Evidence map›Paper›PMID 42668613›Full record

ArticleClinical and translational radiation oncology2026

Pan-cancer analysis of Notch pathway-linked gene expression identifies tumour-specific and sex-stratified prognostic associations.

Helen O'Hea, V Bourbonne, Laure Marignol

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Article in Clinical and translational radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Helen O'HeaTrinity St. James's Cancer Institute, Radiobiology and Molecular Oncology Research Group, Applied Radiation Therapy Trinity, Discipline of Radiation Therapy, Trinity College Dublin, Ireland.
V BourbonneTrinity St. James's Cancer Institute, Radiobiology and Molecular Oncology Research Group, Applied Radiation Therapy Trinity, Discipline of Radiation Therapy, Trinity College Dublin, Ireland.
Laure MarignolTrinity St. James's Cancer Institute, Radiobiology and Molecular Oncology Research Group, Applied Radiation Therapy Trinity, Discipline of Radiation Therapy, Trinity College Dublin, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Notch signalling pathway regulates cell fate, proliferation, and differentiation and consists of receptors (Notch1-4), ligands (JAG1-2, DLL1, DLL3-4), and downstream targets. Altered expression of Notch pathway-linked genes has been reported in multiple cancers, although their associations with survival may vary according to tumour type. Their relationship with biological sex and radiotherapy (RT) has been less extensively explored. Purpose: To explore associations between Notch pathway-linked gene expression and overall survival (OS) across multiple cancer types, and to examine whether these associations differ by biological sex or in an RT-treated lung cancer subgroup. Methodology: Gene expression and clinical data from patients across nine cancer types were analysed using publicly available datasets derived from The Cancer Genome Atlas (TCGA) and the Kaplan-Meier Plotter platform. Associations between the expression of 14 Notch pathway-linked genes and OS were evaluated using Kaplan-Meier survival analyses. Representative findings were further evaluated using multivariable Cox proportional hazards models incorporating clinical covariates and gene expression × sex interaction terms. Main findings: Across nine cancer types, 13 of the 14 Notch pathway-linked genes were significantly associated with OS in at least one tumour type. DLL3 and JAG1 demonstrated recurrent associations across multiple cancers, with higher DLL3 expression more frequently associated with poorer OS. Sex-stratified analyses identified additional prognostic associations; however, multivariable interaction analyses did not consistently support biological sex as an effect modifier. In the RT-treated lung adenocarcinoma subgroup, higher Conclusion: This exploratory pan-cancer analysis identified associations between the expression of several Notch pathway-linked genes and OS, including recurrent associations involving

Indexed as

Biological sexCancerNotchOutcomeSurvival

Identifiers

PMID42668613
PMCPMC13524761

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