Evidence map›Paper›PMID 41373493›Full record

ArticleInternational journal of molecular sciences2025

High Local and Systemic Expression of Pentraxin-3 in Anaplastic Thyroid Cancer.

Andreea Bojoga, Pepijn van Houten, Martin Jaeger, Katrin Rabold, Birgitte Walgreen, Liesbeth van Emst, Dumitru Ioachim, Ilse van Engen-van Grunsven, Corin Badiu, Romana T Netea-Maier

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

10 authors.

Andreea BojogaFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.ORCID 0000-0002-6883-2378
Pepijn van HoutenDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.ORCID 0000-0002-8503-4140
Martin JaegerDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.ORCID 0000-0001-6994-493X
Katrin RaboldDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Birgitte WalgreenRheumatology Research Laboratory, Department of Internal Medicine, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Liesbeth van EmstDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Dumitru IoachimDepartment of Pathology, National Institute of Endocrinology C. I. Parhon, 011863 Bucharest, Romania.
Ilse van Engen-van GrunsvenDepartment of Pathology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Corin BadiuFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.ORCID 0000-0002-8087-8125
Romana T Netea-MaierDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.ORCID 0000-0002-9603-0460

Funding

European Joint Programme for Rare Disease under Research mobility grant EJP WP 17Next Generation EU: Program of National Recovery and Resilience grant: Decoding the im-mune-inflammatory axis in rare non-medullary thyroid cancer as an innovative approach for novel combinatory therapeutic approaches Code:81/15.11.2022; Contract 760067/23/5.2023
6 · The paper itself

Abstract

Chronic inflammation plays a key role in cancer pathogenesis. Aggressive thyroid cancer is associated with immune infiltration and systemic inflammation. Long pentraxin 3 (PTX3) is an inflammatory protein implicated in tumor progression. This study evaluates PTX3 plasma levels in patients with non-medullary thyroid cancer (TC) compared to benign thyroid disease and investigates its tissue expression. We prospectively included 55 TC patients: 42 papillary, 3 follicular, 4 oncocytic, 4 anaplastic (ATC), and 2 poorly differentiated (PDTC). The control group consisted of 32 patients with benign thyroid disease. PTX3 plasma concentrations were measured by ELISA, and tissue expression of PTX3 and CD68 was analyzed using immunohistochemistry. PTX3 plasma levels did not significantly differ between TC and controls, but patients with PDTC and ATC had markedly higher concentrations. Tissue analysis showed strong PTX3 expression in three of four ATC cases in tumor and stromal cells, whereas benign and differentiated thyroid tissues exhibited minimal staining. CD68 expression was positive in ATC, indicating tumor-associated macrophage infiltration, but a few cells were double-positive for PTX3 and CD68. Our findings suggest a possible association between PTX3 and aggressive TC, particularly ATC. Further studies are needed to validate these findings and elucidate the cellular origin and functional role of PTX3.

Indexed as

C-Reactive ProteinSerum Amyloid P-ComponentThyroid Carcinoma, AnaplasticThyroid NeoplasmsAdultAgedAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkers, TumorCD68 MoleculeFemaleHumansImmunohistochemistryMaleMiddle AgedPentraxinsAntigens, CDAntigens, Differentiation, MyelomonocyticBiomarkers, TumorCD68 antigen, humanCD68 MoleculeC-Reactive ProteinPentraxinsSerum Amyloid P-Componentanaplastic thyroid cancernon-medullary thyroid cancerpentraxin 3tumor-associated inflammation

Identifiers

PMID41373493
PMCPMC12692025

What Socratic 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 Socratic graph.