Evidence map›Paper›PMID 27595232›Full record

ArticleNature immunology2016

The mucin MUC1 modulates the tumor immunological microenvironment through engagement of the lectin Siglec-9.

Richard Beatson, Virginia Tajadura-Ortega, Daniela Achkova, Gianfranco Picco, Theodora-Dorita Tsourouktsoglou, Sandra Klausing, Matthew Hillier, John Maher, Thomas Noll, Paul R Crocker and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 222 papers.

0numbers the graph read from it
0cells of the map it votes in
222citing papers in PubMed
11.7field-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

222 citing papers in PubMed, 381 citations in OpenAlex.

  1. Trial
  2. Sialic acidOncoimmunology · 2026
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  17. Chemoradiotherapy facilitates siglec-10Cancer immunology, immunotherapy : CII · 2026
    Article
  18. Article
  19. Review
  20. Article

162 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

12 authors at 5 institutions in 2 countries.

Richard BeatsonBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Virginia Tajadura-OrtegaBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Daniela AchkovaCAR Mechanics Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Gianfranco PiccoBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Theodora-Dorita TsourouktsoglouBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Sandra KlausingCell Culture Technology Group, University of Bielefeld, Bielefeld, Germany.
Matthew HillierBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
John MaherCAR Mechanics Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Thomas NollCell Culture Technology Group, University of Bielefeld, Bielefeld, Germany.
Paul R CrockerSchool of Life Sciences, University of Dundee, Dundee, UK.
Joyce Taylor-PapadimitriouBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Joy M BurchellBreast Cancer Biology Group, Division of Cancer Studies, King's College London, Guy's Hospital, London, UK.
Guy's Hospital · GBKing's College London · GBBielefeld University · DEBreast Cancer Now · GBUniversity of Dundee · GB

Funding

Breast Cancer Now 2011NOVPR43Medical Research Council MR/J007196/1
6 · The paper itself

Abstract

Siglec-9 is a sialic-acid-binding lectin expressed predominantly on myeloid cells. Aberrant glycosylation occurs in essentially all types of cancers and results in increased sialylation. Thus, when the mucin MUC1 is expressed on cancer cells, it is decorated by multiple short, sialylated O-linked glycans (MUC1-ST). Here we found that this cancer-specific MUC1 glycoform, through engagement of Siglec-9, 'educated' myeloid cells to release factors associated with determination of the tumor microenvironment and disease progression. Moreover, MUC1-ST induced macrophages to display a tumor-associated macrophage (TAM)-like phenotype, with increased expression of the checkpoint ligand PD-L1. Binding of MUC1-ST to Siglec-9 did not activate the phosphatases SHP-1 or SHP-2 but, unexpectedly, induced calcium flux that led to activation of the kinases MEK-ERK. This work defines a critical role for aberrantly glycosylated MUC1 and identifies an activating pathway that follows engagement of Siglec-9.

Indexed as

Antigens, CDBiomarkersCell DifferentiationCell LineDendritic CellsExtracellular Signal-Regulated MAP KinasesGene ExpressionGlycosylationHumansMacrophagesMitogen-Activated Protein KinasesMucin-1Myeloid CellsNeoplasmsPhenotypeProtein BindingAntigens, CDBiomarkersExtracellular Signal-Regulated MAP KinasesMitogen-Activated Protein KinasesMucin-1Sialic Acid Binding Immunoglobulin-like LectinsSIGLEC9 protein, human

Identifiers

PMID27595232
PMCPMC5257269
OpenAlexW2516359951

What OpenQuestion holds

Textmetadata
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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.