Driven Breast CancerR03CA253193 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAND, VIMLA · 2021 to 2022
$153k
NCI NIH HHS P30 CA036727NCI NIH HHS R01 CA263504NCI NIH HHS R03 CA253193NCI NIH HHS R21 CA241055NIGMS NIH HHS R01 GM141232NIGMS NIH HHS R35 GM147467
6 · The paper itself

Abstract

Overexpression of the EPS15 Homology Domain containing 1 (EHD1) protein has been linked to tumorigenesis but whether its core function as a regulator of intracellular traffic of cell surface receptors plays a role in oncogenesis remains unknown. We establish that EHD1 is overexpressed in Ewing sarcoma (EWS), with high EHD1 mRNA expression specifying shorter patient survival. ShRNA-knockdown and CRISPR-knockout with mouse Ehd1 rescue established a requirement of EHD1 for tumorigenesis and metastasis. RTK antibody arrays identified IGF-1R as a target of EHD1 regulation in EWS. Mechanistically, we demonstrate a requirement of EHD1 for endocytic recycling and Golgi to plasma membrane traffic of IGF-1R to maintain its surface expression and downstream signaling. Conversely, EHD1 overexpression-dependent exaggerated oncogenic traits require IGF-1R expression and kinase activity. Our findings define the RTK traffic regulation as a proximal mechanism of EHD1 overexpression-dependent oncogenesis that impinges on IGF-1R in EWS, supporting the potential of IGF-1R and EHD1 co-targeting.

Indexed as

Sarcoma, EwingAnimalsCarcinogenesisCell MembraneCell Transformation, NeoplasticMiceReceptor, IGF Type 1Signal TransductionReceptor, IGF Type 1

Identifiers

PMID37474760
PMCPMC10359273
OpenAlexW4384925078

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.