Evidence map›Paper›PMID 24591756›Full record

ReviewDisease markers2014

CC chemokine receptor 5: the interface of host immunity and cancer.

Carlos Eduardo Coral de Oliveira, Julie Massayo Maeda Oda, Roberta Losi Guembarovski, Karen Brajão de Oliveira, Carolina Batista Ariza, Jamil Soni Neto, Bruna Karina Banin Hirata, Maria Angelica Ehara Watanabe

Open access · hybridAbstract readReview
In one paragraph

Review in Disease markers, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 62 citations in OpenAlex.

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  15. Evaluating the Association betweenIranian journal of public health · 2021
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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 at 1 institution in 1 country.

Carlos Eduardo Coral de OliveiraLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Julie Massayo Maeda OdaLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Roberta Losi GuembarovskiLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Karen Brajão de OliveiraLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Carolina Batista ArizaLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Jamil Soni NetoLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Bruna Karina Banin HirataLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Maria Angelica Ehara WatanabeLaboratory of Polymorphism and Application Study of DNA, Department of Pathological Sciences, Biological Sciences Center, State University of Londrina, Celso Garcia Cid highway, Pr 445, Km 380, 86057-970 Londrina, PR, Brazil.
Universidade Estadual de Londrina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid tumors are embedded in a stromal microenvironment consisting of immune cells, such as macrophages and lymphocytes, as well as nonimmune cells, such as endothelial cells and fibroblasts. Chemokines are a type of small secreted chemotactic cytokine and together with their receptors play key roles in the immune defense. Critically, they regulate cancer cellular migration and also contribute to their proliferation and survival. The CCR5 chemokine receptor is involved in leucocytes chemotaxis to sites of inflammation and plays an important role in the macrophages, T cells, and monocytes recruitment. Additionally, CCR5 may have an indirect effect on cancer progression by controlling the antitumor immune response, since it has been demonstrated that its expression could promote tumor growth and contribute to tumor metastasis, in different types of malignant tumors. Furthermore, it was demonstrated that a CCR5 antagonist may inhibit tumor growth, consisting of a possible therapeutic target. In this context, the present review focuses on the establishment of CCR5 within the interface of host immunity, tumor microenvironment, and its potential as a targeting to immunotherapy.

Indexed as

AnimalsChemokine CCL5HumansImmunotherapyNeoplasmsReceptors, CCR5Signal TransductionT-Lymphocytes, RegulatoryTumor MicroenvironmentCCL5 protein, humanCCR5 protein, humanChemokine CCL5Receptors, CCR5

Identifiers

PMID24591756
PMCPMC3925608
OpenAlexW2019459590

What OpenQuestion holds

Textmetadata
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.