Evidence map›Paper›PMID 34622577›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

Cellular Origins of EGFR-Driven Lung Cancer Cells Determine Sensitivity to Therapy.

Fan Chen, Jinpeng Liu, Robert M Flight, Kassandra J Naughton, Alexsandr Lukyanchuk, Abigail R Edgin, Xiulong Song, Haikuo Zhang, Kwok-Kin Wong, Hunter N B Moseley and 2 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. An Agrin-YAP/TAZ Rigidity Sensing Module Drives EGFR-Addicted Lung Tumorigenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  7. Review
  8. Article
  9. Using 3-Dimensional Cultures to Propagate Genetically Modified Lung Organoids.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  10. Article
  11. Article
  12. Using Artificial Intelligence to Identify Tumor Microenvironment Heterogeneity in Non-Small Cell Lung Cancers.Laboratory investigation; a journal of technical methods and pathology · 2023
    Article
  13. The application of patient-derived organoid in the research of lung cancer.Cellular oncology (Dordrecht, Netherlands) · 2023
    Review
  14. Review
  15. Article
  16. Review
  17. [Lung Cancer Stem-like Cells and Drug Resistance].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2022
    Review
  18. Article
  19. Cellular Origins of EGFR-Driven Lung Cancer Cells Determine Sensitivity to Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    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

12 authors at 3 institutions in 1 country.

Fan ChenDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Jinpeng LiuDepartment of Internal Medicine, University of Kentucky, Lexington, KY, 40536, USA.
Robert M FlightDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY, 40536, USA.
Kassandra J NaughtonDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Alexsandr LukyanchukDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Abigail R EdginDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Xiulong SongDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Haikuo ZhangDNAtrix, 10355 Science Center Drive, Suite 110, San Diego, CA, 92121, USA.
Kwok-Kin WongLaura and Isaac Perlmutter Cancer Center, NYU Langone Medical Center, New York University, New York, NY, 10016, USA.
Hunter N B MoseleyDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.
Chi WangDepartment of Internal Medicine, University of Kentucky, Lexington, KY, 40536, USA.
Christine F BrainsonDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA.ORCID 0000-0002-0854-5043
University of Kentucky · USDNAtrix (United States) · USNYU Langone Health · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
University of Kentucky Center for Cancer MetabolismP20GM121327 · NIGMS · UNIVERSITY OF KENTUCKY · PI Eunus Ali · 2017 to 2026
$25.0M
Targeting Epigenetic Heterogeneity to Improve Lung Cancer Immunotherapy ResponseR01CA237643 · NCI · UNIVERSITY OF KENTUCKY · PI BRAINSON, CHRISTINE FILLMORE · 2019 to 2023
$1.9M
Defining epigenetic vulnerabilities of subtype-specific lung cancersK22CA201036 · NCI · UNIVERSITY OF KENTUCKY · PI BRAINSON, CHRISTINE FILLMORE · 2016 to 2018
$482k
American Association for Cancer Research Innovation and Discovery Grant NIGMS P20 GM121327-03American Association for Cancer Research Innovation and Discovery Grant (C.F.B.) NIGMS P20 GM121327-03American Cancer Society Institutional Research Grant IRG-85-001-25American Cancer Society Institutional Research Grant NCI R01 CA237643American Cancer Society Research Scholar Grants 133123-RSG-19-081-01-TBGKentucky Lung Cancer Research Program NCI K22 CA201036NCI NIH HHS K22 CA201036NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA237643NIGMS NIH HHS P20 GM121327Oncogenomics Shared Resource Facility, Biospecimen Procurement and Translational Pathology Shared Resource Facility, Biostatistics and Bioinformatics Shared Resource Facility and Flow Cytometry and Immune Monitoring Shared Resource Facility of the University of Kentucky Markey Cancer Center P30CA177558
6 · The paper itself

Abstract

Targeting the epidermal growth factor receptor (EGFR) with tyrosine kinase inhibitors (TKIs) is one of the major precision medicine treatment options for lung adenocarcinoma. Due to common development of drug resistance to first- and second-generation TKIs, third-generation inhibitors, including osimertinib and rociletinib, have been developed. A model of EGFR-driven lung cancer and a method to develop tumors of distinct epigenetic states through 3D organotypic cultures are described here. It is discovered that activation of the EGFR T790M/L858R mutation in lung epithelial cells can drive lung cancers with alveolar or bronchiolar features, which can originate from alveolar type 2 (AT2) cells or bronchioalveolar stem cells, but not basal cells or club cells of the trachea. It is also demonstrated that these clones are able to retain their epigenetic differences through passaging orthotopically in mice and crucially that they have distinct drug vulnerabilities. This work serves as a blueprint for exploring how epigenetics can be used to stratify patients for precision medicine decisions.

Indexed as

AcrylamidesAniline CompoundsAnimalsAntineoplastic AgentsCell Line, TumorDisease Models, AnimalErbB ReceptorsFemaleHumansIndolesLung NeoplasmsMaleMiceMice, NudePrecision MedicineProtein Kinase InhibitorsAcrylamidesAniline CompoundsAntineoplastic AgentsErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidinesrociletinibalveolarbronchiolarEGFRlung cancerorganoids

Identifiers

PMID34622577
PMCPMC8596110
OpenAlexW3204341115

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.