Evidence map›Paper›PMID 42409797›Full record

ArticleNature communications2026

Statescope: an integrative deconvolution framework for discovering cell states in tumors.

Jurriaan Janssen, Mischa F B Steketee, Aryamaan Bose, Saskia van Asten, Paul P Eijk, Frederike Dijk, Arantza Farina Sarasqueta, Febe van Maldegem, David P Noske, Idris Bahce and 7 more

Abstract read
In one paragraph

Article in Nature communications, 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

17 authors.

Jurriaan Janssen *Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-2536-7864
Mischa F B Steketee *Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-7138-7554
Aryamaan BoseAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Saskia van AstenAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Paul P EijkAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Frederike DijkAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-3970-6601
Arantza Farina SarasquetaAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-4307-1568
Febe van MaldegemAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Molecular Cell Biology and Immunology, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-2544-544X
David P NoskeAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Neurosurgery, Amsterdam, The Netherlands.
Idris BahceAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pulmonary Medicine, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-1111-608X
Jan KosterAmsterdam UMC, Vrije Universiteit Amsterdam, Laboratory of Experimental Oncology and Radiobiology, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-0890-7585
Juan J Garcia VallejoAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Molecular Cell Biology and Immunology, Amsterdam, The Netherlands.
Richard SchoonhovenAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-3659-929X
Mark A van de WielAmsterdam UMC, Vrije Universiteit Amsterdam, Department of Epidemiology & Data Science, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0003-4780-8472
Teodora Radonic *Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.
Bauke Ylstra *Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9479-3010
Yongsoo Kim *Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands. yo.kim@amsterdamumc.nl.ORCID http://orcid.org/0000-0002-2995-2131

Funding

Korea Health Industry Development Institute (KHIDI) RS-2024-00406488KWF Kankerbestrijding (Dutch Cancer Society) KWF-13774
6 · The paper itself

Abstract

Accurate deconvolution of cell states from bulk tumor RNA-seq is hindered by heterogeneous malignant cells specifically in cancer applications. We present Statescope, a Bayesian framework that incorporates DNA-derived malignant cell purity to overcome this heterogeneity and explicitly models inter-sample variation to accurately identify cell states. Comprehensive benchmarking shows Statescope outperforms existing methods in both cell fraction and state estimation, and is unique in its ability to identify states entirely absent from single-cell references. In real-data applications, Statescope successfully recapitulates established cell states, including multiple states in neutrophils, a cell type often missed by single-cell methods in lung cancer. Critically, in the POPLAR/OAK clinical trials, Statescope identifies a combinatorial signature of effector CD8 + T cells and conventional dendritic cell states that together predict a striking survival benefit from immunotherapy. Collectively, Statescope transforms deconvolution into a versatile discovery platform, enabling deeper biological and clinical insights from widely available bulk multi-omics data.

Indexed as

Lung NeoplasmsNeoplasmsBayes TheoremCD8-Positive T-LymphocytesDendritic CellsHumansNeutrophilsRNA-SeqSingle-Cell AnalysisSingle-Cell Gene Expression Analysis

Identifiers

PMID42409797
PMCPMC13478200

What Socratic holds

Textmetadata
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.