Evidence map›Paper›PMID 42249069›Full record

ArticleCommunications medicine2026

Multidimensional proteomics and explainable AI feature selection identify cross-platform lung cancer molecular signature in blood plasma.

Nikola Gushterov, Luke Hankey, Iliyana Kaneva, Mrunmayee Dupalliwar, Junetha Syed, Emma Mi, Ella Mi, Daniel Andrzej Szulc, Luna Jia Zhan, Devalben Patel and 5 more

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Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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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

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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

1 citing paper in PubMed.

  1. 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

15 authors.

Nikola Gushterov *Oxford Cancer Analytics Ltd, Oxford, UK.
Luke Hankey *Oxford Cancer Analytics Ltd, Oxford, UK.ORCID http://orcid.org/0000-0001-5192-9571
Iliyana Kaneva *Oxford Cancer Analytics Ltd, Oxford, UK.ORCID http://orcid.org/0000-0002-2253-9811
Mrunmayee DupalliwarOxford Cancer Analytics Ltd, Oxford, UK.
Junetha SyedOxford Cancer Analytics Ltd, Oxford, UK.
Emma MiOxford Cancer Analytics Ltd, Oxford, UK.
Ella MiOxford Cancer Analytics Ltd, Oxford, UK.
Daniel Andrzej SzulcOxford Cancer Analytics Ltd, Oxford, UK.
Luna Jia ZhanPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Devalben PatelPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Roman FischerTarget Discovery Institute, Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-9715-5951
Benedikt M KesslerTarget Discovery Institute, Centre for Medicines Discovery, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-8160-2446
Geoffrey LiuPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Andreas HalnerOxford Cancer Analytics Ltd, Oxford, UK.
Peter Jianrui LiuOxford Cancer Analytics Ltd, Oxford, UK. peterjr.liu@mail.utoronto.ca.ORCID http://orcid.org/0000-0003-3608-750X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is the leading cause of cancer mortality worldwide despite the availability of low-dose computed tomography (LDCT) for screening in high-risk populations.

methodsTo develop an approach and identify blood-based protein signatures for lung cancer that can be deployed across platforms, we combined data-independent acquisition mass-spectrometry (DIA-MS) and proximity extension assay (PEA) with explainable artificial intelligence (XAI)-led machine learning (ML) for plasma-based biomarker discovery. Using a cohort of 490 lung cancer patients and 124 matched controls, ML models were trained to predict lung cancer and XAI was used to characterise networks of model-consistent features. We then introduced a DNA-aptamer based proteomic approach to assess cross-platform concordance and define a cross-platform signature. This signature was subsequently evaluated using an external cohort.

resultsHere we show that ML models achieve an AUROC of 0.91 [95% CI: 0.88-0.93] and 0.97 [95% CI: 0.92-0.98] in DIA-MS and PEA, respectively, using a 80/20% train/holdout split. XAI further characterises networks of model-consistent features related to chemotaxis, cell adhesion, wound healing and immune response. Introduction of the DNA-aptamer proteomic approach identifies a cross-platform signature, with performances of 0.88 [95% CI: 0.80-0.90] and 0.88 [95% CI: 0.81-0.95] in DIA-MS and PEA, respectively. Assessment of this signature in an external cohort separates lung cancer from control cases.

conclusionsThis study develops an approach combining multi-dimensional proteomics with XAI-ML and demonstrates the characterisation of cross-platform biomarker signatures for lung cancer.

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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.