Evidence map›Paper›PMID 33378668›Full record

ArticleCell reports2020

Distinct Populations of Immune-Suppressive Macrophages Differentiate from Monocytic Myeloid-Derived Suppressor Cells in Cancer.

Taekyoung Kwak, Fang Wang, Hui Deng, Thomas Condamine, Vinit Kumar, Michela Perego, Andrew Kossenkov, Luis J Montaner, Xiaowei Xu, Wei Xu and 12 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

133 citing papers in PubMed, 172 citations in OpenAlex.

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73 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

22 authors at 4 institutions in 2 countries.

Taekyoung KwakThe Wistar Institute, Philadelphia, PA 19104, USA.
Fang WangThe Wistar Institute, Philadelphia, PA 19104, USA.
Hui DengThe Wistar Institute, Philadelphia, PA 19104, USA.
Thomas CondamineThe Wistar Institute, Philadelphia, PA 19104, USA.
Vinit KumarThe Wistar Institute, Philadelphia, PA 19104, USA.
Michela PeregoThe Wistar Institute, Philadelphia, PA 19104, USA.
Andrew KossenkovThe Wistar Institute, Philadelphia, PA 19104, USA.
Luis J MontanerThe Wistar Institute, Philadelphia, PA 19104, USA.
Xiaowei XuTara Miller Melanoma Center, Abramson Cancer Center and Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Wei XuTara Miller Melanoma Center, Abramson Cancer Center and Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cathy ZhengTara Miller Melanoma Center, Abramson Cancer Center and Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Lynn M SchuchterAbramson Cancer Center and Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Ravi K AmaravadiAbramson Cancer Center and Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Tara C MitchellAbramson Cancer Center and Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Giorgos C KarakousisAbramson Cancer Center and Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Charles MulliganHelen F Graham Cancer Center and Research Institute, Christiana Care, Newark, DE 19713, USA.
Brian NamHelen F Graham Cancer Center and Research Institute, Christiana Care, Newark, DE 19713, USA.
Gregory MastersHelen F Graham Cancer Center and Research Institute, Christiana Care, Newark, DE 19713, USA.
Neil HocksteinHelen F Graham Cancer Center and Research Institute, Christiana Care, Newark, DE 19713, USA.
Joseph BennettHelen F Graham Cancer Center and Research Institute, Christiana Care, Newark, DE 19713, USA.
Yulia NefedovaThe Wistar Institute, Philadelphia, PA 19104, USA.
Dmitry I GabrilovichCancer Immunology, AstraZeneca, Gaithersburg, MD 20878, USA. Electronic address: dmitry.gabrilovich@astrazeneca.com.
The Wistar Institute · USUniversity of Pennsylvania · USChristiana Care Health System · USAstraZeneca (Netherlands) · NL

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Targeting the MAP and PI3 Kinase Pathways in MelanomaP01CA114046 · NCI · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2008 to 2023
$37.1M
Correction of myeloid cell defects in cancerR01CA084488 · NCI · WISTAR INSTITUTE · PI GABRILOVICH, DMITRY I · 1999 to 2017
$5.4M
Mechanism of myeloid cell defect in cancerR01CA100062 · NCI · WISTAR INSTITUTE · PI GABRILOVICH, DMITRY I · 2004 to 2018
$4.0M
Lipids and Myeloid Cell Function in CancerR01CA165065 · NCI · WISTAR INSTITUTE · PI KAGAN, VALERIAN E, MONTANER, LUIS J · 2012 to 2022
$3.8M
Integrative Approach to Comprehensive Analysis of High Throughput Data on a Cancer Center LevelR50CA211199 · NCI · WISTAR INSTITUTE · PI Andrew V Kossenkov · 2016 to 2026
$1.6M
NCI NIH HHS P01 CA114046NCI NIH HHS P30 CA010815NCI NIH HHS R01 CA084488NCI NIH HHS R01 CA100062NCI NIH HHS R01 CA165065NCI NIH HHS R50 CA211199
6 · The paper itself

Abstract

Here, we report that functional heterogeneity of macrophages in cancer could be determined by the nature of their precursors: monocytes (Mons) and monocytic myeloid-derived suppressor cells (M-MDSCs). Macrophages that are differentiated from M-MDSCs, but not from Mons, are immune suppressive, with a genomic profile matching that of M-MDSCs. Immune-suppressive activity of M-MDSC-derived macrophages is dependent on the persistent expression of S100A9 protein in these cells. S100A9 also promotes M2 polarization of macrophages. Tissue-resident- and Mon-derived macrophages lack expression of this protein. S100A9-dependent immune-suppressive activity of macrophages involves transcription factor C/EBPβ. The presence of S100A9-positive macrophages in tumor tissues is associated with shorter survival in patients with head and neck cancer and poor response to PD-1 antibody treatment in patients with metastatic melanoma. Thus, this study reveals the pathway of the development of immune-suppressive macrophages and suggests an approach to their selective targeting.

Indexed as

Immunosuppression TherapyAdultAgedAged, 80 and overAnimalsCalgranulin ACalgranulin BCCAAT-Enhancer-Binding ProteinsCell Line, TumorFemaleHumansMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutCalgranulin ACalgranulin BCCAAT-Enhancer-Binding ProteinsC-EPB transcription factorimmune suppressionmyeloid-derived suppressor cellsS100A9tumor associated macrophagestumor immunology

Identifiers

PMID33378668
PMCPMC7809772
OpenAlexW3116206322

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.