Evidence map›Paper›PMID 27513864›Full record

ArticlePloS one2016

Intricate Macrophage-Colorectal Cancer Cell Communication in Response to Radiation.

Ana T Pinto, Marta L Pinto, Sérgia Velho, Marta T Pinto, Ana P Cardoso, Rita Figueira, Armanda Monteiro, Margarida Marques, Raquel Seruca, Mário A Barbosa and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. 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
2.8field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Modulation of tumor-associated macrophage activity with radiation therapy: a systematic review.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2023
    Pooled it
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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

13 authors at 4 institutions in 3 countries.

Ana T Pintoi3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Marta L Pintoi3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Sérgia Velhoi3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Marta T Pintoi3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Ana P Cardosoi3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Rita FigueiraRadiotherapy Service, Centro Hospitalar S. João, EPE, Porto, Portugal.
Armanda MonteiroRadiotherapy Service, Centro Hospitalar S. João, EPE, Porto, Portugal.
Margarida MarquesRadiotherapy Service, Centro Hospitalar S. João, EPE, Porto, Portugal.
Raquel Serucai3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Mário A Barbosai3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Marc MareelDepartment of Radiation Oncology and Experimental Cancer Research, Ghent University Hospital, Ghent, Belgium.
Maria J Oliveirai3s-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Sónia RochaCentre for Gene Regulation and Expression, College of Life Sciences, University of Dundee, Dundee, United Kingdom.
i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTUniversidade do Porto · PTGhent University Hospital · BEUniversity of Dundee · GB

Funding

Cancer Research UK 12918Wellcome Trust
6 · The paper itself

Abstract

Both cancer and tumour-associated host cells are exposed to ionizing radiation when a tumour is subjected to radiotherapy. Macrophages frequently constitute the most abundant tumour-associated immune population, playing a role in tumour progression and response to therapy. The present work aimed to evaluate the importance of macrophage-cancer cell communication in the cellular response to radiation. To address this question, we established monocultures and indirect co-cultures of human monocyte-derived macrophages with RKO or SW1463 colorectal cancer cells, which exhibit higher and lower radiation sensitivity, respectively. Mono- and co-cultures were then irradiated with 5 cumulative doses, in a similar fractionated scheme to that used during cancer patients' treatment (2 Gy/fraction/day). Our results demonstrated that macrophages sensitize RKO to radiation-induced apoptosis, while protecting SW1463 cells. Additionally, the co-culture with macrophages increased the mRNA expression of metabolism- and survival-related genes more in SW1463 than in RKO. The presence of macrophages also upregulated glucose transporter 1 expression in irradiated SW1463, but not in RKO cells. In addition, the influence of cancer cells on the expression of pro- and anti-inflammatory macrophage markers, upon radiation exposure, was also evaluated. In the presence of RKO or SW1463, irradiated macrophages exhibit higher levels of pro-inflammatory TNF, IL6, CCL2 and CCR7, and of anti-inflammatory CCL18. However, RKO cells induce an increase of macrophage pro-inflammatory IL1B, while SW1463 cells promote higher pro-inflammatory CXCL8 and CD80, and also anti-inflammatory VCAN and IL10 levels. Thus, our data demonstrated that macrophages and cancer cells mutually influence their response to radiation. Notably, conditioned medium from irradiated co-cultures increased non-irradiated RKO cell migration and invasion and did not impact on angiogenesis in a chicken embryo chorioallantoic membrane assay. Overall, the establishment of primary human macrophage-cancer cell co-cultures revealed an intricate cell communication in response to ionizing radiation, which should be considered when developing therapies adjuvant to radiotherapy.

Indexed as

AnimalsCell CommunicationCell Line, TumorChick EmbryoCoculture TechniquesColorectal NeoplasmsGlucose Transport Proteins, FacilitativeHumansMacrophagesNeoplasm InvasivenessGlucose Transport Proteins, Facilitative

Identifiers

PMID27513864
PMCPMC4981353
OpenAlexW2510984681

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.