Evidence map›Paper›PMID 40627458›Full record

ArticleJCI insight2025

Tumor microenvironments with an active type I IFN response are sensitive to inhibitors of heme degradation.

Dominika Sosnowska, Tik Shing Cheung, Jit Sarkar, James W Opzoomer, Karen T Feehan, Joanne E Anstee, Chloé A Woodman, Mohamed Reda Keddar, Kalum Clayton, Samira Ali and 9 more

Abstract read
In one paragraph

Article in JCI insight, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

19 authors.

Dominika SosnowskaSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Tik Shing CheungSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Jit SarkarSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
James W OpzoomerSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Karen T FeehanSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Joanne E AnsteeSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Chloé A WoodmanSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Mohamed Reda KeddarCancer Systems Biology Laboratory, The Francis Crick Institute, London, United Kingdom.
Kalum ClaytonCancer Systems Biology Laboratory, The Francis Crick Institute, London, United Kingdom.
Samira AliSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
William MacmorlandSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Dorothy D YangSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
James RosekillySchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Cheryl E GillettSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Francesca D CiccarelliCancer Systems Biology Laboratory, The Francis Crick Institute, London, United Kingdom.
Richard BuusThe Breast Cancer Now Toby Robins Research Centre at The Institute of Cancer Research, London, United Kingdom.
James SpicerSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
Anita GrigoriadisSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.
James N ArnoldSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor microenvironment (TME) is highly heterogeneous and can dictate the success of therapeutic interventions. Identifying TMEs that are susceptible to specific therapeutic interventions paves the way for more personalized and effective treatments. In this study, using a spontaneous murine model of breast cancer, we characterize a TME that is responsive to inhibitors of the heme degradation pathway mediated by heme oxygenase (HO), resulting in CD8+ T cell- and NK cell-dependent tumor control. A hallmark of this TME is a chronic type I interferon (IFN) signal that is directly involved in orchestrating the antitumor immune response. Importantly, we identify that similar TMEs exist in human breast cancer that are associated with patient prognosis. Leveraging these observations, we demonstrate that combining a STING agonist, which induces type I IFN responses, with an HO inhibitor produces a synergistic effect leading to superior tumor control. This study highlights HO activity as a potential resistance mechanism for type I IFN responses in cancer, supporting a therapeutic rationale for targeting the heme degradation pathway to enhance the efficacy of STING agonists.

Indexed as

Breast NeoplasmsHemeHeme Oxygenase (Decyclizing)Interferon Type ITumor MicroenvironmentAnimalsCD8-Positive T-LymphocytesCell Line, TumorDisease Models, AnimalFemaleHumansKiller Cells, NaturalMembrane ProteinsMiceSignal TransductionSTING ProteinHemeHeme Oxygenase (Decyclizing)Interferon Type IMembrane ProteinsSting1 protein, mouseSTING ProteinBreast cancerCancer immunotherapyImmunologyImmunotherapyOncology

Identifiers

PMID40627458
PMCPMC12406722

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Registered trials

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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.