Evidence map›Paper›PMID 41332426›Full record

ArticleCancer biology & therapy2025

Toll-like receptor 4 inhibition sensitizes non-small cell lung cancer to radiotherapy.

Ryma Haroun, Cleopatra Rutihinda, Aissatou Hadja Diallo, Juan Pablo Ordonez, Sahar Nassri, Aliya Shams, Maria Fernanda Meza Pacheco, Nour Elhouda Saidi, Lea Bouchard, Guy-Anne Turgeon and 3 more

Abstract read
In one paragraph

Article in Cancer biology & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

Ryma HarounDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.ORCID 0009-0002-7475-6268
Cleopatra RutihindaDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Aissatou Hadja DialloDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Juan Pablo OrdonezDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Sahar NassriDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Aliya ShamsDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Maria Fernanda Meza PachecoDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Nour Elhouda SaidiDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Lea BouchardDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Guy-Anne TurgeonDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Denis GrisDepartment of Pharmacology and Physiology, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Lee-Hwa TaiDepartment of Immunology and Cell Biology, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.
Ayman J OweidaDepartment of Medical Imaging and Radiation Sciences, Faculty of Medicine and Health Sciences, Université of Sherbrooke, Sherbrooke, Quebec, Canada.ORCID 0000-0003-1256-4893

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small-cell lung cancer (NSCLC) is the leading cause of cancer-related mortality worldwide. Although radiotherapy (RT) is used to treat over half of NSCLC patients, about 30% have inherent or acquired radioresistance leading to treatment failure. There's a clinically unmet need to investigate mechanisms of radioresistance that can be targeted in combination with RT. Among these, HMGB1 has been shown to play a key role in tumor progression. Our research investigates TLR4, a receptor for HMGB1, highly expressed in NSCLC tissues, as a mediator of radioresistance.

methodsThe TLR4 inhibitor, TAK242, was tested in NSCLC cell lines (murine: LLCI, KLN205; human: H1975, SW900). Cells were irradiated at 2 and 10 Gy.

resultsTAK242 significantly decreased NSCLC cell proliferation and migration. Radiation at 2 and 10 Gy increased TLR4 gene expression

conclusionThese findings show that TLR4 inhibition enhances RT sensitivity in NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsRadiation-Sensitizing AgentsRadiation ToleranceToll-Like Receptor 4AnimalsCell Line, TumorCell ProliferationHMGB1 ProteinHumansMiceSulfonamidesXenograft Model Antitumor Assaysethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylateHMGB1 ProteinRadiation-Sensitizing AgentsSulfonamidesTLR4 protein, humanToll-Like Receptor 4HMGB1immunotherapynon-small cell lung cancerradioresistanceRadiotherapytoll-like receptor 4

Identifiers

PMID41332426
PMCPMC12688242

What Socratic 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 Socratic graph.