Evidence map›Paper›PMID 31982939›Full record

ArticleCancer immunology, immunotherapy : CII2020

NETosis in cancer: a critical analysis of the impact of cancer on neutrophil extracellular trap (NET) release in lung cancer patients vs. mice.

Ludovica Arpinati, Merav E Shaul, Naomi Kaisar-Iluz, Shira Mali, Sojod Mahroum, Zvi G Fridlender

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 56 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Ludovica ArpinatiInstitute of Pulmonary Medicine, Hebrew University Hadassah Medical Center, POB 12000, 9112001, Jerusalem, Israel.
Merav E ShaulInstitute of Pulmonary Medicine, Hebrew University Hadassah Medical Center, POB 12000, 9112001, Jerusalem, Israel.
Naomi Kaisar-IluzInstitute of Pulmonary Medicine, Hebrew University Hadassah Medical Center, POB 12000, 9112001, Jerusalem, Israel.
Shira MaliInstitute of Pulmonary Medicine, Hebrew University Hadassah Medical Center, POB 12000, 9112001, Jerusalem, Israel.
Sojod MahroumInstitute of Pulmonary Medicine, Hebrew University Hadassah Medical Center, POB 12000, 9112001, Jerusalem, Israel.
Zvi G FridlenderInstitute of Pulmonary Medicine, Hebrew University Hadassah Medical Center, POB 12000, 9112001, Jerusalem, Israel. fridlender@hadassah.org.il.ORCID http://orcid.org/0000-0002-6122-1988
Hadassah Medical Center · IL

Funding

DKFZ-MOST Cooperation in Cancer Research 2656Israel Lung Association N/ANaor Sasson Fund N/A
6 · The paper itself

Abstract

Neutrophils play a major role in tumor biology. Among other functions, neutrophils can release extracellular traps (NETs), mesh-like structures of decondensed chromatin fibers, in a process termed NETosis. Originally characterized as an antimicrobial mechanism, NETosis has been described in cancer, but cancer-related predisposition is not clear. In the current study, we investigated the predisposition of circulating neutrophils to release NETs in lung cancer and the impact of G-CSF on this function, comparing circulating neutrophils isolated from cancer patients to the LLC and AB12 mouse models. We find that neutrophils from both healthy donors and cancer patients display high NETotic potential, with 30-60% of cells undergoing NETosis upon PMA stimulation. In contrast, neutrophils isolated from tumor-bearing mice displayed only 4-5% NETotic cells, though significantly higher than naive controls (1-2%). Despite differential mechanisms of activation described, Ionomycin and PMA mainly triggered suicidal rather than vital NETosis. G-CSF secreting tumors did not increase NETotic rates in murine neutrophils, and direct G-CSF stimulation did not promote their NET release. In contrast, human neutrophils strongly responded to G-CSF stimulation resulting also in a higher response to PMA + G-CSF stimulation. Our data show clear differences in NETotic potentials between human and murine neutrophils. We do not find a predisposition of neutrophils to release NETs in lung cancer patients compared to healthy controls, whereas cancer may modulate neutrophils' NETotic potential in mice. G-CSF secreted from tumors differentially affects murine and human NETosis in cancer. These important differences should be considered in future studies of NETosis in cancer.

Indexed as

AnimalsCell Line, TumorExtracellular TrapsGranulocyte Colony-Stimulating FactorHumansIonomycinLung NeoplasmsMiceMice, Inbred BALB CMice, Inbred C57BLNeutrophilsTetradecanoylphorbol AcetateGranulocyte Colony-Stimulating FactorIonomycinTetradecanoylphorbol AcetateCITIM 2019G-CSFLung cancerNetosisNeutrophils

Identifiers

PMID31982939
PMCPMC11027875
OpenAlexW3004466456

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.