Evidence map›Paper›PMID 34673569›Full record

ArticleJCI insight2021

VEGFR2 activity on myeloid cells mediates immune suppression in the tumor microenvironment.

Yuqing Zhang, Huocong Huang, Morgan Coleman, Arturas Ziemys, Purva Gopal, Syed M Kazmi, Rolf A Brekken

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

44 citing papers in PubMed, 50 citations in OpenAlex.

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  9. Targeting Tumor-Associated Macrophages and Cancer-Associated Fibroblasts to Overcome Therapeutic Resistance in Hepatocellular Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    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

7 authors at 3 institutions in 1 country.

Yuqing ZhangHamon Center for Therapeutic Oncology Research.
Huocong HuangHamon Center for Therapeutic Oncology Research.
Morgan ColemanHamon Center for Therapeutic Oncology Research.
Arturas ZiemysProgram of Mathematics in Medicine, Houston Methodist Research Institute, Houston, Texas, USA.
Purva GopalDepartment of Pathology and.
Syed M KazmiDivision of Hematology and Oncology, Department of Medicine, UT Southwestern, Dallas, Texas, USA.
Rolf A BrekkenHamon Center for Therapeutic Oncology Research.
Cancer Genetics (United States) · USSouthwestern Medical Center · USHouston Methodist · US

Funding

Transport Oncophysics CoreU54CA210181 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WANG, RONGFU · 2016 to 2020
$9.3M
Targeted inhibition in stromal TGFβ activity in pancreatic cancerR01CA243577 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI BREKKEN, ROLF A · 2020 to 2023
$1.7M
NCI NIH HHS R01 CA243577NCI NIH HHS U54 CA210181
6 · The paper itself

Abstract

Angiogenesis, a hallmark of cancer, is induced by vascular endothelial growth factor-A (hereafter VEGF). As a result, anti-VEGF therapy is commonly used for cancer treatment. Recent studies have found that VEGF expression is also associated with immune suppression in patients with cancer. This connection has been investigated in preclinical and clinical studies by evaluating the therapeutic effect of combining antiangiogenic reagents with immune therapy. However, the mechanisms of how anti-VEGF strategies enhance immune therapy are not fully understood. We and others have shown selective elevation of VEGFR2 expression on tumor-associated myeloid cells in tumor-bearing animals. Here, we investigated the function of VEGFR2+ myeloid cells in regulating tumor immunity and found VEGF induced an immunosuppressive phenotype in VEGFR2+ myeloid cells, including directly upregulating the expression of programmed cell death 1 ligand 1. Moreover, we found that VEGF blockade inhibited the immunosuppressive phenotype of VEGFR2+ myeloid cells, increased T cell activation, and enhanced the efficacy of immune checkpoint blockade. This study highlights the function of VEGFR2 on myeloid cells and provides mechanistic insight on how VEGF inhibition potentiates immune checkpoint blockade.

Indexed as

Angiogenesis InhibitorsDisease ProgressionHumansMyeloid CellsNeoplasmsTumor MicroenvironmentVascular Endothelial Growth Factor Receptor-2Angiogenesis InhibitorsVascular Endothelial Growth Factor Receptor-2Cancer immunotherapyImmunologyMacrophagesOncology

Identifiers

PMID34673569
PMCPMC8675197
OpenAlexW3205631127

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.