Evidence map›Paper›PMID 33720040›Full record

ReviewThe Journal of clinical investigation2021

Neutrophil dynamics in the tumor microenvironment.

Amanda J McFarlane, Frédéric Fercoq, Seth B Coffelt, Leo M Carlin

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
6.5field-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

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 120 citations in OpenAlex.

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  19. [Molecular Mechanism of Neutrophils Driving the Progression of Lung Adenocarcinoma].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2025
    Review
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21 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

4 authors at 1 institution in 1 country.

Amanda J McFarlaneCancer Research UK Beatson Institute, Glasgow, United Kingdom.
Frédéric FercoqCancer Research UK Beatson Institute, Glasgow, United Kingdom.
Seth B CoffeltCancer Research UK Beatson Institute, Glasgow, United Kingdom.
Leo M CarlinCancer Research UK Beatson Institute, Glasgow, United Kingdom.
Cancer Research UK Scotland Institute · GB

Funding

Cancer Research UK 23983Cancer Research UK A23983Cancer Research UK A25142Cancer Research UK A31287
6 · The paper itself

Abstract

The tumor microenvironment profoundly influences the behavior of recruited leukocytes and tissue-resident immune cells. These immune cells, which inherently have environmentally driven plasticity necessary for their roles in tissue homeostasis, dynamically interact with tumor cells and the tumor stroma and play critical roles in determining the course of disease. Among these immune cells, neutrophils were once considered much more static within the tumor microenvironment; however, some of these earlier assumptions were the product of the notorious difficulty in manipulating neutrophils in vitro. Technological advances that allow us to study neutrophils in context are now revealing the true roles of neutrophils in the tumor microenvironment. Here we discuss recent data generated by some of these tools and how these data might be synthesized into more elegant ways of targeting these powerful and abundant effector immune cells in the clinic.

Indexed as

AnimalsDisease ProgressionHumansImmunotherapyModels, ImmunologicalNeoplasm MetastasisNeoplasmsNeutropeniaNeutrophilsTranslational Research, BiomedicalTumor Microenvironment

Identifiers

PMID33720040
PMCPMC7954585
OpenAlexW3137657187

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.