Evidence map›Paper›PMID 28546500›Full record

ReviewJournal of leukocyte biology2017

Myeloid-derived suppressor cells-a new therapeutic target to overcome resistance to cancer immunotherapy.

Jason A Chesney, Robert A Mitchell, Kavitha Yaddanapudi

Abstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
–field-weighted citation impact
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

79 citing papers in PubMed.

  1. Review
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  17. Article
  18. Tumor-associated myeloid cells in cancer immunotherapy.Journal of hematology & oncology · 2023
    Review
  19. Article
  20. Review

19 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

3 authors.

Jason A ChesneyMolecular Targets Program, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA; robert.mitchell@louisville.edu kavitha.yaddanapudi@louisville.edu.
Robert A MitchellMolecular Targets Program, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA; robert.mitchell@louisville.edu.
Kavitha YaddanapudiMolecular Targets Program, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, USA; kavitha.yaddanapudi@louisville.edu.

Funding

PILOT PROJECT PROGRAMP30GM106396 · NIGMS · UNIVERSITY OF LOUISVILLE · PI EATON, JOHN W · 2013 to 2017
$5.4M
Small molecule targeting of MIF as a novel melanoma therapeuticR01CA186661 · NCI · UNIVERSITY OF LOUISVILLE · PI MITCHELL, ROBERT A · 2014 to 2018
$1.6M
Activation of Cyclin-Dependent Kinases by Fructose-2,6-BisphosphateR01CA149438 · NCI · UNIVERSITY OF LOUISVILLE · PI CHESNEY, JASON A. · 2011 to 2015
$1.5M
Role of MIF in Rb inactivation and TumorigenesisR01CA102285 · NCI · UNIVERSITY OF LOUISVILLE · PI MITCHELL, ROBERT A · 2004 to 2009
$1.4M
NCI NIH HHS R01 CA102285NCI NIH HHS R01 CA149438NCI NIH HHS R01 CA186661NIGMS NIH HHS P30 GM106396
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of immature myeloid cells that accumulate during pathologic conditions, such as cancer. Patients diagnosed with advanced metastatic cancers have an average survival of 12-24 mo, a survival time that hasn't changed significantly in the past 30 yr. Despite some encouraging improvements in response rates and overall survival in patients receiving immunotherapies, such as immune checkpoint inhibitors, most patients will ultimately progress. MDSCs contribute to immunotherapeutic resistance by actively inhibiting antitumor T cell proliferation and cytotoxic activity as well as by promoting expansion of protumorigenic T regulatory cells, thereby, dampening the host immune responses against the tumor. In addition, MDSCs promote angiogenesis, tumor invasion, and metastasis. Thus, MDSCs are potential therapeutic targets in cases of multiple cancers. This review focuses on the phenotypic and functional characteristics of MDSCs and provides an overview of the mono- and combinatorial-therapeutic strategies that target MDSCs with an objective of enhancing the efficacy of cancer immunotherapies.

Indexed as

AnimalsCell ProliferationHumansImmunotherapyMyeloid-Derived Suppressor CellsNeoplasm MetastasisNeoplasmsT-Lymphocytes, Regulatoryimmune checkpoint inhibitorsimmune suppressionMDSCMIFPFKFB3tumor immunology

Identifiers

PMID28546500
PMCPMC6608049

What OpenQuestion holds

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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.