Evidence map›Paper›PMID 30397348›Full record

ArticleNature immunology2018

Tumor immunoevasion via acidosis-dependent induction of regulatory tumor-associated macrophages.

Toszka Bohn, Steffen Rapp, Natascha Luther, Matthias Klein, Till-Julius Bruehl, Nobuhiko Kojima, Pamela Aranda Lopez, Jennifer Hahlbrock, Sabine Muth, Shogo Endo and 19 more

Abstract read
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In one paragraph

Article in Nature immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 242 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
242citing papers in PubMed, 1 pooled it
13.5field-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

242 citing papers in PubMed, 1 synthesis or guideline pooled it, 428 citations in OpenAlex.

  1. Pooled it
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  15. Obesity Disrupts H3K4me3-Mediated Lactate Accumulation and Efferocytosis in Hypoxic Macrophages.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  17. CAR-macrophages: a new chapter in cancer immunotherapy.Acta biochimica et biophysica Sinica · 2026
    Article
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182 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 9 institutions in 4 countries.

Toszka BohnInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Steffen RappMolecular Genetics, Johannes Gutenberg University Mainz, Mainz, Germany.
Natascha LutherDermatology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Matthias KleinInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Till-Julius BruehlInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Nobuhiko KojimaFaculty of Life Sciences, Toyo University, Gunma, Japan.
Pamela Aranda LopezThird Medical Clinic, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Jennifer HahlbrockInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Sabine MuthInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Shogo EndoAging Neuroscience Research Team, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Stefanie PektorDepartment of Nuclear Medicine, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Almut BrandInternal Medicine III, University of Regensburg, Regensburg, Germany.
Kathrin RennerInternal Medicine III, University of Regensburg, Regensburg, Germany.
Vanessa PoppDepartment of Medicine 1, University of Erlangen-Nürnberg, Erlangen, Germany.
Katharina GerlachDepartment of Medicine 1, University of Erlangen-Nürnberg, Erlangen, Germany.
Dennis VogelInstitute for Medical Microbiology and Hospital Hygiene, University of Marburg, Marburg, Germany.
Christina LueckelInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Danielle Arnold-SchildInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Jacques PouyssegurInstitute of Research on Cancer and Aging, University of Nice-Sophia Antipolis, Nice, France.
Marina KreutzInternal Medicine III, University of Regensburg, Regensburg, Germany.
Magdalena HuberInstitute for Medical Microbiology and Hospital Hygiene, University of Marburg, Marburg, Germany.
Jochem KoenigInstitute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.
Benno WeigmannDepartment of Medicine 1, University of Erlangen-Nürnberg, Erlangen, Germany.
Hans-Christian ProbstInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Esther von StebutDermatology and Venereology, University Medical Center Cologne, Cologne, Germany.
Christian BeckerDermatology, University Medical Center, Johannes Gutenberg-University Mainz, Mainz, Germany.ORCID http://orcid.org/0000-0002-1716-7208
Hansjoerg SchildInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Edgar SchmittInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Tobias BoppInstitute for Immunology, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany. boppt@uni-mainz.de.ORCID http://orcid.org/0000-0002-3232-8065
Johannes Gutenberg University Mainz · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEPhilipps University of Marburg · DEUniversity of Regensburg · DEGerman Cancer Research Center · DEInstitut de Recherche sur le Cancer et le Vieillissement de Nice · FRTokyo Metropolitan Institute of Gerontology · JPToyo University · JPUniversity Hospital Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many tumors evolve sophisticated strategies to evade the immune system, and these represent major obstacles for efficient antitumor immune responses. Here we explored a molecular mechanism of metabolic communication deployed by highly glycolytic tumors for immunoevasion. In contrast to colon adenocarcinomas, melanomas showed comparatively high glycolytic activity, which resulted in high acidification of the tumor microenvironment. This tumor acidosis induced Gprotein-coupled receptor-dependent expression of the transcriptional repressor ICER in tumor-associated macrophages that led to their functional polarization toward a non-inflammatory phenotype and promoted tumor growth. Collectively, our findings identify a molecular mechanism of metabolic communication between non-lymphoid tissue and the immune system that was exploited by high-glycolytic-rate tumors for evasion of the immune system.

Indexed as

AcidosisAdenocarcinomaAnimalsColonic NeoplasmsGlycolysisHumansMacrophagesMelanomaMiceMice, Inbred C57BLMice, TransgenicTumor EscapeTumor Microenvironment

Identifiers

PMID30397348
OpenAlexW2898195249

What OpenQuestion holds

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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.