Evidence map›Paper›PMID 30003321›Full record

ReviewCancer immunology, immunotherapy : CII2019

Interactions among myeloid regulatory cells in cancer.

Viktor Umansky, Gosse J Adema, Jaroslaw Baran, Sven Brandau, Jo A Van Ginderachter, Xiaoying Hu, Jadwiga Jablonska, Slavko Mojsilovic, Helen A Papadaki, Yago Pico de Coaña and 7 more

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

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  15. Regulation of prognosis-related Siglecs in the glioma microenvironment.Journal of cancer research and clinical oncology · 2021
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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

17 authors at 11 institutions in 10 countries.

Viktor UmanskySkin Cancer Unit (G300), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany. V.Umansky@dkfz-heidelberg.de.ORCID http://orcid.org/0000-0003-0259-1839
Gosse J AdemaRadiotherapy and OncoImmunology Laboratory, Department of Radiation Oncology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
Jaroslaw BaranDepartment of Clinical Immunology, Institute of Paediatrics, Jagiellonian University Medical College, Kraków, Poland.
Sven BrandauDepartment of Otorhinolaryngology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Jo A Van GinderachterLab of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
Xiaoying HuSkin Cancer Unit (G300), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Jadwiga JablonskaDepartment of Otorhinolaryngology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Slavko MojsilovicLaboratory for Experimental Hematology and Stem Cells, Institute for Medical Research, University of Belgrade, Belgrade, Republic of Serbia.
Helen A PapadakiDepartment of Hematology, School of Medicine, University of Crete, Heraklion, Greece.
Yago Pico de CoañaDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Kim C M SantegoetsRadiotherapy and OncoImmunology Laboratory, Department of Radiation Oncology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
Juan F SantibanezDepartment of Molecular Oncology, Institute for Medical Research, University of Belgrade, Belgrade, Republic of Serbia.
Karine SerreFaculty of Medicine, Institute of Molecular Medicine (IMM)-João Lobo Antunes, University of Lisbon, Lisbon, Portugal.
Yu SiDepartment of Otorhinolaryngology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Isabela SieminskaDepartment of Clinical Immunology, Institute of Paediatrics, Jagiellonian University Medical College, Kraków, Poland.
Maria VelegrakiDepartment of Hematology, School of Medicine, University of Crete, Heraklion, Greece.
Zvi G FridlenderInstitute of Pulmonary Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
University of Duisburg-Essen · DEJagiellonian University · PLRadboud University Nijmegen · NLUniversity of Belgrade · RSUniversity of Crete · GRGerman Cancer Research Center · DEHadassah Medical Center · ILKarolinska Institutet · SEUniversity of Lisbon · PTUniversity of Mannheim · DEVrije Universiteit Brussel · BE

Funding

DKFZ-MOST Cooperation in Cancer Research CA181Horizon 2020 Framework Programme COST Action BM1404Horizon 2020 Framework Programme COST Action BM1404 Mye-EUNITER
6 · The paper itself

Abstract

Mounting evidence has accumulated on the critical role of the different myeloid cells in the regulation of the cancerous process, and in particular in the modulation of the immune reaction to cancer. Myeloid cells are a major component of host cells infiltrating tumors, interacting with each other, with tumor cells and other stromal cells, and demonstrating a prominent plasticity. We describe here various myeloid regulatory cells (MRCs) in mice and human as well as their relevant therapeutic targets. We first address the role of the monocytes and macrophages that can contribute to angiogenesis, immunosuppression and metastatic dissemination. Next, we discuss the differential role of neutrophil subsets in tumor development, enhancing the dual and sometimes contradicting role of these cells. A heterogeneous population of immature myeloid cells, MDSCs, was shown to be generated and accumulated during tumor progression as well as to be an important player in cancer-related immune suppression. Lastly, we discuss the role of myeloid DCs, which can either contribute to effective anti-tumor responses or play a more regulatory role. We believe that MRCs play a critical role in cancer-related immune regulation and suggest that future anti-cancer therapies will focus on these abundant cells.

Indexed as

AnimalsBiomarkersCell CommunicationDendritic CellsHumansMacrophagesMonocytesMyeloid CellsMyeloid-Derived Suppressor CellsNeoplasmsNeutrophilsBiomarkersDendritic cellsMacrophagesMye-EUNITERMyeloid-derived suppressor cellsMyeloid regulatory cellsNeutrophils

Identifiers

PMID30003321
PMCPMC11028297
OpenAlexW2864371843

What OpenQuestion holds

Textmetadata
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.