Evidence map›Paper›PMID 36257966›Full record

ArticleNature communications2022

Reprogramming of myeloid cells and their progenitors in patients with non-medullary thyroid carcinoma.

Katrin Rabold, Martijn Zoodsma, Inge Grondman, Yunus Kuijpers, Manita Bremmers, Martin Jaeger, Bowen Zhang, Willemijn Hobo, Han J Bonenkamp, Johannes H W de Wilt and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 18 citations in OpenAlex.

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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

20 authors at 4 institutions in 3 countries.

Katrin Rabold *Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Martijn Zoodsma *Department of Computational Biology for Individualised Infection Medicine, Centre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and the Hannover Medical School (MHH), Hannover, Germany.ORCID 0000-0003-3636-2209
Inge GrondmanDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Yunus KuijpersDepartment of Computational Biology for Individualised Infection Medicine, Centre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and the Hannover Medical School (MHH), Hannover, Germany.ORCID 0000-0002-5075-3970
Manita BremmersDepartment of Haematology, Radboud University Medical Center, Nijmegen, The Netherlands.
Martin JaegerDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Bowen ZhangDepartment of Computational Biology for Individualised Infection Medicine, Centre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and the Hannover Medical School (MHH), Hannover, Germany.
Willemijn HoboDepartment of Laboratory Medicine, Laboratory of Hematology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Han J BonenkampDepartment of Surgery, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Johannes H W de WiltDepartment of Surgery, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.ORCID 0000-0001-6773-9668
Marcel J R JanssenDepartment of Radiology and Nuclear Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Lenneke A M CornelissenRadiotherapy and OncoImmunology Laboratory, Department of Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
Ilse C H van Engen-van GrunsvenDepartment of Pathology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Willem J M MulderBiomedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, USA.ORCID 0000-0001-8665-3878
Jan W A SmitDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, The Netherlands.
Gosse J AdemaRadiotherapy and OncoImmunology Laboratory, Department of Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-6750-1665
Mihai G NeteaDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0003-2421-6052
Yang LiDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0003-4022-7341
Cheng-Jian XuDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands. xu.chengjian@mh-hannover.de.
Romana T Netea-MaierDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, The Netherlands. romana.netea-maier@radboudumc.nl.ORCID 0000-0002-9603-0460
Radboud University Nijmegen · NLMedizinische Hochschule Hannover · DEAmsterdam University Medical Centers · NLUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid cells, crucial players in antitumoral defense, are affected by tumor-derived factors and treatment. The role of myeloid cells and their progenitors prior to tumor infiltration is poorly understood. Here we show single-cell transcriptomics and functional analyses of the myeloid cell lineage in patients with non-medullary thyroid carcinoma (TC) and multinodular goiter, before and after treatment with radioactive iodine compared to healthy controls. Integrative data analysis indicates that monocytes of TC patients have transcriptional upregulation of antigen presentation, reduced cytokine production capacity, and overproduction of reactive oxygen species. Interestingly, these cancer-related pathological changes are partially removed upon treatment. In bone marrow, TC patients tend to shift from myelopoiesis towards lymphopoiesis, reflected in transcriptional differences. Taken together, distinct transcriptional and functional changes in myeloid cells arise before their infiltration of the tumor and are already initiated in bone marrow, which suggests an active role in forming the tumor immune microenvironment.

Indexed as

Iodine RadioisotopesThyroid NeoplasmsCytokinesHumansMyeloid CellsMyelopoiesisReactive Oxygen SpeciesTumor MicroenvironmentCytokinesIodine RadioisotopesReactive Oxygen Species

Identifiers

PMID36257966
PMCPMC9579179
OpenAlexW4306670856

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.