Evidence map›Paper›PMID 29910806›Full record

ArticleFrontiers in immunology2018

Targeting the Epidermal Growth Factor Receptor Can Counteract the Inhibition of Natural Killer Cell Function Exerted by Colorectal Tumor-Associated Fibroblasts.

Delfina Costa, Roberta Venè, Roberto Benelli, Emanuele Romairone, Stefano Scabini, Silvia Catellani, Barbara Rebesco, Luca Mastracci, Federica Grillo, Simona Minghelli and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  4. Medulloblastoma: biology and immunotherapy.Frontiers in immunology · 2025
    Review
  5. Article
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  7. Review
  8. NK cells direct the perspective approaches to cancer immunotherapy.Medical oncology (Northwood, London, England) · 2023
    Review
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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

13 authors at 3 institutions in 1 country.

Delfina CostaMolecular Oncology and Angiogenesis Unit, Ospedale Policlinico San Martino, Genoa, Italy.
Roberta VenèMolecular Oncology and Angiogenesis Unit, Ospedale Policlinico San Martino, Genoa, Italy.
Roberto BenelliImmunology Unit, Ospedale Policlinico San Martino, Genoa, Italy.
Emanuele RomaironeOncological Surgery, Ospedale Policlinico San Martino, Genoa, Italy.
Stefano ScabiniOncological Surgery, Ospedale Policlinico San Martino, Genoa, Italy.
Silvia CatellaniClinical Hematology, Ospedale Policlinico San Martino, Genoa, Italy.
Barbara RebescoAntiblastic Drug Unit, Ospedale Policlinico San Martino, Genoa, Italy.
Luca MastracciUnit of Pathology, Ospedale Policlinico San Martino, Genoa, Italy.
Federica GrilloUnit of Pathology, Ospedale Policlinico San Martino, Genoa, Italy.
Simona MinghelliClinical and Experimental Immunology Laboratory, Ospedale G. Gaslini, Genoa, Italy.
Fabrizio LoiaconoImmunology Unit, Ospedale Policlinico San Martino, Genoa, Italy.
Maria Raffaella ZocchiDivision of Immunology, Transplants and Infectious Diseases, San Raffaele Scientific Institute, Milan, Italy.
Alessandro PoggiMolecular Oncology and Angiogenesis Unit, Ospedale Policlinico San Martino, Genoa, Italy.
Ospedale Policlinico San Martino · ITIstituto Giannina Gaslini · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stromal cells (MSC) present in the tumor microenvironment [usually named tumor-associated fibroblasts (TAF)] can exert immunosuppressive effects on T and natural killer (NK) lymphocytes, favoring tumor immune escape. We have analyzed this mechanism in colorectal carcinoma (CRC) and found that co-culture of NK cells with TAF can prevent the IL-2-mediated NKG2D upregulation. This leads to the impairment of NKG2D-mediated recognition of CRC cells, sparing the NK cell activation through DNAM1 or FcγRIIIA (CD16).

Indexed as

Antineoplastic Agents, ImmunologicalCancer-Associated FibroblastsCell CommunicationCell Line, TumorCetuximabCoculture TechniquesColorectal NeoplasmsCytotoxicity, ImmunologicErbB ReceptorsHumansKiller Cells, NaturalLymphokinesAntineoplastic Agents, ImmunologicalCetuximabErbB ReceptorsLymphokinest cell-activating lymphokineantibody-dependent cellular cytotoxicitycetuximabCRCEGFRnatural killer cellsNKG2DTME

Identifiers

PMID29910806
PMCPMC5992415
OpenAlexW2805701467

What OpenQuestion holds

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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.