Evidence map›Paper›PMID 32449776›Full record

ReviewInternational immunology2020

Role of dendritic cell metabolic reprogramming in tumor immune evasion.

Michael P Plebanek, Michael Sturdivant, Nicholas C DeVito, Brent A Hanks

Abstract readReview
In one paragraph

Review in International immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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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

4 authors.

Michael P Plebanek
Michael Sturdivant
Nicholas C DeVito
Brent A Hanks

Funding

Melanoma-mediated Dendritic Cell Tolerization and Immune EvasionK08CA191063 · NCI · DUKE UNIVERSITY · PI HANKS, BRENT ALLEN · 2015 to 2019
$826k
NCI NIH HHS K08 CA191063
6 · The paper itself

Abstract

The dendritic cell (DC) is recognized as a vital mediator of anti-tumor immunity. More recent studies have also demonstrated the important role of DCs in the generation of effective responses to checkpoint inhibitor immunotherapy. Metabolic programming of DCs dictates their functionality and can determine which DCs become immunostimulatory versus those that develop a tolerized phenotype capable of actively suppressing effector T-cell responses to cancers. As a result, there is great interest in understanding what mechanisms have evolved in cancers to alter these metabolic pathways, thereby allowing for their continued progression and metastasis. The therapeutic strategies developed to reverse these processes of DC tolerization in the tumor microenvironment represent promising candidates for future testing in combination immunotherapy clinical trials.

Indexed as

AnimalsDendritic CellsHumansImmunotherapyNeoplasmsTumor Microenvironment3-dioxygenasefatty acid oxidationindoleamine 2lipid bodiesPPARβ-catenin

Identifiers

PMID32449776
PMCPMC7318778

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.