Evidence map›Paper›PMID 32694624›Full record

ReviewNature reviews. Cancer2020

Neutrophil diversity and plasticity in tumour progression and therapy.

Sebastien Jaillon, Andrea Ponzetta, Diletta Di Mitri, Angela Santoni, Raffaella Bonecchi, Alberto Mantovani

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 834 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
834citing papers in PubMed, 5 pooled it
47.3field-weighted citation impact, top 1% 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

834 citing papers in PubMed, 5 syntheses or guidelines pooled it, 1,272 citations in OpenAlex.

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  16. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  17. Article
  18. Review
  19. Neutrophils in cancer.Nature reviews. Cancer · 2026
    Review
  20. Article

774 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

6 authors at 2 institutions in 2 countries.

Sebastien JaillonDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy. sebastien.jaillon@humanitasresearch.it.
Andrea PonzettaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.ORCID http://orcid.org/0000-0003-3224-802X
Diletta Di MitriHumanitas Clinical and Research Center IRCCS, Rozzano (MI), Italy.
Angela SantoniDipartimento di Medicina Molecolare Istituto Pasteur-Fondazione Cenci Bolognetti, Università di Roma 'La Sapienza', Rome, Italy.
Raffaella BonecchiDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Alberto MantovaniDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy. alberto.mantovani@humanitasresearch.it.ORCID http://orcid.org/0000-0001-5578-236X
Humanitas University · ITIstituto Neurologico Mediterraneo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils play a key role in defence against infection and in the activation and regulation of innate and adaptive immunity. In cancer, tumour-associated neutrophils (TANs) have emerged as an important component of the tumour microenvironment. Here, they can exert dual functions. TANs can be part of tumour-promoting inflammation by driving angiogenesis, extracellular matrix remodelling, metastasis and immunosuppression. Conversely, neutrophils can also mediate antitumour responses by direct killing of tumour cells and by participating in cellular networks that mediate antitumour resistance. Neutrophil diversity and plasticity underlie the dual potential of TANs in the tumour microenvironment. Myeloid checkpoints as well as the tumour and tissue contexture shape neutrophil function in response to conventional therapies and immunotherapy. We surmise that neutrophils can provide tools to tailor current immunotherapy strategies and pave the way to myeloid cell-centred therapeutic strategies, which would be complementary to current approaches.

Indexed as

AnimalsHumansImmunotherapyNeoplasmsNeoplastic ProcessesNeutrophilsTumor Microenvironment

Identifiers

PMID32694624
OpenAlexW3044222890

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.