Evidence map›Paper›PMID 40050933›Full record

ReviewMolecular cancer2025

Harnessing myeloid cells in cancer.

Su-Yeon Park, Ekaterina Pylaeva, Vikas Bhuria, Adriana Rosa Gambardella, Giovanna Schiavoni, Dimitrios Mougiakakos, Sung-Hoon Kim, Jadwiga Jablonska

Abstract readReview
In one paragraph

Review in Molecular cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Gut microbiota in health and disease.Molecular biomedicine · 2026
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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

8 authors.

Su-Yeon ParkCancer Molecular Target Herbal Research Lab, College of Korean Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
Ekaterina PylaevaDepartment of Otorhinolaryngology, University Hospital Essen, University Duisburg-Essen, Hufelandstraße 55, Essen, 45147, Germany.
Vikas BhuriaDepartment of Hematology, Oncology, and Cell Therapy, Otto-Von-Guericke University, Magdeburg, Germany.
Adriana Rosa GambardellaDepartment of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy.
Giovanna SchiavoniDepartment of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy.
Dimitrios MougiakakosDepartment of Hematology, Oncology, and Cell Therapy, Otto-Von-Guericke University, Magdeburg, Germany.
Sung-Hoon KimCancer Molecular Target Herbal Research Lab, College of Korean Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
Jadwiga JablonskaDepartment of Otorhinolaryngology, University Hospital Essen, University Duisburg-Essen, Hufelandstraße 55, Essen, 45147, Germany. jadwiga.jablonska@uk-essen.de.

Funding

Deutsche Forschungsgemeinschaft 536993790Deutsche Forschungsgemeinschaft CRC TRR332 project A05European Regional Development Fund ZELL-THEMAFondazione AIRC per la ricerca sul cancro ETS N 21366National Research Foundation of Korea 2021R1A2C2003277
6 · The paper itself

Abstract

Cancer-associated myeloid cells due to their plasticity play dual roles in both promoting and inhibiting tumor progression. Myeloid cells with immunosuppressive properties play a critical role in anti-cancer immune regulation. Cells of different origin, such as tumor associated macrophages (TAMs), tumor associated neutrophils (TANs), myeloid derived suppressor cells (also called MDSCs) and eosinophils are often expanded in cancer patients and significantly influence their survival, but also the outcome of anti-cancer therapies. For this reason, the variety of preclinical and clinical studies to modulate the activity of these cells have been conducted, however without successful outcome to date. In this review, pro-tumor activity of myeloid cells, myeloid cell-specific therapeutic targets, in vivo studies on myeloid cell re-polarization and the impact of myeloid cells on immunotherapies/genetic engineering are addressed. This paper also summarizes ongoing clinical trials and the concept of chimeric antigen receptor macrophage (CAR-M) therapies, and suggests future research perspectives, offering new opportunities in the development of novel clinical treatment strategies.

Indexed as

Myeloid CellsNeoplasmsAnimalsHumansImmunotherapyMyeloid-Derived Suppressor CellsTumor MicroenvironmentEosinophilsImmunosuppressionMacrophagesMyeloid cellsNeutrophilsTherapeutic target

Identifiers

PMID40050933
PMCPMC11887392

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.