Evidence map›Paper›PMID 30894861›Full record

ReviewFrontiers in immunology2019

Chemokines and Chemokine Receptors: New Targets for Cancer Immunotherapy.

Valeria Mollica Poeta, Matteo Massara, Arianna Capucetti, Raffaella Bonecchi

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 350 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
350citing papers in PubMed, 2 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

350 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  12. Structure basis for C-C chemokine receptor 4 modulation by orthosteric and allosteric antagonists.Proceedings of the National Academy of Sciences of the United States of America · 2026
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290 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.

Valeria Mollica PoetaHumanitas Clinical and Research Center, IRCCS, Rozzano, Italy.
Matteo MassaraHumanitas Clinical and Research Center, IRCCS, Rozzano, Italy.
Arianna CapucettiHumanitas Clinical and Research Center, IRCCS, Rozzano, Italy.
Raffaella BonecchiHumanitas Clinical and Research Center, IRCCS, Rozzano, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy is a clinically validated treatment for many cancers to boost the immune system against tumor growth and dissemination. Several strategies are used to harness immune cells: monoclonal antibodies against tumor antigens, immune checkpoint inhibitors, vaccination, adoptive cell therapies (e.g., CAR-T cells) and cytokine administration. In the last decades, it is emerging that the chemokine system represents a potential target for immunotherapy. Chemokines, a large family of cytokines with chemotactic activity, and their cognate receptors are expressed by both cancer and stromal cells. Their altered expression in malignancies dictates leukocyte recruitment and activation, angiogenesis, cancer cell proliferation, and metastasis in all the stages of the disease. Here, we review first attempts to inhibit the chemokine system in cancer as a monotherapy or in combination with canonical or immuno-mediated therapies. We also provide recent findings about the role in cancer of atypical chemokine receptors that could become future targets for immunotherapy.

Indexed as

Antibodies, Monoclonal, HumanizedBenzylaminesChemokines, CCChemokines, CXCCyclamsHeterocyclic CompoundsHumansImmunotherapyMolecular Targeted TherapyNeoplasmsReceptors, CCRReceptors, CXCRAntibodies, Monoclonal, HumanizedBenzylaminesChemokines, CCChemokines, CXCCyclamsHeterocyclic CompoundsmogamulizumabplerixaforReceptors, CCRReceptors, CXCRatypical chemokine receptorcancer related inflammationchemokinechemokine receptorimmunotherapy

Identifiers

PMID30894861
PMCPMC6414456

What OpenQuestion holds

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LicenceCC BY
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.