ArticleOpen life sciences2026
Irofulven and RSL3 synergistically target ferroptosis-related gene PTGR1 to treat head and neck squamous cell carcinoma.
Article in Open life sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Head and neck squamous cell carcinoma (HNSCC) is an aggressive form of cancer characterized by significant fatality rates and unfavorable clinical outcomes. Ferroptosis serves as a crucial mechanism in controlling oncogenesis and tumor growth. However, the strategy targeting ferroptosis-related gene to predict and treat HNSCC is still not clear. The study was designed to assess the potential of ferroptosis as a biomarker and therapeutic target in HNSCC. A prognostic model based on ferroptosis-related genes was constructed using least absolute shrinkage and selection operator (LASSO). Multi-omic analysis revealed that the model was closely related to DNA methylation, DNA mutation and immune infiltration. HNSCC classification and the risk score in each classification were identified by analyzing single-cell RNA-sequencing (scRNA-seq) data. The results demonstrated that the risk score in malignant tumor classification is the highest, which is relative to the progression of HNSCC. Furthermore, through CellMiner database, we found the small molecular drug irofulven could target the risk score-related gene prostaglandin reductase 1 (PTGR1), which could inhibit the ferroptosis levels in HNSCC. Importantly, irofulven and ferroptosis inducer RSL3 exerted significant synergistic effects on HNSCC
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.