Evidence map›Paper›PMID 33373873›Full record

ReviewNeoplasia (New York, N.Y.)2021

Tumor necrosis factor in lung cancer: Complex roles in biology and resistance to treatment.

Ke Gong, Gao Guo, Nicole Beckley, Yue Zhang, Xiaoyao Yang, Mishu Sharma, Amyn A Habib

Open access · goldAbstract readReview
In one paragraph

Review in Neoplasia (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 2 syntheses or guidelines pooled it, 83 citations in OpenAlex.

  1. Pooled it
  2. Systemic treatment of immune checkpoint inhibitor-induced psoriasis: Inference-based guidance.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Pooled it
  3. Article
  4. Article
  5. Article
  6. Endogenous targeting lipid nanoparticles for systemic mRNA delivery to lung cancer tumors.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Ke GongDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: Ke.Gong@UTSouthwestern.edu.
Gao GuoDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nicole BeckleyDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Yue ZhangDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Xiaoyao YangDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Mishu SharmaDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Amyn A HabibDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA; VA North Texas Health Care System, Dallas, TX, USA. Electronic address: Amyn.Habib@UTSouthwestern.edu.
The University of Texas Southwestern Medical Center · US

Funding

The role of Nrf2 in mediating resistance to EGFR inhibition in glioblastomaR01CA244212 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HABIB, AMYN · 2020 to 2024
$1.9M
BLRD VA I01 BX002559NCI NIH HHS R01 CA244212
6 · The paper itself

Abstract

Tumor necrosis factor (TNF) and its receptors are widely expressed in non-small cell lung cancer (NSCLC). TNF has an established role in inflammation and also plays a key role in inflammation-induced cancer. TNF can induce cell death in cancer cells and has been used as a treatment in certain types of cancer. However, TNF is likely to play an oncogenic role in multiple types of cancer, including NSCLC. TNF is a key activator of the transcription factor NF-κB. NF-κB, in turn, is a key effector of TNF in inflammation-induced cancer. Data from The Cancer Genome Atlas database suggest that TNF could be a biomarker in NSCLC and indicate a complex role for TNF and its receptors in NSCLC. Recent studies have reported that TNF is rapidly upregulated in NSCLC in response to targeted treatment with epidermal growth factor receptor (EGFR) inhibition, and this upregulation leads to NF-κB activation. The TNF upregulation and consequent NF-κB activation play a key role in mediating both primary and secondary resistance to EGFR inhibition in NSCLC, and a combined inhibition of EGFR and TNF can overcome therapeutic resistance in experimental models. TNF may mediate the toxic side effects of immunotherapy and may also modulate resistance to immune checkpoint inhibitors. Drugs inhibiting TNF are widely used for the treatment of various inflammatory and rheumatologic diseases and could be quite useful in combination with targeted therapy of NSCLC and other cancers.

Indexed as

Disease SusceptibilityAnimalsBiomarkersBiomarkers, TumorDisease ManagementDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGenomicsHumansLung NeoplasmsMolecular Targeted TherapyNF-kappa BPrognosisTreatment OutcomeTumor Necrosis FactorsBiomarkersBiomarkers, TumorNF-kappa BTumor Necrosis FactorsEGFR inhibitionImmunotherapyNSCLCTCGATherapeutic resistanceTNF

Identifiers

PMID33373873
PMCPMC7773536
OpenAlexW3113963435

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.