Evidence map›Paper›PMID 36875137›Full record

ArticleFrontiers in immunology2023

Precision immunointerception of EGFR-driven tumorigenesis for lung cancer prevention.

Jing Pan, Donghai Xiong, Qi Zhang, Katie Palen, Robert H Shoemaker, Bryon Johnson, Shizuko Sei, Yian Wang, Ming You

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Shared neoantigens for cancer immunotherapy.Molecular therapy. Oncology · 2025
    Review
  3. Article
  4. Article
  5. 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

9 authors at 3 institutions in 1 country.

Jing PanCenter for Cancer Prevention, Houston Methodist Cancer Center, Houston Methodist Research Institute, Houston, TX, United States.
Donghai XiongCenter for Cancer Prevention, Houston Methodist Cancer Center, Houston Methodist Research Institute, Houston, TX, United States.
Qi ZhangCenter for Cancer Prevention, Houston Methodist Cancer Center, Houston Methodist Research Institute, Houston, TX, United States.
Katie PalenDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, United States.
Robert H ShoemakerChemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD, United States.
Bryon JohnsonDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, United States.
Shizuko SeiChemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, Bethesda, MD, United States.
Yian WangCenter for Cancer Prevention, Houston Methodist Cancer Center, Houston Methodist Research Institute, Houston, TX, United States.
Ming YouCenter for Cancer Prevention, Houston Methodist Cancer Center, Houston Methodist Research Institute, Houston, TX, United States.
Medical College of Wisconsin · USHouston Methodist · USNational Cancer Institute · US

Funding

Transfer Application - R01 CA223804 - Chemoimmunoprevention of EGFR-Driven Non-Small Cell Lung CancerR01CA223804 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WANG, LI LILY, YOU, MING · 2018 to 2022
$3.3M
Chemoprevention of Lung Cancer with Mitochondria-Targeted HonokiolR01CA208648 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KALYANARAMAN, BALARAMAN, YOU, MING · 2017 to 2021
$3.1M
Chemoprevention of lung cancer by targeting lonidamine to mitochondriaR01CA232433 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KALYANARAMAN, BALARAMAN, KRESTY, LAURA A · 2019 to 2023
$2.0M
NCI NIH HHS R01 CA208648NCI NIH HHS R01 CA223804NCI NIH HHS R01 CA232433
6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) mutations occur in about 50% of lung adenocarcinomas in Asia and about 15% in the US. EGFR mutation-specific inhibitors have been developed and made significant contributions to controlling EGFR mutated non-small cell lung cancer. However, resistance frequently develops within 1 to 2 years due to acquired mutations. No effective approaches that target mutant EGFR have been developed to treat relapse following tyrosine kinase inhibitor (TKI) treatment. Vaccination against mutant EGFR is one area of active exploration. In this study, we identified immunogenic epitopes for the common EGFR mutations in humans and formulated a multi-peptide vaccine (E

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsCarcinogenesisCell Transformation, NeoplasticErbB ReceptorsHumansMiceMutationNeoplasm Recurrence, LocalProtein Kinase InhibitorsTumor MicroenvironmentEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsEGFR mutationimmunointerceptionMHC class IIpeptide vaccineprecision immunopreventionT cell

Identifiers

PMID36875137
PMCPMC9982083
OpenAlexW4321233916

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.