Evidence map›Paper›PMID 34561272›Full record

ArticleCancer research2021

TGFBI Production by Macrophages Contributes to an Immunosuppressive Microenvironment in Ovarian Cancer.

Laura S M Lecker, Chiara Berlato, Eleni Maniati, Robin Delaine-Smith, Oliver M T Pearce, Owen Heath, Samuel J Nichols, Caterina Trevisan, Marian Novak, Jacqueline McDermott and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
27.9field-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

99 citing papers in PubMed, 169 citations in OpenAlex.

  1. Article
  2. Multi-omics analysis identifieTranslational cancer research · 2026
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39 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

17 authors at 5 institutions in 4 countries.

Laura S M LeckerBarts Cancer Institute, London, United Kingdom.
Chiara Berlato *Barts Cancer Institute, London, United Kingdom.
Eleni Maniati *Barts Cancer Institute, London, United Kingdom.ORCID 0000-0001-6993-9890
Robin Delaine-Smith *Barts Cancer Institute, London, United Kingdom.
Oliver M T PearceBarts Cancer Institute, London, United Kingdom.
Owen HeathBarts Cancer Institute, London, United Kingdom.ORCID 0000-0002-9447-966X
Samuel J NicholsBarts Cancer Institute, London, United Kingdom.ORCID 0000-0001-6737-0610
Caterina TrevisanFondazione Istituto di Ricerca Pediatrica Città della Speranza, Padova, Italy.
Marian NovakDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts.
Jacqueline McDermottBarts Cancer Institute, London, United Kingdom.
James D BrentonCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-5738-6683
Pedro R CutillasBarts Cancer Institute, London, United Kingdom.ORCID 0000-0002-3426-2274
Vinothini RajeeveBarts Cancer Institute, London, United Kingdom.ORCID 0000-0002-6361-4291
Ana HenninoCancer Research Center of Lyon, UMR INSERM 1052, Lyon, France.
Ronny DrapkinOvarian Cancer Research Center, Perelman School of Medicine, Philadelphia, Pennsylvania.ORCID 0000-0002-6912-6977
Daniela LoessnerBarts Cancer Institute, London, United Kingdom.ORCID 0000-0001-5891-3441
Frances R BalkwillBarts Cancer Institute, London, United Kingdom. f.balkwill@qmul.ac.uk.
Dana-Farber Cancer Institute · USInserm · FRUniversity of Cambridge · GBUniversity of Padua · ITUniversity of Pennsylvania · US

Funding

SPORE in Ovarian CancerP50CA228991 · NCI · JOHNS HOPKINS UNIVERSITY · PI Tian-Li Wang · 2018 to 2026
$20.5M
Cancer Research UK 15601Cancer Research UK 16354Cancer Research UK 22905Cancer Research UK 25714Cancer Research UK 27947Cancer Research UK A21222Cancer Research UK C16420/A18066Cancer Research UK C355/A25137Cancer Research UK C587/A16354Cancer Research UK C587/A25714NCI NIH HHS P50 CA228991Wellcome TrustWellcome Trust 201118/Z/16/Z
6 · The paper itself

Abstract

The tumor microenvironment evolves during malignant progression, with major changes in nonmalignant cells, cytokine networks, and the extracellular matrix (ECM). In this study, we aimed to understand how the ECM changes during neoplastic transformation of serous tubal intraepithelial carcinoma lesions (STIC) into high-grade serous ovarian cancers (HGSOC). Analysis of the mechanical properties of human fallopian tubes (FT) and ovaries revealed that normal FT and fimbria had a lower tissue modulus, a measure of stiffness, than normal or diseased ovaries. Proteomic analysis of the matrisome fraction between FT, fimbria, and ovaries showed significant differences in the ECM protein TGF beta induced (TGFBI, also known as βig-h3). STIC lesions in the fimbria expressed high levels of TGFBI, which was predominantly produced by CD163-positive macrophages proximal to STIC epithelial cells.

Indexed as

Tumor MicroenvironmentAnimalsApoptosisCell ProliferationCystadenocarcinoma, SerousExtracellular MatrixFemaleHumansImmunosuppressive AgentsMacrophagesMiceMice, Inbred C57BLOvarian NeoplasmsPeritoneal NeoplasmsPrognosisTransforming Growth Factor beta1Immunosuppressive AgentsTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID34561272
PMCPMC9397609
OpenAlexW3199550886

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.