Evidence map›Paper›PMID 39521886›Full record

ArticleOncogene2025

Nuclear EGFR in breast cancer suppresses NK cell recruitment and cytotoxicity.

Angelica Escoto, Ryan Hecksel, Chance Parkinson, Sara Crane, Benjamin Atwell, Shyanne King, Daniela Ortiz Chavez, Alison Jannuzi, Barbara Sands, Benjamin G Bitler and 4 more

Abstract read
In one paragraph

Article in Oncogene, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. EGFR: New Insights on Its Activation and Mutation in Tumor and Tumor Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  8. 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

14 authors.

Angelica EscotoUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.ORCID 0000-0003-0214-2718
Ryan HeckselUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.ORCID 0000-0003-4189-6950
Chance ParkinsonUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Sara CraneUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Benjamin AtwellUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Shyanne KingUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.ORCID 0000-0001-9345-0622
Daniela Ortiz ChavezUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Alison JannuziUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Barbara SandsUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Benjamin G BitlerDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.ORCID 0000-0002-5809-5271
Todd A FehnigerDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Andrew L PaekUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA.
Megha PadiUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA. mpadi@arizona.edu.
Joyce SchroederUniversity of Arizona Department of Molecular and Cellular Biology, Tucson, AZ, 85721, USA. joyces@arizona.edu.ORCID 0000-0003-1277-5172

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Targeting the Bone Marrow Microenvironment In Acute Lymphocytic LeukemiaP50CA171963 · NCI · WASHINGTON UNIVERSITY · PI Daniel C Link · 2013 to 2026
$31.6M
MARC/Biomedical Research and Training Program at the University of ArizonaT34GM008718 · NIGMS · UNIVERSITY OF ARIZONA · PI MIRANDA, KATRINA M. · 1999 to 2021
$8.6M
GRADUATE TRAINING IN BIOCHEMISTRY AND MOLECULAR BIOLOGYT32GM008659 · NIGMS · UNIVERSITY OF ARIZONA · PI CAPALDI, ANDREW PAUL, WEINERT, TED A. · 1997 to 2019
$5.3M
University of Arizona's Initiative for Maximizing Student Development (IMSD)T32GM139779 · NIGMS · UNIVERSITY OF ARIZONA · PI FRANS E TAX · 2022 to 2026
$2.9M
Targeting Wnt signaling in therapy-resistant ovarian cancerR37CA261987 · NCI · UNIVERSITY OF COLORADO DENVER · PI Benjamin G Bitler · 2021 to 2026
$2.4M
Graduate Training in Biochemistry and Molecular BiologyT32GM136536 · NIGMS · UNIVERSITY OF ARIZONA · PI Andrew Paul Capaldi, FRANS E TAX · 2020 to 2026
$2.4M
Dynamics of the FOXO transcription factor networkR01GM130864 · NIGMS · UNIVERSITY OF ARIZONA · PI PAEK, ANDREW LUTHER · 2019 to 2023
$1.7M
Unraveling the regulatory circuits that drive Merkel cell carcinomaR01CA251729 · NCI · UNIVERSITY OF ARIZONA · PI PADI, MEGHA · 2021 to 2025
$1.7M
NCI NIH HHS P30 CA023074NCI NIH HHS P30 CA091842NCI NIH HHS P50 CA171963NCI NIH HHS R01 CA251729NCI NIH HHS R37 CA261987NIGMS NIH HHS R01 GM130864NIGMS NIH HHS T32 GM008659NIGMS NIH HHS T32 GM136536NIGMS NIH HHS T32 GM139779NIGMS NIH HHS T34 GM008718
6 · The paper itself

Abstract

Natural Killer (NK) cells can target and destroy cancer cells, yet tumor microenvironments typically suppress NK cell recruitment and cytotoxicity. The epidermal growth factor receptor (EGFR) is a potent oncogene that can activate survival, migration, and proliferation pathways, and clinical data suggests it may also play an immunomodulating role in cancers. Recent work has demonstrated a novel role for nuclear EGFR (nEGFR) in regulating transcriptional events unique from the kinase domain. Using a novel peptide therapeutic (cSNX1.3) that inhibits retrograde trafficking of EGFR and an EGFR nuclear localization mutant, we discovered that nEGFR suppresses NK cell recruitment and cytotoxicity. RNA-Seq analysis of breast cancer cells treated with cSNX1.3 or modified to lack a nuclear localization sequence (EGFR

Indexed as

Breast NeoplasmsCytotoxicity, ImmunologicErbB ReceptorsKiller Cells, NaturalAnimalsCell Line, TumorCell NucleusFemaleHumansMiceMice, TransgenicTumor MicroenvironmentEGFR protein, humanErbB Receptors

Identifiers

PMID39521886
PMCPMC11779631

What OpenQuestion holds

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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.