Evidence map›Paper›PMID 24466382›Full record

ArticleTranslational oncology2013

CCR5 Antagonism by Maraviroc Reduces the Potential for Gastric Cancer Cell Dissemination.

Andrea Mencarelli, Luigina Graziosi, Barbara Renga, Sabrina Cipriani, Claudio D'Amore, Daniela Francisci, Angela Bruno, Franco Baldelli, Annibale Donini, Stefano Fiorucci

Open access · goldAbstract read
In one paragraph

Article in Translational oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

32 citing papers in PubMed, 54 citations in OpenAlex.

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  5. Inflammatory factors collaboratively linkFrontiers in immunology · 2025
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  20. Inhibition of the CCL5/CCR5 Axis against the Progression of Gastric Cancer.International journal of molecular sciences · 2018
    Review
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

10 authors at 1 institution in 1 country.

Andrea MencarelliDipartimento di Medicina Clinica e Sperimentale, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Luigina GraziosiDipartimento di Scienze Chirurgiche, Radiologiche e Odontostomatologiche, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Barbara RengaDipartimento di Medicina Clinica e Sperimentale, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Sabrina CiprianiDipartimento di Medicina Clinica e Sperimentale, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Claudio D'AmoreDipartimento di Medicina Clinica e Sperimentale, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Daniela FrancisciDipartimento di Medicina Generale e Scienze Biochimiche, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Angela BrunoDipartimento di Medicina Clinica e Sperimentale, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Franco BaldelliDipartimento di Medicina Generale e Scienze Biochimiche, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Annibale DoniniDipartimento di Scienze Chirurgiche, Radiologiche e Odontostomatologiche, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
Stefano FiorucciDipartimento di Medicina Clinica e Sperimentale, Nuova Facoltà di Medicina e Chirurgia, Università di Perugia, Perugia, Italy.
University of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chemokine (C-C motif) receptor 5 (CCR5) that belongs to the family of G protein-coupled receptors is exploited by macrophage tropic (R5) human immunodeficiency virus type 1 (HIV-1) to enter cells. Maraviroc, a small molecule CCR antagonist, is used as a part of combination antiretroviral therapy to treat persons infected by R5 HIV-1. CCR5 is expressed in various cancers, and its level of expression is a negative predictor of patients' survival in gastric cancers. Here, we report MKN45, MKN74, and KATOIII cells, three human gastric cancer cell lines with different stages of differentiation, which express CCR5 as detected by flow cytometry and reverse transcription-polymerase chain reaction (RT-PCR), and its ligand RANTES. In vitro experiments demonstrate that CCR5 antagonism reduces gastric cancer cell migration induced by macrophage inflammatory protein 1α (MIP-1α), MIP-1β, and RANTES and adhesion to the ex-planted murine peritoneum. Administration of maraviroc from days 3 to 10 after MKN45 cell inoculation to severe combined immunodeficient (SCID) mice effectively reduced the extent of peritoneal disease and increased survival. Maraviroc treatment also reduced the tumor burden in a xenograft model. Gene expression and RT-PCR analyses revealed that CCR5 antagonism in vivo modulates the expression of genes known for their role in cancer growth including interleukin-10 receptor B; hepatocyte growth factor receptor (MET); the homolog of the atypical cadherin gene, FAT1; Nm23-H1; and lymphotoxin β receptor. In summary, we have shown that CCR5 is mechanistically involved in dissemination of gastric cancer cells, suggesting that small molecule inhibitors of CCR5 might be exploited for their anticancer potential.

Identifiers

PMID24466382
PMCPMC3890714
OpenAlexW2102054577

What OpenQuestion holds

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Registered trials

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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.