Evidence map›Paper›PMID 41752130›Full record

ArticleInternational journal of molecular sciences2026

A Circulating Signature of Tumour Hybrid Cells and Immune Checkpoints Predicts Metastatic Progression in Lung Cancer.

Gonzalo Sáenz de Santa María-Diez, Sandra Liana Pardo-Prieto, Roberto Lozano-Rodríguez, Urko Aguirre-Larracoechea, María Elena Corpa-Rodríguez, Julia Del Prado-Montero, Verónica Terrón-Arcos, Karla Montalbán-Hernández, Daniel Arvelo-Rosario, Jesús Fernández-Felipe and 5 more

Abstract read
In one paragraph

Article in International journal of molecular 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Gonzalo Sáenz de Santa María-DiezThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Sandra Liana Pardo-PrietoThoracic Surgery Service, La Paz University Hospital, 28046 Madrid, Spain.
Roberto Lozano-RodríguezThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0003-0093-9707
Urko Aguirre-LarracoecheaResearch Unit, Osakidetza Basque Health Service, Barrualde-Galdakao Integrated Health Organisation, Galdakao-Usansolo Hospital, 48960 Galdakao, Spain.
María Elena Corpa-RodríguezThoracic Surgery Service, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0009-0005-6878-3640
Julia Del Prado-MonteroThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Verónica Terrón-ArcosThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Karla Montalbán-HernándezThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0002-1612-103X
Daniel Arvelo-RosarioThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Jesús Fernández-FelipeThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Laura CórdobaThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Gloria C Bonel-PérezThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0001-6546-3039
Carlos Del FresnoThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0003-1771-7254
Laura Hurtado-NavarroThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Eduardo López-CollazoThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer remains the leading cause of cancer-related mortality worldwide and is frequently diagnosed at advanced stages, when metastatic dissemination is already present. Tumour hybrid cells (THCs) are rare circulating cells formed through fusion between cancer stem cells with leukocytes, predominantly monocytes. These cells combine traits from both lineages, conferring enhanced migratory, invasive and immune-evasive capacities that could promote metastasis. In parallel, soluble immune checkpoints (sICs) have emerged as minimally invasive biomarkers and indicators of systemic immune dysregulation and tumour-driven immune escape. In this study, 31 patients with lung cancer were prospectively enrolled at La Paz University Hospital (Madrid, Spain). Circulating THCs were quantified by spectral flow cytometry, and plasma sICs concentrations were determined using multiplex immunoassays. Patients were stratified by metastatic status and survival. Variables showing the strongest discriminative capacity were integrated into multivariable logistic regression models. Number of THCs, and levels of sCTLA-4, s-41BB, sLAG-3, and sTIM-3 exhibited the strongest discrimination for metastasis, while THCs, sLAG-3, and sTIM-3 distinguished deceased from surviving patients. Integrating predictive models demonstrated high accuracy, and survival analyses supported their prognostic significance. These findings indicate circulating THCs and selected sICs represent promising liquid biomarkers for monitoring lung cancer progression and patient outcomes.

Indexed as

Biomarkers, TumorImmune Checkpoint ProteinsLung NeoplasmsNeoplastic Cells, CirculatingNeoplastic Stem CellsAgedDisease ProgressionFemaleHumansMaleMiddle AgedNeoplasm MetastasisPrognosisBiomarkers, TumorImmune Checkpoint Proteinsbiomarkerlung cancersoluble immune checkpointstumour hybrid cells

Identifiers

PMID41752130
PMCPMC12940895

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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.