Evidence map›Paper›PMID 36612268›Full record

ArticleCancers2022

Macrophage Resistance to Ionizing Radiation Exposure Is Accompanied by Decreased Cathepsin D and Increased Transferrin Receptor 1 Expression.

Ana Teresa Pinto, Ana Beatriz Machado, Hugo Osório, Marta Laranjeiro Pinto, Rui Vitorino, Gonçalo Justino, Cátia Santa, Flávia Castro, Tânia Cruz, Carla Rodrigues and 13 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
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

23 authors at 9 institutions in 3 countries.

Ana Teresa Pintoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0003-0974-2206
Ana Beatriz Machadoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-7559-7599
Hugo Osórioi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-6362-8255
Marta Laranjeiro Pintoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Rui VitorinoDepartment of Medical Sciences, Institute of Biomedicine (iBiMED), Universidade de Aveiro, 3810-193 Aveiro, Portugal.ORCID 0000-0003-3636-5805
Gonçalo JustinoCentro de Química Estrutural-Institute of Molecular Sciences, Instituto Superior Técnico, Universidade Técnica de Lisboa, 1049-001 Lisboa, Portugal.ORCID 0000-0003-4828-4738
Cátia SantaCNC-Center for Neuroscience and Cell Biology, Universidade de Coimbra, 3004-504 Coimbra, Portugal.
Flávia Castroi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-2273-2806
Tânia Cruzi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Carla RodriguesREQUIMTE-LAQV, Chemistry Department, NOVA School of Science and Technology, Universidade de Lisboa, 2829-516 Caparica, Portugal.
Jorge Limai3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
José Luís R SousaPersonal Health Data Science Group, Sano-Centre for Computational Personalised Medicine, 30-054 Krakow, Poland.
Ana Patrícia Cardosoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0003-1987-0316
Rita FigueiraRadiotherapy Service, Centro Hospitalar Universitário São João (CHUSJ), EPE, 4200-319 Porto, Portugal.
Armanda MonteiroRadiotherapy Service, Centro Hospitalar Universitário São João (CHUSJ), EPE, 4200-319 Porto, Portugal.
Margarida MarquesRadiotherapy Service, Centro Hospitalar Universitário São João (CHUSJ), EPE, 4200-319 Porto, Portugal.ORCID 0000-0002-9636-0443
Bruno ManadasInstitute for Interdisciplinary Research (III), Universidade de Coimbra, 3030-789 Coimbra, Portugal.ORCID 0000-0002-2087-4042
Jarne PauwelsVIB-UGent Center for Medical Biotechnology, 9052 Ghent, Belgium.ORCID 0000-0002-8525-7109
Kris GevaertVIB-UGent Center for Medical Biotechnology, 9052 Ghent, Belgium.ORCID 0000-0002-4237-0283
Marc MareelDepartment of Radiation Oncology and Experimental Cancer Research, Ghent University Hospital, 9000 Ghent, Belgium.
Sónia RochaInstitute of System, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3 GE, UK.ORCID 0000-0002-2413-4981
Tiago Duartei3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Maria José Oliveirai3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-0724-0272
Universidade do Porto · PTHospital de São João · PTGhent University · BEUniversity of Coimbra · PTChampalimaud Foundation · PTGhent University Hospital · BEUniversity of Aveiro · PTUniversity of Lisbon · PTUniversity of Liverpool · GB

Funding

Wellcome Trust 206293/Z/17/Z
6 · The paper itself

Abstract

purposeTo identify a molecular signature of macrophages exposed to clinically relevant ionizing radiation (IR) doses, mirroring radiotherapy sessions.

methodsHuman monocyte-derived macrophages were exposed to 2 Gy/ fraction/ day for 5 days, mimicking one week of cancer patient's radiotherapy. Protein expression profile by proteomics was performed.

resultsA gene ontology analysis revealed that radiation-induced protein changes are associated with metabolic alterations, which were further supported by a reduction of both cellular ATP levels and glucose uptake. Most of the radiation-induced deregulated targets exhibited a decreased expression, as was the case of cathepsin D, a lysosomal protease associated with cell death, which was validated by Western blot. We also found that irradiated macrophages exhibited an increased expression of the transferrin receptor 1 (TfR1), which is responsible for the uptake of transferrin-bound iron. TfR1 upregulation was also found in tumor-associated mouse macrophages upon tumor irradiation. In vitro irradiated macrophages also presented a trend for increased divalent metal transporter 1 (DMT1), which transports iron from the endosome to the cytosol, and a significant increase in iron release.

conclusionsIrradiated macrophages present lower ATP levels and glucose uptake, and exhibit decreased cathepsin D expression, while increasing TfR1 expression and altering iron metabolism.

Indexed as

cathepsin Dionizing radiationiron metabolismmacrophagesproteomicsradiotherapytransferrin receptor 1 (TfR1)

Identifiers

PMID36612268
PMCPMC9818572
OpenAlexW4313388821

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.