Evidence map›Paper›PMID 37188691›Full record

ArticleNature communications2023

Extracellular matrix educates an immunoregulatory tumor macrophage phenotype found in ovarian cancer metastasis.

E H Puttock, E J Tyler, M Manni, E Maniati, C Butterworth, M Burger Ramos, E Peerani, P Hirani, V Gauthier, Y Liu and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
15.6field-weighted citation impact, top 1% of its field
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

76 citing papers in PubMed, 93 citations in OpenAlex.

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16 more citing papers are in PubMed but not listed here.

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

20 authors at 4 institutions in 3 countries.

E H Puttock *Queen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0002-2804-8247
E J Tyler *Queen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0001-8945-4823
M ManniDepartment of Biomedicine and Division of Medical Oncology, University Hospital Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
E ManiatiQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0001-6993-9890
C ButterworthQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0002-9416-6057
M Burger RamosQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.
E PeeraniQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0003-0801-5568
P HiraniQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.
V GauthierQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0001-7360-4305
Y LiuQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.
G ManiscalcoQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.
V RajeeveQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0002-6361-4291
P CutillasQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0002-3426-2274
C TrevisanDepartment of Women and Children Health, University of Padova and Fondazione Istituto di Ricerca Pediatrica Città della Speranza, Corso Stati Uniti 4, 35127, Padova, Italy.
M PozzobonDepartment of Women and Children Health, University of Padova and Fondazione Istituto di Ricerca Pediatrica Città della Speranza, Corso Stati Uniti 4, 35127, Padova, Italy.
M LockleyQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK.ORCID 0000-0002-9281-5789
J RastrickUCB Pharma Ltd, 208 Bath Road, Slough, Berkshire, SL1 3WE, UK.
H LäubliDepartment of Biomedicine and Division of Medical Oncology, University Hospital Basel, Hebelstrasse 20, 4031, Basel, Switzerland.ORCID 0000-0002-8910-5620
A WhiteUCB Pharma Ltd, 208 Bath Road, Slough, Berkshire, SL1 3WE, UK.
O M T PearceQueen Mary University of London, Barts Cancer Institute, John Vane Science Centre, London, EC1M 6BQ, UK. o.pearce@qmul.ac.uk.ORCID 0000-0003-3953-1629
Queen Mary University of London · GBCittà della Speranza Foundation · ITUCB Pharma (United Kingdom) · GBUniversity Hospital of Basel · CH

Funding

Cancer Research UK 27947
6 · The paper itself

Abstract

Recent studies have shown that the tumor extracellular matrix (ECM) associates with immunosuppression, and that targeting the ECM can improve immune infiltration and responsiveness to immunotherapy. A question that remains unresolved is whether the ECM directly educates the immune phenotypes seen in tumors. Here, we identify a tumor-associated macrophage (TAM) population associated with poor prognosis, interruption of the cancer immunity cycle, and tumor ECM composition. To investigate whether the ECM was capable of generating this TAM phenotype, we developed a decellularized tissue model that retains the native ECM architecture and composition. Macrophages cultured on decellularized ovarian metastasis shared transcriptional profiles with the TAMs found in human tissue. ECM-educated macrophages have a tissue-remodeling and immunoregulatory phenotype, inducing altered T cell marker expression and proliferation. We conclude that the tumor ECM directly educates this macrophage population found in cancer tissues. Therefore, current and emerging cancer therapies that target the tumor ECM may be tailored to improve macrophage phenotype and their downstream regulation of immunity.

Indexed as

MacrophagesOvarian NeoplasmsExtracellular MatrixFemaleHumansPhenotypeTumor Microenvironment

Identifiers

PMID37188691
PMCPMC10185550
OpenAlexW4376612447

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.