Evidence map›Paper›PMID 32601464›Full record

ArticleBritish journal of cancer2020

EGFR/Ras-induced CCL20 production modulates the tumour microenvironment.

Andreas Hippe, Stephan Alexander Braun, Péter Oláh, Peter Arne Gerber, Anne Schorr, Stephan Seeliger, Stephanie Holtz, Katharina Jannasch, Andor Pivarcsi, Bettina Buhren and 19 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 41 citations in OpenAlex.

  1. Prognostic significance of pre-intervention circulating cytokines in digestive system cancers: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  9. CCL20 in the tumor microenvironment: implications for cancer progression and therapeutic approaches.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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  16. Crosstalk between purinergic receptor P2YCellular and molecular life sciences : CMLS · 2024
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  20. [Lnc-TMEM132D-AS1 overexpression reduces sensitivity of non-small cell lung cancer cells to osimertinib].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 13 institutions in 6 countries.

Andreas Hippe *Department of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Stephan Alexander Braun *Department of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Péter OláhDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Peter Arne GerberDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Anne SchorrDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Stephan SeeligerDepartment of Pediatric Cardiology and Intensive Care Medicine, Medical Center Georg August University Göttingen, Göttingen, Germany.
Stephanie HoltzDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Katharina JannaschClinic of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.
Andor PivarcsiDermatology and Venereology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Bettina BuhrenDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Holger SchrumpfDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Andreas KislatDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Erich BünemannDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Martin SteinhoffDepartment of Dermatology and UCD Charles Institute for Dermatology, University College Dublin, Dublin, Ireland.
Jens FischerDepartment of Pharmacology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Sérgio A LiraPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Petra BoukampLeibnitz Research Institute for Environmental Medicine, Düsseldorf, Germany.
Peter HeveziDepartment of Physiology and Biophysics, University of California, Irvine, CA, USA.
Nikolas Hendrik StoeckleinDepartment of General-, Visceral- and Pediatric Surgery, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Thomas HoffmannDepartment of Otorhinolaryngology, Head and Neck Surgery, University Medical Center, Ulm, Germany.
Frauke AlvesClinic of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.
Jonathan SleemanEuropean Center for Angioscience (ECAS), Medical Faculty of Mannheim, Heidelberg University, Mannheim, Germany.
Thomas BauerInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna and Comprehensive Cancer Center, Vienna, Austria.
Jörg KlufaInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna and Comprehensive Cancer Center, Vienna, Austria.
Nicole AmbergInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna and Comprehensive Cancer Center, Vienna, Austria.
Maria SibiliaInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna and Comprehensive Cancer Center, Vienna, Austria.
Albert ZlotnikInsitute for Immunology, University of California, Irvine, CA, USA.
Anja Müller-HomeyDepartment of Radiation Oncology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Bernhard HomeyDepartment of Dermatology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany. Bernhard.Homey@med.uni-duesseldorf.de.
Heinrich Heine University Düsseldorf · DEComprehensive Cancer Center Vienna · ATUniversitätsmedizin Göttingen · DEUniversity of California, Irvine · USIcahn School of Medicine at Mount Sinai · USInstitute of Science and Technology Austria · ATKarlsruhe Institute of Technology · DEKarolinska Institutet · SELeibniz Institute of Environmental Medicine · DEUniversity College Dublin · IEUniversity Hospital Münster · DEUniversity Hospital Ulm · DEUniversity of Göttingen · DE

Funding

Mechanisms associated with flares and remission in colitisR01DK110352 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2017 to 2025
$5.1M
Molecular pathogenesis of intestinal serrated polypsR01CA161373 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2011 to 2020
$3.7M
Mechanisms associated with diet-induced colitisR01DK121009 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2020 to 2023
$2.4M
Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) I4300-BAustrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) W1212Austrian Science Fund FWF I 4300Deutsche Forschungsgemeinschaft (German Research Foundation) HO 2092/8-1Deutsche Forschungsgemeinschaft (German Research Foundation) SPP1190NCI NIH HHS R01 CA161373Vienna Science and Technology Fund (Wiener Wissenschafts-, Forschungs- und Technologiefonds) LS16-025
6 · The paper itself

Abstract

backgroundThe activation of the EGFR/Ras-signalling pathway in tumour cells induces a distinct chemokine repertoire, which in turn modulates the tumour microenvironment.

methodsThe effects of EGFR/Ras on the expression and translation of CCL20 were analysed in a large set of epithelial cancer cell lines and tumour tissues by RT-qPCR and ELISA in vitro. CCL20 production was verified by immunohistochemistry in different tumour tissues and correlated with clinical data. The effects of CCL20 on endothelial cell migration and tumour-associated vascularisation were comprehensively analysed with chemotaxis assays in vitro and in CCR6-deficient mice in vivo.

resultsTumours facilitate progression by the EGFR/Ras-induced production of CCL20. Expression of the chemokine CCL20 in tumours correlates with advanced tumour stage, increased lymph node metastasis and decreased survival in patients. Microvascular endothelial cells abundantly express the specific CCL20 receptor CCR6. CCR6 signalling in endothelial cells induces angiogenesis. CCR6-deficient mice show significantly decreased tumour growth and tumour-associated vascularisation. The observed phenotype is dependent on CCR6 deficiency in stromal cells but not within the immune system.

conclusionWe propose that the chemokine axis CCL20-CCR6 represents a novel and promising target to interfere with the tumour microenvironment, and opens an innovative multimodal strategy for cancer therapy.

Indexed as

Tumor MicroenvironmentAnimalsCells, CulturedChemokine CCL20ErbB ReceptorsExtracellular Signal-Regulated MAP KinasesHumansMaleMiceMice, Inbred C57BLNeoplasmsNeoplasm StagingNeovascularization, Pathologicras ProteinsReceptors, CCR6Signal TransductionChemokine CCL20ErbB ReceptorsExtracellular Signal-Regulated MAP Kinasesras ProteinsReceptors, CCR6

Identifiers

PMID32601464
PMCPMC7493992
OpenAlexW3037249938

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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.